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Chemical compound
Decalin (decahydronaphthalene, also known as bicyclo[4.4.0]decane and sometimes decaline), a bicyclic organic compound, is an industrial solvent. A colorless
Decalin
Chemical compound
metal catalysts to give tetralin (C10H12). Further hydrogenation yields decalin (C10H18). Oxidation with O2 in the presence of vanadium pentoxide (V2O5)
Naphthalene
Chemical compound
Perfluorodecalin (C10F18) is a fluorocarbon, a derivative of decalin in which all of the hydrogen atoms are replaced by fluorine atoms. It is chemically
Perfluorodecalin
Very long-chain polyethylene with high impact strength
In the case where decalin is used, the decalin is left to evaporate from the yarn. When producing at industrial levels, this decalin can be recovered and
Ultra-high-molecular-weight polyethylene
Ultra-high-molecular-weight_polyethylene
Molecule with two joined rings
elements), like DABCO. Moreover, the two rings can both be aliphatic (e.g. decalin and norbornane), or can be aromatic (e.g. naphthalene), or a combination
Bicyclic_molecule
Chemical compound responsible for the characteristic odour of earth
disturbed. Geosmin is a bicyclic alcohol with formula C12H22O, a derivative of decalin. It is produced from the universal sesquiterpene precursor farnesyl pyrophosphate
Geosmin
Chemical compound
evaluated. Over-hydrogenation converts tetralin into decahydronaphthalene (decalin). Rarely encountered is dihydronaphthalene (dialin). In a classic named
Tetralin
Chemical species structure notation
O1CCOCC1 respectively. For a second ring, the label will be 2. For example, decalin (decahydronaphthalene) may be written as C1CCCC2C1CCCC2. SMILES does not
Simplified Molecular Input Line Entry System
Simplified_Molecular_Input_Line_Entry_System
Class of chemical compounds
marine sponges. They are bicyclic terpenes that contain 20 carbons and a decalin core. The clerodane diterpenes are classified into four groups trans-cis
Clerodane_diterpene
Chemical reaction involving organic compounds
titanium tetrachloride in dichloromethane at −78 °C gives access to the decalin skeleton with the hydroxyl group and chlorine group predominantly in cis
Prins_reaction
Chemical compound
dehydration of 1,2,3,4-tetrahydro-1-naphthol [wd]. Naphthalene Tetralin Decalin 1,4-Dihydronaphthalene (registry number 612-17-9), an isomer of 1,2-Dihydronaphthalene
Dialin
Organic molecule with one or more non-aromatic all-carbon rings
cyclohexane, cycloheptane, cyclooctane, and so on. Bicyclic alkanes include decalin, housane, and norbornane. Polycyclic alkanes include cubane, basketane
Alicyclic_compound
German chemist (born 1964)
London with a thesis on preparative organic chemistry (Synthesis of the decalin fragment of azadirachtin). As a postdoctoral fellow he worked with Barry
Hartmuth_C._Kolb
Hydrocarbon compound (C6H6)
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Benzene
Chemical compound
24 steps to yield salvinorin A in 0.15% yield. An approach to the trans-decalin ring system of salvinorin A used an intramolecular Diels-Alder reaction/Tsuji
Salvinorin_A
Compound containing rings with delocalized pi electrons
saturated rings. The compound 1-naphthol is completely reduced to a mixture of decalin-ol isomers. The compound resorcinol, hydrogenated with Raney nickel in
Aromatic_compound
Thermoplastic polymer
PP can be dissolved in nonpolar solvents such as xylene, tetralin and decalin. Due to the tertiary carbon atom, PP is chemically less resistant than
Polypropylene
Organic compound consisting entirely of hydrogen and carbon
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Hydrocarbon
Chemical compound
oil. Octanol and glycerin are byproducts. It can also be obtained from decalin via the a hydroperoxide, which rearranges to give a hydroxycyclodecanone
Sebacic_acid
Chemical compound
I polyketide synthase (PKS) and an amino acid biogenetic pathway. The decalin moiety is attributed to PKS using acetyl-CoA, malonyl-CoA, methylmalonyl-CoA
Conipyridoin_E
Index of chemical compounds with the same molecular formula
The molecular formula C10H18 may refer to: Bornane Cyclodecene Decalin Decynes 1-Decyne 2-Decyne 3-Decyne 4-Decyne 5-Decyne, also known as dibutylethyne
C10H18
Chemical compound
1967 publication relied on an intramolecular aldol condensation of a cis-decalin ketol. It is formed when basketane is hydrogenated. [dubious – discuss]
Twistane
Chemical compound
synthesis was a relay approach, with the required, heavily functionalized decalin intermediate being made by total synthesis on a small scale, but being
Azadirachtin
Chemical compound
Andrographolide is a labdane diterpenoid that has been isolated from the stem and leaves of Andrographis paniculata. Andrographolide is an extremely bitter
Andrographolide
Chemical compound
Ambroxide, widely known by the brand name Ambroxan, is a naturally occurring terpenoid and one of the key constituents responsible for the odor of ambergris
Ambroxide
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Styrene
Methoxyphenol compound, constituent of plant lignins and essential oils
