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Functional group
In organosulfur chemistry, thiosulfinate is a functional group consisting of the linkage R−S(O)−S−R (R refers to organic substituents). Thiolsulfinates
Thiosulfinate
Chemical compound
odor. It is a thioester of a sulfinic acid. It is also known as allyl thiosulfinate. Its biological activity can be attributed to both its antioxidant activity
Allicin
Functional group with the chemical structure R–S–S–R′
+ Cl2 → 2 ArSCl More unusually, oxidation of disulfides gives first thiosulfinates and then thiosulfonates: RSSR + [O] → RS(=O)SR RS(=O)SR + [O] → RS(=O)2SR
Disulfide
Chemical compound
well as oxidation with hydrogen peroxide or peracetic acid giving the thiosulfinate compound, methyl methanethiosulfinate (CH3S(O)SCH3). DMDS is used as
Dimethyl_disulfide
Genus of flowering plants
compounds serve as the precursors of several thiosulfinates such as S-(2-hydroxyethyl) 2-hydroxyethane)thiosulfinate, S-(2-hydroxylethyl) phenylmethanethiosulfinate
Petiveria
Iron (II) disulfide mineral
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Pyrite
Any organic compound having a sulfanyl group (–SH)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Thiol
Organic compounds of the form >C=O
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Ketone
Chemical group (–OH)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Hydroxy_group
Chemical group (–N=C=O)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Isocyanate
Chemical compounds with the structure R–O–O–R'
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Peroxide
Organic compounds made of alkyl/aryl groups bound to oxygen (R–O–R')
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Ether
Class of chemical compounds
sufinyl derivatives such as sulfinamides, sulfinates, sulfoxides, and thiosulfinates. Unlike the sulfur atom in sulfonyl halides and sulfenyl halides, the
Sulfinyl_halide
Organic compound
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Urea
Species of creeping annual plant
acid, propane sulfinic acid, 2-mercaptoaniline, S-propyl propane 1-thiosulfinate, and thioformaldehyde, an elusive and highly unstable compound never
Mimosa_pudica
Chemical compound (H2SO4)
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Sulfuric_acid
American organic chemist
compounds known as thiosulfinates. He also synthesized and reported on the chemical and biological properties of a series of thiosulfinates related to allicin
Chester_John_Cavallito
Chemical compound and greenhouse gas
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Sulfur_hexafluoride
Group of atoms giving a molecule characteristic properties
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Functional_group
Chemical compound
enantioselective oxidation of inexpensive di-tert-butyl disulfide to the thiosulfinate followed by disulfide bond cleavage by lithium amide. In the original
Tert-Butanesulfinamide
Species of flowering plant
lachrymatory agent (Z)-butanethial S-oxide, along with several 1-butenyl thiosulfinates have been detected in crushed plant material by mass spectrometry using
Allium_siculum
Hydrocarbon compound (H2C=CH2)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Ethylene
Reaction mechanism in organic chemistry
ester through a 6-membered cyclic transition state yields the alkene. Thiosulfinates can eliminate in the manner analogous to sulfoxides. Representative
Ei_mechanism
Corrosive liquid of excess sulfur trioxide in solution
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Oleum
Poisonous and flammable gas
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Hydrogen_sulfide
Hot or spicy flavor
to chemical substances. Substances such as piperine, capsaicin, and thiosulfinates can cause a burning or tingling sensation by inducing a trigeminal nerve
Pungency
Organic compounds of the form R–O–O–R′
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Organic_peroxides
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Ethylene_episulfoxide
Chemical group (–CH2–)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Methylene_group
Organic compounds of the form RC(=O)NR′R″
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Amide
Chemical compound of sulfur and oxygen
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Sulfur_dioxide
Chemical compound
mainly in Japan. These efforts led to the discovery of allicin (diallyl thiosulfinate) in garlic, which became a model for medicinal chemistry efforts to
Sulbutiamine
Functional group (C=O)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Carbonyl_group
Organic compound containing the functional group R–CH=O
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Aldehyde
Chemical group derived from alkanes (one hydrogen removed)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Alkyl_group
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Martin's_sulfurane
Organosulfur compound of the form R–SOH
which prevent the sulfenic acid from condensing with itself to form thiosulfinates, RS(O)SR, such as allicin from garlic. Through the use of X-ray crystallography
Sulfenic_acid
Chemical group, –C(=O)CH3
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Acetyl_group
Chemical group (>N–C(=O)–O–)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Carbamate
Chemical group
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Sulfonanilide
Organic compounds with the structure >C=S
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Thioketone
Lubricant additive
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Zinc_dithiophosphate
Compound derived from an acid
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Ester
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Reductone
Organic compound with a –C≡N functional group
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Nitrile
Organic compounds with a carbon-carbon-oxygen ring
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Epoxide
Chemical group (–C(=O)C6H5
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Benzoyl_group
Chemical group (–CH3) derived from methane
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Methyl_group
