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Chemical compound
In chemistry, dioxirane (systematically named dioxacyclopropane, also known as methylene peroxide or peroxymethane) is an organic compound with formula
Dioxirane
Chemical reaction
proceed via a dioxirane intermediate, generated when the oxone peroxidizes the catalyst ketone. (The oxone sulfate group facilitates dioxirane formation by
Shi_epoxidation
Oxidation with dioxiranes refers to the introduction of oxygen into organic substrates using dioxiranes. Dioxiranes are well known for epoxidations (synthesis
Oxidation_with_dioxiranes
Chemical compound
(DMDO) is the organic compound with the formula (CH3)2CO2. It is the dioxirane derived from acetone and can be viewed as the monomer of acetone peroxide
Dimethyldioxirane
Chemical compound
symmetry point groups Cs, D3h, and C2v. The C2v state, consisting of a dioxirane, has been shown to be the ground state of the molecule. Carbon trioxide
Carbon_trioxide
Chemical compound
the corresponding esters may be obtained. Oxone converts ketones to dioxiranes, which can be used for diverse oxidations in organic synthesis. and in
Oxone
Organic reaction
and Villiger suggested a dioxirane intermediate, while Georg Wittig and Gustav Pieper suggested a peroxide with no dioxirane formation. Carbon attack
Baeyer–Villiger_oxidation
Organic compounds of the form >C=O
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Ketone
Compound derived from an acid
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Ester
Chemical compound
Dimesityldioxirane is a substituted dioxirane with two mesityl groups attached to the dioxirane carbon. It is a colorless crystalline substance stable
Dimesityldioxirane
Organic compounds with a carbon-carbon-oxygen ring
without the intervention of metal catalysts. In specialized applications, dioxirane reagents (e.g. dimethyldioxirane) perform similarly, but are more explosive
Epoxide
Organic compound
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Urea
Chemical compounds and groups containing nitrogen with a lone pair (:N)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Amine
Chemical group (–OH)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Hydroxy_group
Organic compounds of the form RC(=O)NR′R″
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Amide
Chemical compound
an organic chemical consisting of a methyl group as substituent on a dioxirane ring. It is a highly unstable structure that has been proposed as part
Methyldioxirane
Molecule with one or more rings composed of different elements
Oxaziridine Oxazirine Nitrogen + Sulfur Thiaziridine Thiazirine 2 × Oxygen Dioxirane (highly unstable) - - - - - - 2 × Sulfur Dithiirane (highly unstable)
Heterocyclic_compound
Polyatomic ion (NO3, charge –1) found in explosives and fertilisers
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Nitrate
Organic compound with at least one hydroxyl (–OH) group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Alcohol_(chemistry)
Chemical group (>N–C(=O)–O–)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Carbamate
Chemical group (–C4H9) derived from butane
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Butyl_group
Any organic compound having a sulfanyl group (–SH)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Thiol
One of the lightest perfluoro compounds
arenes/AlCl3, respectively. Trifluoroacetone has been converted to the dioxirane using oxone. It serves as an oxidizing agent in Oppenauer oxidation. Trifluoracetone
Trifluoroacetone
Group of atoms giving a molecule characteristic properties
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Functional_group
Organic compound containing the functional group R–CH=O
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Aldehyde
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Reductone
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Ether
Chemical group (–N=C=O)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Isocyanate
Index of chemical compounds with the same molecular formula
formula CH2O2 (molar mass: 46.03 g/mol) may refer to: Dihydroxymethylidene Dioxirane, an unstable cyclic peroxide Formic acid, an organic acid Methylenedioxy
CH2O2
Chemical group (–CH2–CH=CH2)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Allyl_group
Type of saturated hydrocarbon compound
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Alkane
Functional group with the chemical structure R–S–S–R′
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Disulfide
Main-group allene analog
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
1-Phosphaallenes
Cyclic chemical group (–C6H5)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Phenyl_group
Organic compounds with the tautomeric structures RC(S)OH or RC(O)SH
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Thiocarboxylic_acid
Chemical species that accepts an electron pair from a nucleophile
catalyst, a ketone, is oxidized by stoichiometric oxone to the active dioxirane form before proceeding in the catalytic cycle. Oxaziridines such as chiral
Electrophile
Hydrocarbon compound (C6H6)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Benzene
Chemical compound
is a rare, stable member of the dioxirane family, known for a single oxygen-oxygen bond (O-O). Unlike most dioxiranes that decompose quickly, difluorodioxirane
Difluorodioxirane
Chemical compound
names 1,4-Bis(2,3-epoxypropoxy)butane (Tetramethylenebis(oxymethylene))dioxirane 1,4-Bis(2,3-epoxypropyloxy)butane 1,4-Bis(glycidyloxy)butane 1
1,4-Butanediol diglycidyl ether
1,4-Butanediol_diglycidyl_ether
Organic compounds of the form R–O–O–R′
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Organic_peroxides
Organic compound with the structure >C(O–)2
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Acetal
Chemical group (–CH2–CH3)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Ethyl_group
Chemical group, –C(=O)CH3
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Acetyl_group
Organic compound containing a –C(=O)OH group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Carboxylic_acid
Hydrocarbon compound containing one or more C=C bonds
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Alkene
Chemical compounds with the structure R–O–O–R'
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Peroxide
Chemical compound
SANDER, W. (1995-04-25). "ChemInform Abstract: Dimesityldioxirane (II): A Dioxirane Stable in the Solid State". ChemInform. 26 (17). Wiley. doi:10.1002/chin
Mesitaldehyde
Chemical group derived from alkanes (one hydrogen removed)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Alkyl_group
Organic compound with an –S– group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Organic_sulfide