strategy in organic synthesis: Short and efficient construction of cis-decalins and linear triquinanes from 2-methoxyphenols". Pure and Applied Chemistry
Guaiacol
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Azulene
Organic compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Cumene
Natural organic compounds derived from a [C(O)–CH2] chain
subclasses of polyketides including: aromatics, macrolactones/macrolides, decalin ring containing, polyether, and polyenes. Polyketide synthases are also
Polyketide
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Spiropentadiene
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Pentadienyl
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Diisobutene
Organic compounds with the formula (CH3)2C6H4
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Xylene
Hydrocarbon compound containing one or more C=C bonds
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Alkene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
O-Xylene
Chemical compound
the product when gold(III) acetate is sonicated with cyclo-octasulfur in decalin. Hiroaki Sakurai; Kenji Koga; Yasuo Iizuka; Masato Kiuchi (2013). "Colorless
Gold(III)_acetate
Chemical compound
Sclareol is a fragrant chemical compound found in Salvia sclarea, from which it derives its name. It is classified as a bicyclic diterpene alcohol having
Sclareol
Covalent compound that contains two double bonds
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Diene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Anthracene
Molecule with a ring of bonded atoms
compound, with circles showing delocalization of π-electrons (aromatic). Decalin (decahydronaphthalene), the fully saturated derivative of naphthalene,
Cyclic_compound
Petrochemical process to break down saturated hydrocarbons in smaller molecules
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Steam_cracking
System for describing hydrocarbon compounds with multiple rings
Numbered skeletal formula of bicyclo[4.4.0]decane or Decalin. The grey numbers represent numbering according to the von Baeyer nomenclature.
Von_Baeyer_nomenclature
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Cymene
Chemical reaction
tyrosine. A synthesis of reserpine uses a Diels–Alder reaction to set the cis-decalin framework of the D and E rings. In another synthesis of reserpine, the
Diels–Alder_reaction
Type of saturated hydrocarbon compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Alkane
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Butadiene
Chemical compound
isopropyl group at position C-13 and a conjugated diene system within its decalin core, distinguishing it from the isolated double bond arrangement in abietic
Neoabietic_acid
Reaction in organic chemistry
system. This reaction can gives rise to various natural derivatives of decalin. Because the two reacting groups are already attached, two basic modes
Intramolecular Diels–Alder cycloaddition
Intramolecular_Diels–Alder_cycloaddition
Chemical compound
PMMA for example in confocal microscopy of colloids. A mixture of cis-decalin and CXB can simultaneously match optical index and density of PMMA. Due
Bromocyclohexane
Hydrocarbon compound made of a 5-carbon chain with two single and two double bonds
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Pentadiene
Index of articles associated with the same name
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
C4-Benzenes
Organic compounds with the empirical formula CH3C6H4CH2CH3
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Ethyltoluene
Polyketide
associated with PKS biosynthetic pathways (See Figure 1). Formation of the decalin ring is part of the PKS pathway and not a post-tailoring event. This occurs
Anthracimycin
Polycyclic aromatic hydrocarbon composed of three fused benzene rings
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Phenanthrene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Methylcyclopropane
Hydrocarbon compound containing a non-aromatic ring with a C=C bond
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Cycloalkene
Aromatic hydrocarbon
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Toluene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
2-Methylhexane
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Cyclopropyne
Oxidisation reaction
major product. Another example arises from the Étard reaction of trans-decalin which results in a mixture of trans-9-decalol, spiro [4.5]decan-6-one,
Étard_reaction
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Methylcyclobutane
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
1,7-Octadiene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
2,2,4-Trimethylpentane
Pericyclic chemical reaction
compound, proceeds 1,500 times faster in polar DMSO than in non-polar decalin. On the other hand, a close analog of this reaction, N-cyclohexenyl pyrrolidine
1,3-Dipolar_cycloaddition
Hydrocarbon compound; precursor to styrene and polystyrene
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Ethylbenzene
Saturated alicyclic hydrocarbon
