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Details

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

SHOW SMILES / InChI
Structure of Campholenic aldehyde, (±)-

SMILES

CC1=CCC(CC=O)C1(C)C

InChI

InChIKey=OGCGGWYLHSJRFY-UHFFFAOYSA-N
InChI=1S/C10H16O/c1-8-4-5-9(6-7-11)10(8,2)3/h4,7,9H,5-6H2,1-3H3

HIDE SMILES / InChI

Molecular Formula C10H16O
Molecular Weight 152.2334
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 Sat Dec 16 18:41:00 GMT 2023
Edited
by admin
on Sat Dec 16 18:41:00 GMT 2023
Record UNII
3PT83BF2PD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Campholenic aldehyde, (±)-
Common Name English
NSC-58148
Code English
(±)-Campholenic aldehyde
Common Name English
3-Cyclopentene-1-acetaldehyde, 2,2,3-trimethyl-
Systematic Name English
2,2,3-Trimethyl-3-cyclopentene-1-acetaldehyde
Systematic Name English
NSC-96743
Systematic Name English
Campholenic aldehyde
Common Name English
2-(2,2,3-Trimethylcyclopent-3-enyl)acetaldehyde
Systematic Name English
Campholenealdehyde
Common Name English
α-Campholenic aldehyde
Common Name English
(±)-α-Campholenic aldehyde
Common Name English
2-(2,2,3-Trimethylcyclopent-3-en-1-yl)acetaldehyde
Systematic Name English
Code System Code Type Description
PUBCHEM
98497
Created by admin on Sat Dec 16 18:41:00 GMT 2023 , Edited by admin on Sat Dec 16 18:41:00 GMT 2023
PRIMARY
FDA UNII
3PT83BF2PD
Created by admin on Sat Dec 16 18:41:00 GMT 2023 , Edited by admin on Sat Dec 16 18:41:00 GMT 2023
PRIMARY
NSC
96743
Created by admin on Sat Dec 16 18:41:00 GMT 2023 , Edited by admin on Sat Dec 16 18:41:00 GMT 2023
PRIMARY
NSC
58148
Created by admin on Sat Dec 16 18:41:00 GMT 2023 , Edited by admin on Sat Dec 16 18:41:00 GMT 2023
PRIMARY
CAS
91819-58-8
Created by admin on Sat Dec 16 18:41:00 GMT 2023 , Edited by admin on Sat Dec 16 18:41:00 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE