U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ABSOLUTE
Molecular Formula C10H18O2
Molecular Weight 170.2487
Optical Activity UNSPECIFIED
Defined Stereocenters 4 / 4
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PINANEDIOL, (+)-

SMILES

CC1(C)[C@H]2C[C@@H]1[C@](C)(O)[C@H](O)C2

InChI

InChIKey=MOILFCKRQFQVFS-OORONAJNSA-N
InChI=1S/C10H18O2/c1-9(2)6-4-7(9)10(3,12)8(11)5-6/h6-8,11-12H,4-5H2,1-3H3/t6-,7-,8+,10-/m0/s1

HIDE SMILES / InChI

Description

PINANEDIOL, (+)- is a precursor to a chiral allyl boronate used in a preparation of chiral β-hydroxyallylsilanes.

Approval Year

Unknown
149124
Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct
PubMed

PubMed

TitleDatePubMed
(3aS,4S,6S,7aR)-Hexahydro-3a,5,5-trimethyl-2-phenyl-4,6-methano-1,3,2-benzodioxaborole.
2012-11-01
Total synthesis of (-)-microcarpalide, a novel microfilament disrupting metabolite.
2004-01-07
Patents

Patents

08680136
2
20050059636
2
20050107307
4
20050240047
1

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Name Type Language
PINANEDIOL, (+)-
Systematic Name English
2.ALPHA.,3.ALPHA.-PINANEDIOL
Preferred Name English
(1S,2S,3R,5S)-(+)-PINANE-2,3-DIOL
Systematic Name English
BICYCLO(3.1.1)HEPTANE-2,3-DIOL, 2,6,6-TRIMETHYL-, (1S-(1.ALPHA.,2.ALPHA.,3.ALPHA.,5.ALPHA.))-
Common Name English
BICYCLO(3.1.1)HEPTANE-2,3-DIOL, 2,6,6-TRIMETHYL-, (1S,2S,3R,5S)-
Systematic Name English
2,3-PINANEDIOL, (1S,2S,3R,5S)-(+)-
Systematic Name English
(+)-PINANEDIOL
Systematic Name English
(1S,2S,3R,5S)-(+)-2,6,6-TRIMETHYLBICYCLO(3.1.1)HEPTANE-2,3-DIOL
Systematic Name English
Code System Code Type Description
PUBCHEM
10219606
Created by admin on Mon Mar 31 21:01:54 GMT 2025 , Edited by admin on Mon Mar 31 21:01:54 GMT 2025
PRIMARY
CAS
18680-27-8
Created by admin on Mon Mar 31 21:01:54 GMT 2025 , Edited by admin on Mon Mar 31 21:01:54 GMT 2025
PRIMARY
FDA UNII
Y6ZCV4AVRA
Created by admin on Mon Mar 31 21:01:54 GMT 2025 , Edited by admin on Mon Mar 31 21:01:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID00171941
Created by admin on Mon Mar 31 21:01:54 GMT 2025 , Edited by admin on Mon Mar 31 21:01:54 GMT 2025
PRIMARY
SUBSTANCE RECORD
Structure of PINANEDIOL, (+)-
NIH
NCATS
PRIVACY NOTICE
ACCESSIBILITY
DISCLAIMER
HHS VULNERABILITY DISCLOSURE
For language access assistance, contact the NCATS Public Information Officer
National Center for Advancing Translational Sciences (NCATS),
6701 Democracy Boulevard, Bethesda MD 20892-4874 • 301-594-8966