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Details

Stereochemistry ABSOLUTE
Molecular Formula C12H18O2
Molecular Weight 194.2701
Optical Activity ( + )
Defined Stereocenters 3 / 3
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PINOCARVYL ACETATE, TRANS-(+)-

SMILES

CC(=O)O[C@H]1C[C@H]2C[C@@H](C1=C)C2(C)C

InChI

InChIKey=UDBAGFUFASPUFS-VWYCJHECSA-N
InChI=1S/C12H18O2/c1-7-10-5-9(12(10,3)4)6-11(7)14-8(2)13/h9-11H,1,5-6H2,2-4H3/t9-,10+,11+/m1/s1

HIDE SMILES / InChI

Molecular Formula C12H18O2
Molecular Weight 194.2701
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 Sat Dec 16 15:15:07 GMT 2023
Edited
by admin
on Sat Dec 16 15:15:07 GMT 2023
Record UNII
3ZVF5VC3C3
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PINOCARVYL ACETATE, TRANS-(+)-
Common Name English
(+)-TRANS-PINOCARVOL ACETATE
Common Name English
FEMA NO. 4807, TRANS-(+)-
Code English
BICYCLO(3.1.1)HEPTAN-3-OL, 6,6-DIMETHYL-2-METHYLENE-, 3-ACETATE, (1R,3S,5R)-
Systematic Name English
2(10)-PINEN-3-OL, ACETATE, (1R,3S,5R)-
Common Name English
BICYCLO(3.1.1)HEPTAN-3-OL, 6,6-DIMETHYL-2-METHYLENE-, ACETATE, (1R-(1.ALPHA.,3.ALPHA.,5.ALPHA.))-
Common Name English
(+)-TRANS-PINOCARVYL ACETATE
Common Name English
Code System Code Type Description
CAS
33045-02-2
Created by admin on Sat Dec 16 15:15:08 GMT 2023 , Edited by admin on Sat Dec 16 15:15:08 GMT 2023
PRIMARY
EPA CompTox
DTXSID501142175
Created by admin on Sat Dec 16 15:15:08 GMT 2023 , Edited by admin on Sat Dec 16 15:15:08 GMT 2023
PRIMARY
FDA UNII
3ZVF5VC3C3
Created by admin on Sat Dec 16 15:15:08 GMT 2023 , Edited by admin on Sat Dec 16 15:15:08 GMT 2023
PRIMARY
PUBCHEM
6427491
Created by admin on Sat Dec 16 15:15:08 GMT 2023 , Edited by admin on Sat Dec 16 15:15:08 GMT 2023
PRIMARY
ECHA (EC/EINECS)
251-357-6
Created by admin on Sat Dec 16 15:15:08 GMT 2023 , Edited by admin on Sat Dec 16 15:15:08 GMT 2023
PRIMARY
Related Record Type Details
DIASTEREOISOMER -> DIASTEREOISOMER