Si–OH functional group in silicon chemistry
A wide range of oxidants have been employed including air, peracids, dioxiranes, and potassium permanganate (for hindered silanes). In the presence of
Silanol
Chemical group (–CH3) derived from methane
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Methyl_group
Organic compound containing an –NO2 group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Nitro_compound
Chemical group (–CH=CH2)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Vinyl_group
Class of organic compounds
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Chlorofluorocarbon
Organic compounds of the form R–O–N=O
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Alkyl_nitrite
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Arsonic acid (functional group)
Arsonic_acid_(functional_group)
Organic compound containing a sulfinyl group (>SO)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfoxide
Hydrocarbon compound (H2C=CH2)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Ethylene
Organic compounds with a diazenyl group (–N=N–)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Azo_compound
Chemical group (–N=C=S)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Isothiocyanate
Class of chemical compounds
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Hydroperoxide
Organosulfur compounds of the form R–SC(=O)–R′
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Thioester
Chemical group (–OCH3)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Methoxy_group
Chemical reaction which transfers an alkyl group between molecules
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Transalkylation
Chemical group (–CH2–C6H5)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Benzyl_group
Organosulfur compound of the form R–SOH
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfenic_acid
Chemical group (R–O)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Alkoxy_group
Functional group (C=O)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Carbonyl_group
Organic compound containing C–PO(OR)2 groups
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Phosphonate
Chemical reaction between silyl enol ethers and peroxyacids
substrate-controlled stereoselective Rubottom oxidation using dimethyl dioxirane(DMDO) as the oxidant and catalytic camphorsulfonic acid (CSA) to aid in
Rubottom_oxidation
rearrangement, reductive elimination reactions of dialkylmercury compounds, dioxirane dihydroxylations, and electrophilic fluorinations. Johnson, C.C.; Lippard
Radical_clock
Class of organic compounds
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Hydrazone
Class of chemical compounds
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Selenonic_acid
Chemical compound
Bozzelli JW (199). "Enthalpies of formation of cyclic alkyl peroxides: Dioxirane, 1,2-dioxetane, 1,2-dioxolane, and 1,2-dioxane". Chemical Physics Letters
1,2-Dioxolane
Chemical process
decomplexation involves oxidation of a low valent complex. Oxidants include air, dioxirane, ceric ammonium nitrate (CAN), and halogens. Oxidants are selected to
Decomplexation
Salt that is a metal-thioate/O-esters of dithiocarbonate
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Xanthate
Type of organosulfur compound
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfinylamine
19710-56-6 CH2O polyoxymethylene 9002-81-7 CH2OS sulfine 40100-16-1 CH2O2 dioxirane 157-26-6 CH2O2 formic acid 64-18-6 CH2O3 carbonic acid 463-79-6 CH2S thioformaldehyde
List of compounds with carbon number 1
List_of_compounds_with_carbon_number_1
Chemical compound containing carbon and at least one halogen
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Halocarbon
Group of chemical compounds derived from alkanes containing one or more halogens
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Haloalkane
Halogen compounds derived from methane
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Halomethane
Chemical group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfonanilide
Chemical compound with the group –N+≡C–
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Isocyanide
Organosulfur compound of the form >S(=O)2
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfone
Heterocyclic aromatic organic compound
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Pyridine
Method in organic chemistry
asymmetric epoxidation of trans- and trisubstituted olefins with chiral dioxiranes. Since that time, several different types of reactions have been developed
Organocatalysis
Class of chemical compounds
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Selenenic_acid
Organic compounds of the form >C=N–OH
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Oxime
Organic compounds with the structure R–S(=O)2–OH
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfonic_acid
Chemical compound (C5H5NO)
Angel (17 November 1997). "On the preparation of amine N-oxides by using dioxiranes". Tetrahedron. 53 (46): 15877–15888. Ochiai Eiji (1967). Aromatic Amine
Pyridine-N-oxide
Chemical group (–C3H7) derived from propane
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Propyl_group
Organosulfur compounds containing –S(=O)2–N< functional group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfonamide
Functional group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Methylenedioxy
Any chemical compound having two acyl groups bonded to the same oxygen atom
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Organic_acid_anhydride
Class of chemical compounds
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Imide
Any part of a molecule with the chemical formula –CH2–
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Methylene_bridge
Nitrogen-based molecule
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Nitrene
Chemical group (R–C=O)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Acyl_group
Organic compound with a –C≡N functional group
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Nitrile
Chemical group (>S(=O)2)
Acetal Alcohol Alkoxy Methoxy Ether Enol ether Epoxide Peroxy Hydroperoxy Dioxiranes Ethylenedioxy Methylenedioxy carbonyl Acyl Acetyl Acryloyl Benzoyl Aldehyde
Sulfonyl_group
DIOXIRANE
DIOXIRANE
DIOXIRANE
DIOXIRANE
Girl/Female
Arabic, Muslim
One who Praises a Lot
Girl/Female
Indian
Inference
Boy/Male
Sikh
The light of Love
Girl/Female
Arabic, Muslim
Gift
Boy/Male
Sikh
Lord Vishnu, Champion of truth
Boy/Male
Arabic
Above All
Girl/Female
Greek
Aphrodite.
Girl/Female
Indian
It Rains
Surname or Lastname
English
English : unexplained.
Male
Egyptian
, a high-priest of the god Amen Ra.
DIOXIRANE
DIOXIRANE
DIOXIRANE
DIOXIRANE
DIOXIRANE