Description

Bicyclo[3.1.1]Heptane-2-Carboxaldehyde, 6,6-Dimethyl-, (1S,5S)-[Partial]- (9Ci) is a high-purity, chiral bicyclic aldehyde building block of significant interest in advanced organic synthesis. Its unique, rigid pinane-derived structure makes it a valuable precursor for creating complex molecules with specific stereochemistry. This compound is primarily sought after by research and development chemists in the pharmaceutical and agrochemical industries for the synthesis of novel active ingredients, fragrances, and specialty materials.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new drug candidates, particularly in creating molecules with defined three-dimensional architecture.
• Agrochemical Synthesis: Used in the development of novel pesticides and herbicides where the specific stereochemistry can influence biological activity.
• Fragrance and Flavor Chemistry: Serves as a building block for synthesizing terpene-based aroma chemicals and complex odorants.
• Asymmetric Catalysis Ligand Precursor: The aldehyde functionality and chiral centers can be elaborated to create novel ligands for asymmetric synthesis.
• Material Science Research: Employed in the synthesis of specialty polymers or organic frameworks with tailored properties.
• Academic and Industrial R&D: A valuable tool for methodological studies in organic chemistry and the exploration of new chemical spaces.

Basic Information

Product Name	Bicyclo[3.1.1]Heptane-2-Carboxaldehyde, 6,6-Dimethyl-, (1S,5S)-[Partial]- (9Ci)
CAS No.	185453-93-4
Molecular Formula	C10H16O
Molecular Weight	152.23 g/mol
Synonyms	(1S,5S)-6,6-Dimethylbicyclo[3.1.1]heptane-2-carboxaldehyde; (1S,5S)-2-Formyl-6,6-dimethylbicyclo[3.1.1]heptane; (+)-Myrtenal (specific enantiomer); (1S,5S)-Myrtenal; Pinane-2-carboxaldehyde derivative; Bicyclo[3.1.1]heptane-2-carboxaldehyde, 6,6-dimethyl-, (1S,5S)-; (1S,5S)-6,6-Dimethyl-2-norpinane-2-carboxaldehyde
EINECS	Contact for details

Quality Control

Our production of this chiral aldehyde adheres to stringent quality protocols to ensure batch-to-batch consistency and high chemical purity. Every lot is supported by a comprehensive Certificate of Analysis (COA) detailing purity, enantiomeric excess, and impurity profiles. We employ advanced analytical techniques including HPLC, GC, and chiral chromatography to meet the exacting standards required for research and process development applications.

Storage

Preserve in a tightly closed container, protected from light. Store under an inert atmosphere (e.g., nitrogen or argon) in a cool, dry place at 2-8°C for long-term stability. This compound is easily oxidized and light-sensitive; prolonged exposure to air, light, or elevated temperatures should be avoided to maintain purity.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (GC/HPLC)	≥ 97.0%
Enantiomeric Excess (Chiral HPLC)	≥ 98.0% ee
Water Content (KF)	≤ 0.5%

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