METHYL SULFIDE

Details

Stereochemistry	ACHIRAL
Molecular Formula	C2H6S
Molecular Weight	62.134
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

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SMILES

CSC

InChI

InChIKey=QMMFVYPAHWMCMS-UHFFFAOYSA-N

InChI=1S/C2H6S/c1-3-2/h1-2H3

HIDE SMILES / InChI

Molecular Formula	C2H6S
Molecular Weight	62.134
Charge	0
Count	MOL RATIO 1 MOL RATIO (average)

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Show entries

Title	Date	PubMed
Biological effects of the metabolites of dimethyl sulfoxide.	1975 Jan 27	1055534
Hydroboration. 97. Synthesis of new exceptional chloroborane--Lewis base adducts for hydroboration. Dioxane--monochloroborane as a superior reagent for the selective hydroboration of terminal alkenes.	2001 Aug 10	11485456
Structural diversity in a family of copper(I) thioether complexes.	2001 Aug 13	11487333
Reactions of dimethylsulfoxide reductase in the presence of dimethyl sulfide and the structure of the dimethyl sulfide-modified enzyme.	2001 Aug 21	11502174
Active site heterogeneity in dimethyl sulfoxide reductase from Rhodobacter capsulatus revealed by Raman spectroscopy.	2001 Jan 16	11148038

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Substance Class	Chemical
Record UNII	QS3J7O7L3U
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

METHYL SULFIDE

Systematic Name

English

DIMETHYL SULFIDE [FCC]

Common Name

English

DIMETHYL THIOETHER

Systematic Name

English

DIMETHYL SULPHIDE

Systematic Name

English

DIMETHYL SULFIDE

Systematic Name

English

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Classification Tree

Code System

Code

Subpart F--Flavoring Agents and Related Substances

CFR

21 CFR 172.515

FUNCTIONAL CLASSIFICATION

JECFA EVALUATION

METHYL SULFIDE

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Code System

Code

Type

Description

EVMPD

SUB178195

PRIMARY

FDA UNII

QS3J7O7L3U

PRIMARY

CHEBI

17437

PRIMARY

MERCK INDEX

m4551

PRIMARY

Merck Index

HSDB

356

PRIMARY

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SMILES

InChI

Approval Year

PubMed

Patents