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Details

Stereochemistry RACEMIC
Molecular Formula C7H10O2
Molecular Weight 126.1531
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-HYDROXY-4-METHYL-5-HEXENOIC ACID .GAMMA. LACTONE

SMILES

CC1(CCC(=O)O1)C=C

InChI

InChIKey=QESPSAHXYXIGBG-UHFFFAOYSA-N
InChI=1S/C7H10O2/c1-3-7(2)5-4-6(8)9-7/h3H,1,4-5H2,2H3

HIDE SMILES / InChI

Molecular Formula C7H10O2
Molecular Weight 126.1531
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 20:26:36 GMT 2025
Edited
by admin
on Mon Mar 31 20:26:36 GMT 2025
Record UNII
S2GF56OA97
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-HYDROXY-4-METHYL-5-HEXENOIC ACID .GAMMA. LACTONE
FHFI  
Common Name English
FEMA NO. 4051
Preferred Name English
4-HYDROXY-4-METHYL-5-HEXENOIC ACID .GAMMA. LACTONE [FHFI]
Common Name English
.GAMMA.-METHYL-.GAMMA.-VINYL-.GAMMA.-BUTYROLACTONE
Common Name English
4-METHYL-4-VINYLBUTYROLACTONE
Common Name English
5-ETHENYLDIHYDRO-5-METHYL-2(3H)-FURANONE
Systematic Name English
.GAMMA.-VINYL-.GAMMA.-VALEROLACTONE
Common Name English
2(3H)-FURANONE, 5-ETHENYLDIHYDRO-5-METHYL-
Systematic Name English
4-METHYL-4-VINYL-4-BUTANOLIDE
Common Name English
2(3H)-FURANONE, DIHYDRO-5-METHYL-5-VINYL-
Systematic Name English
LILAC LACTONE
Common Name English
2-VINYL-2-METHYLTETRAHYDROFURAN-5-ONE
Systematic Name English
4-METHYL-5-HEXEN-4-OLIDE
Common Name English
LILAC LACTONE, (±)-
Common Name English
5-HEXENOIC ACID, 4-HYDROXY-4-METHYL-, .GAMMA.-LACTONE
Common Name English
(±)-LILAC LACTONE
Common Name English
LAVENDER LACTONE
Common Name English
.GAMMA.-VINYL-GAMMA.-VALEROLACTONE
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
214-024-6
Created by admin on Mon Mar 31 20:26:36 GMT 2025 , Edited by admin on Mon Mar 31 20:26:36 GMT 2025
PRIMARY
JECFA MONOGRAPH
1148
Created by admin on Mon Mar 31 20:26:36 GMT 2025 , Edited by admin on Mon Mar 31 20:26:36 GMT 2025
PRIMARY
CAS
1073-11-6
Created by admin on Mon Mar 31 20:26:36 GMT 2025 , Edited by admin on Mon Mar 31 20:26:36 GMT 2025
PRIMARY
PUBCHEM
102550
Created by admin on Mon Mar 31 20:26:36 GMT 2025 , Edited by admin on Mon Mar 31 20:26:36 GMT 2025
PRIMARY
FDA UNII
S2GF56OA97
Created by admin on Mon Mar 31 20:26:36 GMT 2025 , Edited by admin on Mon Mar 31 20:26:36 GMT 2025
PRIMARY
EPA CompTox
DTXSID40862523
Created by admin on Mon Mar 31 20:26:36 GMT 2025 , Edited by admin on Mon Mar 31 20:26:36 GMT 2025
PRIMARY