Description

(1Alpha,2Beta,5Alpha)-6,6-Dimethylbicyclo[3.1.1]Heptane-2-Methanol is a high-purity, synthetically derived bicyclic monoterpenoid alcohol of significant interest in advanced organic synthesis. This compound matters as a versatile chiral building block and intermediate, prized for its rigid, three-dimensional structure which is instrumental in constructing complex molecular architectures. It is needed by research and development teams in the pharmaceutical, agrochemical, and fragrance industries for applications ranging from asymmetric catalysis to the synthesis of novel active ingredients.

Application

• Pharmaceutical Intermediate: Serves as a key chiral precursor in the synthesis of novel therapeutic agents and active pharmaceutical ingredients (APIs).
• Agrochemical Synthesis: Used in the research and development of new pesticides and herbicides, leveraging its unique steric properties.
• Fragrance & Flavor Chemistry: Acts as a building block for creating novel, complex odorants and flavor compounds with unique olfactory profiles.
• Asymmetric Catalysis: Employed as a ligand or a core structure in the design of chiral catalysts for enantioselective reactions.
• Material Science Research: Investigated as a monomer or additive for producing specialized polymers with tailored physical properties.
• Organic Synthesis Building Block: Provides a rigid, functionalized core for constructing complex natural product analogs and other specialty chemicals.

Basic Information

Product Name	(1Alpha,2Beta,5Alpha)-6,6-Dimethylbicyclo[3.1.1]Heptane-2-Methanol
CAS No.	15358-92-6
Molecular Formula	C10H18O
Molecular Weight	154.25 g/mol
Synonyms	(-)-Myrtenol; (1S,2R,5S)-Myrtenol; (1S,2R,5S)-6,6-Dimethylbicyclo[3.1.1]hept-2-ene-2-methanol; (1S,2R,5S)-2-Hydroxymethyl-6,6-dimethylbicyclo[3.1.1]hept-2-ene; L-Myrtenol; (1S,5S)-6,6-Dimethyl-2-methylene-bicyclo[3.1.1]heptan-3-ol (tautomer); Myrtenol (enantiomer)
EINECS	Contact for details

Quality Control

Our (1Alpha,2Beta,5Alpha)-6,6-Dimethylbicyclo[3.1.1]Heptane-2-Methanol is produced under strict quality management systems. Every batch undergoes rigorous analytical testing, including chiral purity assessment, to ensure it meets the high standards required for research and industrial synthesis. Certificates of Analysis (COA) with detailed specifications for identity, purity, and enantiomeric excess are available upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at controlled room temperature (15-25°C). Keep away from strong oxidizing agents.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to reference spectrum
Assay (GC)	≥ 97.0%
Enantiomeric Purity (Chiral GC/HPLC)	≥ 98.0% ee
Specific Rotation [α]	Contact for details
Water Content (KF)	≤ 0.5%

Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.