Group of chemical compounds derived from alkanes containing one or more halogens
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Haloalkane
Arsenic sulfide mineral
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Realgar
Heterocyclic aromatic organic compound
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Pyridine
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Potassium_sulfate
Organic compound containing a –C(=O)OH group
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Carboxylic_acid
Chemical group (–C4H9) derived from butane
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Butyl_group
Inorganic compound (SOCl2)
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Thionyl_chloride
Chemical derived from gypsum used in food and industry
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Calcium_sulfate
Class of chemical compounds
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Hydroperoxide
Chemical compounds and groups containing nitrogen with a lone pair (:N)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Amine
Chemical group (R–O)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Alkoxy_group
Chemical element with atomic number 16 (S)
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Sulfur
Chemical group (–CH2–CH3)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Ethyl_group
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Sulfur_trioxide
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Copper(II)_sulfate
Chemical compound
effect in a cellular model of Friedreich's ataxia. β-lipoic acid is a thiosulfinate of α-lipoic acid Aminolevulinic acid "Lipoic acid". PubChem, US National
Lipoic_acid
Cyclic chemical group (–C6H5)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Phenyl_group
Organic compounds with the structure R–S(=O)2–OH
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Sulfonic_acid
Any organic compound containing a C=C=C group
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Allene
Chemical group (–CH2–CH=CH2)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Allyl_group
Chemical group (R–C=O)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Acyl_group
Organic compound containing an –NO2 group
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Nitro_compound
Salt that is a metal-thioate/O-esters of dithiocarbonate
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Xanthate
Organosulfur compound of the form >S(=O)2
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Sulfone
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Gadolinium_oxysulfide
Sulfur-containing aromatic compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Thiophene
Organic compounds with a diazenyl group (–N=N–)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Azo_compound
Chemical compound
Spectrometry in Allium Chemistry. (Z)-Butanethial S-Oxide and 1-Butenyl Thiosulfinates and their S-(E)-1-Butenylcysteine S-Oxide Precursor from Allium siculum"
Syn-Propanethial-S-oxide
Class of organic compounds
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Hydrazone
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
3,4-Ethylenedioxythiophene
Organic compound with the structure >C(O–)2
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Acetal
Organosulfur compounds of the form R–SC(=O)–R′
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Thioester
Nitrogen-based molecule
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Nitrene
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Potassium_alum
Chemical compound
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Pentyl_group
Class of organic compounds
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Chlorofluorocarbon
Class of chemical compounds
organosulfur compounds containing the anion with the formula R−S−SO−3 Thiosulfinate a structurally analogous compound containing functional group in a lower
Thiosulfonate
Chemical mixture used as a pest control agent
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Lime_sulfur
Chemical group (–CH=CH2)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Vinyl_group
Any chemical compound having two acyl groups bonded to the same oxygen atom
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Organic_acid_anhydride
Organic compounds of the form >C=N–OH
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Oxime
Hydrocarbon compound (C6H6)
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Benzene
Polyatomic ion (NO3, charge –1) found in explosives and fertilisers
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Nitrate
Chemical compound with the group –N+≡C–
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Isocyanide
Organic compound with an –S– group
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Organic_sulfide
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Trisulfuryl_fluoride
Chemical compound
which is responsible for the aroma of fresh garlic. Allicin and other thiosulfinates in garlic are unstable and form a number of other compounds, such as
Alliin
Chemical compounds with a sulfur atom
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Sulfur_compounds
Class of chemical compounds
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Sulfite_ester
Hydrocarbon compound containing one or more C=C bonds
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Alkene
Chemical compound
Disulfide C32H66S2 Heterocycles Lipoic acid Trisulfide CH3SSSCH3 Thiosulfinate Allicin Sulfinic acid Hypotaurine Sulfone CFNO3S C2N2O4S Sulfonate Coenzyme
Disulfur_dichloride
Organic compounds with the tautomeric structures RC(S)OH or RC(O)SH
Thioether Sulfonium Thia-crown ether Persulfide Disulfide Sulfenic acid Thiosulfinate Sulfoxide Thiosulfonate Sulfinic acid Sulfone Sulfonic acid Thioketone
Thiocarboxylic_acid
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Variant spelling of Slavic Belobog, BIELOBOG means "white god."Â
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American, Australian, British, Chinese, Danish, English, French, German, Latin, Portuguese, Spanish, Swedish, Teutonic
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