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Details

Stereochemistry RACEMIC
Molecular Formula C14H22O2S
Molecular Weight 254.388
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-((2-METHYL-3-FURYL)THIO)-5-NONANONE

SMILES

CCCCC(=O)C(CCC)SC1=C(C)OC=C1

InChI

InChIKey=PEYZZTQOVLTVHN-UHFFFAOYSA-N
InChI=1S/C14H22O2S/c1-4-6-8-12(15)14(7-5-2)17-13-9-10-16-11(13)3/h9-10,14H,4-8H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C14H22O2S
Molecular Weight 254.388
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:52:48 GMT 2025
Edited
by admin
on Mon Mar 31 19:52:48 GMT 2025
Record UNII
DQZ4Y02VLM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-((2-METHYL-3-FURYL)THIO)-5-NONANONE
FHFI  
Systematic Name English
FEMA NO. 3571
Preferred Name English
(±)-4-((2-METHYL-3-FURYL)THIO)-5-NONANONE
Systematic Name English
4-((2-METHYL-3-FURYL)THIO)-5-NONANONE, (±)-
Systematic Name English
1,3-DIPROPYLACETONYL 2-METHYL-3-FURYL SULFIDE
Systematic Name English
4-((2-METHYL-3-FURYL)THIO)-5-NONANONE [FHFI]
Common Name English
5-NONANONE, 4-((2-METHYL-3-FURANYL)THIO)-
Systematic Name English
Code System Code Type Description
CAS
61295-50-9
Created by admin on Mon Mar 31 19:52:48 GMT 2025 , Edited by admin on Mon Mar 31 19:52:48 GMT 2025
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EPA CompTox
DTXSID60866846
Created by admin on Mon Mar 31 19:52:48 GMT 2025 , Edited by admin on Mon Mar 31 19:52:48 GMT 2025
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PUBCHEM
62182
Created by admin on Mon Mar 31 19:52:48 GMT 2025 , Edited by admin on Mon Mar 31 19:52:48 GMT 2025
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JECFA MONOGRAPH
1019
Created by admin on Mon Mar 31 19:52:48 GMT 2025 , Edited by admin on Mon Mar 31 19:52:48 GMT 2025
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FDA UNII
DQZ4Y02VLM
Created by admin on Mon Mar 31 19:52:48 GMT 2025 , Edited by admin on Mon Mar 31 19:52:48 GMT 2025
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ECHA (EC/EINECS)
262-691-7
Created by admin on Mon Mar 31 19:52:48 GMT 2025 , Edited by admin on Mon Mar 31 19:52:48 GMT 2025
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