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Details

Stereochemistry ACHIRAL
Molecular Formula C3H8S
Molecular Weight 76.161
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of ETHYL METHYL SULFIDE

SMILES

CCSC

InChI

InChIKey=WXEHBUMAEPOYKP-UHFFFAOYSA-N
InChI=1S/C3H8S/c1-3-4-2/h3H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C3H8S
Molecular Weight 76.161
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Prediction of conformational changes by single mutation in the hepatitis B virus surface antigen (HBsAg) identified in HBsAg-negative blood donors.
2010-11-18
Polarizable empirical force field for sulfur-containing compounds based on the classical Drude oscillator model.
2010-09
A comparative approach linking molecular dynamics of altered peptide ligands and MHC with in vivo immune responses.
2010-07-19
Irradiation effects on meat flavor: A review.
2009-01
Environmental chamber study of the photochemical reaction of ethyl methyl sulfide and NO(x).
2009
Altered spin state equilibrium in the T309V mutant of cytochrome P450 2D6: a spectroscopic and computational study.
2007-06
Ab initio molecular dynamics of heme in cytochrome c.
2007-02-08
Mechanisms for the selective gas-phase fragmentation reactions of methionine side chain fixed charge sulfonium ion containing peptides.
2006-12
Tris(thioimidazolyl)borate-zinc-thiolate complexes for the modeling of biological thiolate alkylations.
2005-11-14
Binding of the general anesthetics chloroform and 2,2,2-trichloroethanol to the hydrophobic core of a four-alpha-helix bundle proteins.
2003-01
Oxidative degradation of dimethyl sulfoxide by Cryptococcus humicolus WU-2, a newly isolated yeast.
2003
3-Pyrroline containing arylacetamides: a novel series of remarkably selective kappa-agonists.
2002-09-02
Trace determination of volatile sulfur compounds by solid-phase microextraction and GC-MS.
2002-08
Synthesis of novel quaternary amino acids using molybdenum-catalyzed asymmetric allylic alkylation.
2002-06-26
Docking studies reveal a selective binding of D-penicillamine to the transactivator protein of human immunodeficiency virus type 1.
2002-04-10
Characterization of amino acid side chain losses in electron capture dissociation.
2002-03
Off-odor volatiles and pink color development in precooked, irradiated turkey breast during frozen storage.
2002-02
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:54:23 GMT 2025
Edited
by admin
on Mon Mar 31 19:54:23 GMT 2025
Record UNII
MR1GZS62TM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
ETHYL METHYL SULFIDE
Systematic Name English
METHYL ETHYL SULFIDE
FHFI  
Preferred Name English
SULFIDE, ETHYL METHYL
Systematic Name English
2-THIABUTANE
Systematic Name English
1-(METHYLTHIO)ETHANE
Systematic Name English
(METHYLTHIO)ETHANE
Systematic Name English
ETHYL METHYL THIOETHER
Systematic Name English
METHYL ETHYL SULFIDE [FHFI]
Common Name English
FEMA NO. 3860
Code English
ETHANE, (METHYLTHIO)-
Systematic Name English
Classification Tree Code System Code
JECFA EVALUATION METHYL ETHYL SULFIDE
Created by admin on Mon Mar 31 19:54:23 GMT 2025 , Edited by admin on Mon Mar 31 19:54:23 GMT 2025
Code System Code Type Description
CAS
624-89-5
Created by admin on Mon Mar 31 19:54:23 GMT 2025 , Edited by admin on Mon Mar 31 19:54:23 GMT 2025
PRIMARY
JECFA MONOGRAPH
533
Created by admin on Mon Mar 31 19:54:23 GMT 2025 , Edited by admin on Mon Mar 31 19:54:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID3060794
Created by admin on Mon Mar 31 19:54:23 GMT 2025 , Edited by admin on Mon Mar 31 19:54:23 GMT 2025
PRIMARY
PUBCHEM
12230
Created by admin on Mon Mar 31 19:54:23 GMT 2025 , Edited by admin on Mon Mar 31 19:54:23 GMT 2025
PRIMARY
FDA UNII
MR1GZS62TM
Created by admin on Mon Mar 31 19:54:23 GMT 2025 , Edited by admin on Mon Mar 31 19:54:23 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-868-4
Created by admin on Mon Mar 31 19:54:23 GMT 2025 , Edited by admin on Mon Mar 31 19:54:23 GMT 2025
PRIMARY