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Cycloalkane
Chemical compound
(IMDA) to form its trans-decalin motif. 1,3-bisphosphoglycerate is converted to glyceryl S-ACP and condenses onto the decalin-bearing polyketide intermediate
Maklamicin
Class of chemical compounds
anions include hexaselenohypodiphosphate [P2Se6]4− and [P6Se12]4− with decalin structure and [P4Se2]2− with dicyclobutane structure. Selenophosphates
Selenophosphate
Species of fungus
"Antisense-Guided Isolation and Structure Elucidation of Pannomycin, a Substituted cis-Decalin from Geomyces pannorum". Journal of Natural Products. 72 (1): 59–62. Bibcode:2009JNAtP
Geomyces_pannorum
Unsaturated hydrocarbon compound (H2C=C(CH3)2)
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Isobutylene
Drug used to expel parasitic worms by paralyzing them
(+)-costunolide is reduced before the second ring closure. The bicyclic decalin ring system is formed via the eudesmyl cation followed by hydroxylation
Santonin
Chemical compound
as the product when auric acetate is sonicated with cyclo-octasulfur in decalin. Auric sulfide is claimed to react with nitric acid as well sodium cyanide
Gold(III)_sulfide
Group of chemical compounds
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Tetramethylbenzene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Mesitylene
Methods of storing hydrogen for later use
Cycloalkanes reported as LOHC include cyclohexane, methyl-cyclohexane and decalin. The dehydrogenation of cycloalkanes is highly endothermic (63-69 kJ/mol
Hydrogen_storage
Chemical compound
Nootkatone is an organic compound, a sesquiterpenoid, which means that it is a C15 derivative that also contains an oxygen-containing functional group
Nootkatone
Chemical compound
Caleicine is a unique sesquiterpene compound found exclusively in Calea ternifolia, a Mexican flowering plant known for its potential psychoactive properties
Caleicine
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Cyclohexyne
Hydrocarbon compound (C22H14) made of 5 fused benzene rings
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Pentacene
Family of organic compounds
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Alkylbenzene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Pyrene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
4-Ethyltoluene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
4-Vinyltoluene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
P-Cymene
Group of isomeric chemical compounds
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Trimethylbenzene
Chemical compound
Capsidiol is a terpenoid compound that accumulates in tobacco Nicotiana tabacum and chili pepper Capsicum annuum in response to fungal infection. Capsidiol
Capsidiol
Material which glows when excited by ionizing radiation
are toluene, xylene, benzene, phenylcyclohexane, triethylbenzene, and decalin. Liquid scintillators are easily loaded with other additives such as wavelength
Scintillator
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
1,5-Hexadiene
Chemical compound
Solubility soluble in chloroform, ethanol, acetone, ether, benzene, toluene, decalin, tetralin Magnetic susceptibility (χ) −1.26×10−4 cm3/mol Hazards GHS labelling:
Borneol
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Prismane
Mathematical element in composite engineering
tension. The most popular liquid currently in use is perfluoro- 1 - methyl decalin. Derek Hull. (1981).An Introduction to Composite Materials. Cambridge University
Fiber_volume_ratio
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Trans-Propenylbenzene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Spiropentane
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Housane
Chemical compound
Valencene is a sesquiterpene that is an aroma component of citrus fruit and citrus-derived odorants. It is obtained inexpensively from Valencia oranges
Valencene
Hydrocarbon compound containing one or more C≡C bonds
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Alkyne
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
N-Propylbenzene
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Cyclobutyne
Chemical compound
Bicycloalkanes Housane (bicyclo[2.1.0]pentane) Norbornane (bicyclo[2.2.1]heptane) Decalin (bicyclo[4.4.0]decane) Polycycloalkanes Adamantane Diamondoid Perhydrophenanthrene
Durene
DECALIN
DECALIN
DECALIN
DECALIN
Boy/Male
Muslim
Science
Girl/Female
American, British, English
Valiant Fighter; Brave Warrior; Nickname
Girl/Female
African, American, Australian, British, Chinese, Christian, English, French, German, Greek, Latin
Pure; Glowing; Form of Candace; Candy; Sweet; Prince of Servants
Girl/Female
Biblical
Revolution of inquiry.
Boy/Male
Muslim/Islamic
Person who keeps away from sins
Girl/Female
Hindu
Intelligent, Lord Krishna
Girl/Female
Sikh
Friendly king
Boy/Male
Hindu, Indian, Rajasthani, Traditional
Brave Lord; Similar to Virendra
Surname or Lastname
English (Yorkshire)
English (Yorkshire) : variant spelling of Woodmansee.
Girl/Female
Hindu
Full Moon, The person with knowledge as the Moon
DECALIN
DECALIN
DECALIN
DECALIN
DECALIN