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Details

Stereochemistry RACEMIC
Molecular Formula C10H16O2
Molecular Weight 168.2328
Optical Activity ( + / - )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-HYDROXYCAMPHOR, (1R-EXO-(±)-)-

SMILES

CC1(C)[C@@H]2CC[C@@]1(C)C(=O)[C@@H]2O

InChI

InChIKey=AXMKZEOEXSKFJI-XSSZXYGBSA-N
InChI=1S/C10H16O2/c1-9(2)6-4-5-10(9,3)8(12)7(6)11/h6-7,11H,4-5H2,1-3H3/t6-,7-,10+/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H16O2
Molecular Weight 168.2328
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 3 / 3
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Mon Mar 31 20:34:50 GMT 2025
Edited
by admin
on Mon Mar 31 20:34:50 GMT 2025
Record UNII
T50WQ65MDU
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-HYDROXYCAMPHOR, (1R-EXO-(±)-)-
Common Name English
2-BORNANONE, 3-HYDROXY-, EXO-
Preferred Name English
3-HYDROXYCAMPHOR [MI]
Common Name English
OXAPHOR
Brand Name English
BICYCLO(2.2.1)HEPTAN-2-ONE, 3-HYDROXY-1,7,7-TRIMETHYL-, (1R,3R,4S)-REL-
Systematic Name English
EXO-3-HYDROXY-2-BORNANONE
Common Name English
BICYCLO(2.2.1)HEPTAN-2-ONE, 3-HYDROXY-1,7,7-TRIMETHYL-, EXO-
Systematic Name English
Code System Code Type Description
CAS
22759-33-7
Created by admin on Mon Mar 31 20:34:50 GMT 2025 , Edited by admin on Mon Mar 31 20:34:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID70871204
Created by admin on Mon Mar 31 20:34:50 GMT 2025 , Edited by admin on Mon Mar 31 20:34:50 GMT 2025
PRIMARY
CAS
82264-38-8
Created by admin on Mon Mar 31 20:34:50 GMT 2025 , Edited by admin on Mon Mar 31 20:34:50 GMT 2025
SUPERSEDED
CAS
25127-00-8
Created by admin on Mon Mar 31 20:34:50 GMT 2025 , Edited by admin on Mon Mar 31 20:34:50 GMT 2025
SUPERSEDED
FDA UNII
T50WQ65MDU
Created by admin on Mon Mar 31 20:34:50 GMT 2025 , Edited by admin on Mon Mar 31 20:34:50 GMT 2025
PRIMARY
CAS
10373-81-6
Created by admin on Mon Mar 31 20:34:50 GMT 2025 , Edited by admin on Mon Mar 31 20:34:50 GMT 2025
NON-SPECIFIC STEREOCHEMISTRY
Related Record Type Details
ENANTIOMER -> RACEMATE