C10H18O2
170.25 g/mol
Research ReagentWarning
(+)-Pinanediol
CAS18680-27-8EC606-096-6
Category
Research Reagent
Compound Class
Alcohol
Primary Use
Research Compound
(+)-Pinanediol is a chiral diol compound used as a building block in asymmetric synthesis. It features a rigid bicyclic structure derived from pinene, providing stereochemical control in synthetic transformations.
Chiral building block for asymmetric synthesisResearch reagent for stereoselective reactions
Content scope: Information here supports chemical identification and industrial supply, research, and manufacturing contexts. It is not a therapeutic claim, medical advice, or drug-use instructions.
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Referencesame scaffold
(1R,2R,3R,5S)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-amine
CAS69460-11-3
pharmaceutical intermediate
Safety Reference
Warning
H302Harmful if swallowed
H315Causes skin irritation
H319Causes serious eye irritation
H335May cause respiratory irritation
H412Harmful to aquatic life with long lasting effects
Customs Tariff Classification
The international HS code for (+)-Pinanediol (CAS 18680-27-8) is 2906.19.
HS code (international, 6-digit)
2906.19
EU CN code (8-digit)
2906 19 00
Classification per the EU customs inventory ECICS (2026-07 snapshot, HS 2022). National tariff lines and product form can affect the final classification.
Identifiers
IUPAC Name
(1S,2S,3R,5S)-2,6,6-trimethylbicyclo[3.1.1]heptane-2,3-diol
InChIKey
MOILFCKRQFQVFS-OORONAJNSA-N
SMILES
C[C@@]1([C@H]2C[C@H](C2(C)C)C[C@H]1O)O
Synonyms (14)
- (+)-2-Hydroxyisopinocampheol
- (+)-Pinanediol
- (1S,2S,3R,5S)-(+)-Pinanediol
- 2,3-cis/exo-pinanediol
- 2alpha,3alpha-Pinanediol
- Bortezomib Impurity 21
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