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Details

Stereochemistry RACEMIC
Molecular Formula C7H12O
Molecular Weight 112.1696
Optical Activity ( + / - )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NORBORNEOL, EXO-

SMILES

O[C@H]1C[C@@H]2CC[C@H]1C2

InChI

InChIKey=ZQTYQMYDIHMKQB-VQVTYTSYSA-N
InChI=1S/C7H12O/c8-7-4-5-1-2-6(7)3-5/h5-8H,1-4H2/t5-,6+,7+/m1/s1

HIDE SMILES / InChI

Molecular Formula C7H12O
Molecular Weight 112.1696
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative analysis of chemical compositions and antimicrobial activities of essential oils from Abies holophylla and Abies koreana activities of essential oils from Abies holophylla and Abies koreana.
2009-04
Interpretation of conformational effects on 2-endo-norborneol by natural chemical shielding analysis.
2005-02-10
Inversion vs retention of configuration in gas-phase ammonium ion/alcohol reactions.
2002-02-22
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 21:48:23 GMT 2025
Edited
by admin
on Mon Mar 31 21:48:23 GMT 2025
Record UNII
V367XM6FYD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
J237.525G
Preferred Name English
NORBORNEOL, EXO-
Common Name English
(±)-EXO-NORBORNEOL
Common Name English
ISONORBORNEOL
Common Name English
EXO-2-HYDROXYBICYCLO(2.2.1)HEPTANE
Common Name English
2-NORBORNANOL, EXO-
Systematic Name English
D,L-EXO-NORBORNEOL
Common Name English
BICYCLO(2.2.1)HEPTAN-2-OL, (1R,2R,4S)-REL-
Systematic Name English
EXO-BICYCLO(2.2.1)HEPTAN-2-OL
Systematic Name English
NSC-167460
Code English
Code System Code Type Description
FDA UNII
V367XM6FYD
Created by admin on Mon Mar 31 21:48:23 GMT 2025 , Edited by admin on Mon Mar 31 21:48:23 GMT 2025
PRIMARY
WIKIPEDIA
exo-Norborneol
Created by admin on Mon Mar 31 21:48:23 GMT 2025 , Edited by admin on Mon Mar 31 21:48:23 GMT 2025
PRIMARY
ECHA (EC/EINECS)
207-845-6
Created by admin on Mon Mar 31 21:48:23 GMT 2025 , Edited by admin on Mon Mar 31 21:48:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID7022041
Created by admin on Mon Mar 31 21:48:23 GMT 2025 , Edited by admin on Mon Mar 31 21:48:23 GMT 2025
PRIMARY
NSC
167460
Created by admin on Mon Mar 31 21:48:23 GMT 2025 , Edited by admin on Mon Mar 31 21:48:23 GMT 2025
PRIMARY
CAS
497-37-0
Created by admin on Mon Mar 31 21:48:23 GMT 2025 , Edited by admin on Mon Mar 31 21:48:23 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE