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Details

Stereochemistry RACEMIC
Molecular Formula C10H20O
Molecular Weight 156.2652
Optical Activity ( + / - )
Defined Stereocenters 2 / 2
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2-TERT-BUTYLCYCLOHEXANOL, TRANS-

SMILES

CC(C)(C)[C@@H]1CCCC[C@H]1O

InChI

InChIKey=DLTWBMHADAJAAZ-RKDXNWHRSA-N
InChI=1S/C10H20O/c1-10(2,3)8-6-4-5-7-9(8)11/h8-9,11H,4-7H2,1-3H3/t8-,9-/m1/s1

HIDE SMILES / InChI

Molecular Formula C10H20O
Molecular Weight 156.2652
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 Sat Dec 16 11:18:16 GMT 2023
Edited
by admin
on Sat Dec 16 11:18:16 GMT 2023
Record UNII
9T74YJB0Y3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-TERT-BUTYLCYCLOHEXANOL, TRANS-
Systematic Name English
REL-(1R*,2S*)-2-TERT-BUTYL-1-CYCLOHEXANOL
Systematic Name English
TRANS-2-TERT-BUTYLCYCLOHEXAN-1-OL
Systematic Name English
TRANS-2-TERT-BUTYLCYCLOHEXANOL
Systematic Name English
CYCLOHEXANOL, 2-TERT-BUTYL-, TRANS-
Systematic Name English
NSC-17482
Code English
CYCLOHEXANOL, 2-(1,1-DIMETHYLETHYL)-, TRANS-
Systematic Name English
CYCLOHEXANOL, 2-(1,1-DIMETHYLETHYL)-, (1R,2S)-REL-
Systematic Name English
J422.743C
Code English
Code System Code Type Description
PUBCHEM
6995537
Created by admin on Sat Dec 16 11:18:16 GMT 2023 , Edited by admin on Sat Dec 16 11:18:16 GMT 2023
PRIMARY
EPA CompTox
DTXSID0052201
Created by admin on Sat Dec 16 11:18:16 GMT 2023 , Edited by admin on Sat Dec 16 11:18:16 GMT 2023
PRIMARY
CAS
5448-22-6
Created by admin on Sat Dec 16 11:18:16 GMT 2023 , Edited by admin on Sat Dec 16 11:18:16 GMT 2023
PRIMARY
NSC
17482
Created by admin on Sat Dec 16 11:18:16 GMT 2023 , Edited by admin on Sat Dec 16 11:18:16 GMT 2023
PRIMARY
ECHA (EC/EINECS)
226-670-6
Created by admin on Sat Dec 16 11:18:16 GMT 2023 , Edited by admin on Sat Dec 16 11:18:16 GMT 2023
PRIMARY
FDA UNII
9T74YJB0Y3
Created by admin on Sat Dec 16 11:18:16 GMT 2023 , Edited by admin on Sat Dec 16 11:18:16 GMT 2023
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE