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Details

Stereochemistry RACEMIC
Molecular Formula C6H12O2
Molecular Weight 116.1583
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,2-CYCLOHEXANEDIOL, TRANS-

SMILES

O[C@@H]1CCCC[C@H]1O

InChI

InChIKey=PFURGBBHAOXLIO-PHDIDXHHSA-N
InChI=1S/C6H12O2/c7-5-3-1-2-4-6(5)8/h5-8H,1-4H2/t5-,6-/m1/s1

HIDE SMILES / InChI

Molecular Formula C6H12O2
Molecular Weight 116.1583
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 2 / 2
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Fri Dec 15 19:15:07 GMT 2023
Edited
by admin
on Fri Dec 15 19:15:07 GMT 2023
Record UNII
89G7G95Z1Y
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,2-CYCLOHEXANEDIOL, TRANS-
Systematic Name English
(±)-TRANS-1,2-CYCLOHEXANEDIOL
Systematic Name English
1,2-CYCLOHEXANEDIOL, (1R,2R)-REL-
Common Name English
J237.203G
Code English
NSC-150568
Code English
TRANS-CYCLOHEXANE-1,2-DIOL
Systematic Name English
TRANS-1,2-CYCLOHEXANEDIOL
Systematic Name English
TRANS-2-HYDROXYCYCLOHEXANOL
Systematic Name English
NSC-34836
Code English
TRANS-1,2-DIHYDROXYCYCLOHEXANE
Systematic Name English
Code System Code Type Description
NSC
34836
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
PUBCHEM
92886
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
ECHA (EC/EINECS)
215-956-6
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
CHEBI
16931
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
CAS
1460-57-7
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
EPA CompTox
DTXSID7075347
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
FDA UNII
89G7G95Z1Y
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
NSC
150568
Created by admin on Fri Dec 15 19:15:07 GMT 2023 , Edited by admin on Fri Dec 15 19:15:07 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE