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Details

Stereochemistry RACEMIC
Molecular Formula C10H16O
Molecular Weight 152.2334
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 1
Charge 0

SHOW SMILES / InChI
Structure of Marmelo oxide B, (±)-

SMILES

C[C@@H]1CO[C@H](C1)\C=C\C(C)=C

InChI

InChIKey=SULWOTZUSYCRIP-AWAZDUCLSA-N
InChI=1S/C10H16O/c1-8(2)4-5-10-6-9(3)7-11-10/h4-5,9-10H,1,6-7H2,2-3H3/b5-4+/t9-,10-/m0/s1

HIDE SMILES / InChI

Molecular Formula C10H16O
Molecular Weight 152.2334
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 1
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 22:58:09 GMT 2025
Edited
by admin
on Mon Mar 31 22:58:09 GMT 2025
Record UNII
JG2BE6Q3H6
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Furan, tetrahydro-4-methyl-2-(3-methyl-1,3-butadienyl)-, [2?(E),4?]-
Preferred Name English
Marmelo oxide B, (±)-
Common Name English
Furan, tetrahydro-4-methyl-2-(3-methyl-1,3-butadienyl)-, [2?(E),4?]-(±)-
Systematic Name English
Furan, tetrahydro-4-methyl-2-[(1E)-3-methyl-1,3-butadien-1-yl]-, (2R,4S)-rel-
Systematic Name English
rel-(2R,4S)-Tetrahydro-4-methyl-2-[(1E)-3-methyl-1,3-butadien-1-yl]furan
Systematic Name English
Code System Code Type Description
FDA UNII
JG2BE6Q3H6
Created by admin on Mon Mar 31 22:58:09 GMT 2025 , Edited by admin on Mon Mar 31 22:58:09 GMT 2025
PRIMARY
CAS
88623-82-9
Created by admin on Mon Mar 31 22:58:09 GMT 2025 , Edited by admin on Mon Mar 31 22:58:09 GMT 2025
SUPERSEDED
CAS
121009-48-1
Created by admin on Mon Mar 31 22:58:09 GMT 2025 , Edited by admin on Mon Mar 31 22:58:09 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE