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Details

Stereochemistry ACHIRAL
Molecular Formula C5H6OS
Molecular Weight 114.166
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of FURFURYL MERCAPTAN

SMILES

SCC1=CC=CO1

InChI

InChIKey=ZFFTZDQKIXPDAF-UHFFFAOYSA-N
InChI=1S/C5H6OS/c7-4-5-2-1-3-6-5/h1-3,7H,4H2

HIDE SMILES / InChI

Molecular Formula C5H6OS
Molecular Weight 114.166
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
A SABATH Methyltransferase from the moss Physcomitrella patens catalyzes S-methylation of thiols and has a role in detoxification.
2012-09
Synthesis and odor evaluation of five new sulfur-containing ester flavor compounds from 4-ethyloctanoic acid.
2010-07-29
μ(4)-Sulfido-bis-{(μ-2-furyl-methane-thiol-ato)bis-[tricarbonyl-iron](Fe-Fe)}.
2010-06-18
Molecular gastronomy: a new emerging scientific discipline.
2010-04-14
Reactivity of volatile thiols with polyphenols in a wine-model medium: impact of oxygen, iron, and sulfur dioxide.
2010-02-15
Odor detection of mixtures of homologous carboxylic acids and coffee aroma compounds by humans.
2009-11-11
Quantification and odor contribution of 2-furanmethanethiol in different types of fermented soybean paste miso.
2009-03-25
Optimization of a procedure for the selective isolation of some powerful aroma thiols. Development and validation of a quantitative method for their determination in wine.
2007-03-02
Influence of sulfur amino acids on the volatile and nonvolatile components of cooked salmon (Salmo salar).
2007-02-21
Automated analysis of 2-methyl-3-furanthiol and 3-mercaptohexyl acetate at ng L(-1) level by headspace solid-phase microextracion with on-fibre derivatisation and gas chromatography-negative chemical ionization mass spectrometric determination.
2006-07-14
A novel method for quantification of 2-methyl-3-furanthiol and 2-furanmethanethiol in wines made from Vitis vinifera grape varieties.
2006-01-11
Volatile constituents of glutathione--ribose model system and its antioxidant activity.
2003
Characterization of the aroma of a meatlike process flavoring from soybean-based enzyme-hydrolyzed vegetable protein.
2002-05-08
Formation of furfurylthiol exhibiting a strong coffee aroma during oak barrel fermentation from furfural released by toasted staves.
2001-10
Effect of pH and temperature on the formation of volatile compounds in cysteine/reducing sugar/starch mixtures during extrusion cooking.
2001-04
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:40:08 GMT 2025
Edited
by admin
on Mon Mar 31 18:40:08 GMT 2025
Record UNII
29W096TCPG
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FEMA NO. 2493
Preferred Name English
FURFURYL MERCAPTAN
FCC   FHFI  
Systematic Name English
2-FURANMETHANETHIOL
Systematic Name English
FURFURYL MERCAPTAN [FHFI]
Common Name English
2-FURYLMETHANETHIOL
Systematic Name English
FURFURYL MERCAPTAN [FCC]
Common Name English
NSC-41142
Code English
Classification Tree Code System Code
JECFA EVALUATION FURFURYL MERCAPTAN
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
Code System Code Type Description
WIKIPEDIA
Furfuryl mercaptan
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-628-2
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY
FDA UNII
29W096TCPG
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY
CAS
98-02-2
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY
PUBCHEM
7363
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID7052654
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY
NSC
41142
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY
JECFA MONOGRAPH
1004
Created by admin on Mon Mar 31 18:40:08 GMT 2025 , Edited by admin on Mon Mar 31 18:40:08 GMT 2025
PRIMARY