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Bicyclo[2.2.1]Heptan-2-Ol, 3-(Dimethylamino)-, (2-Exo,3-Endo)-(+)- (9Ci) CAS NO 117307-33-2
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CAS No.:117307-33-2
Grade:Pharmacy Grade
Content:99.9%
Brand:Customizable
Packaging:Customizable
Description
Bicyclo[2.2.1]Heptan-2-Ol, 3-(Dimethylamino)-, (2-Exo,3-Endo)-(+)- (9Ci) is a high-purity, chiral bicyclic amino alcohol building block of significant interest in advanced organic synthesis. Its unique stereochemistry and functional groups make it a valuable precursor for constructing complex molecular architectures, particularly in pharmaceutical research and fine chemical manufacturing. This compound is essential for chemists and R&D teams in the pharmaceutical, agrochemical, and specialty chemical industries seeking to develop novel active ingredients and chiral catalysts.
Application
- Pharmaceutical Intermediate: A key chiral synthon for the synthesis of novel drug candidates, particularly in central nervous system (CNS) and antiviral research.
- Asymmetric Catalyst Ligand: Serves as a precursor for chiral ligands used in asymmetric hydrogenation and other enantioselective transformations.
- Agrochemical Synthesis: Used in the research and development of advanced, stereospecific pesticides and herbicides.
- Fine Chemical Building Block: Employed in the multi-step synthesis of complex natural products, flavors, and fragrances.
- Academic & Industrial R&D: A valuable tool for methodological studies in organic chemistry and process development.
- Material Science Research: Potential monomer or modifier for creating polymers with specific stereochemical properties.
Basic Information
| Product Name | Bicyclo[2.2.1]Heptan-2-Ol, 3-(Dimethylamino)-, (2-Exo,3-Endo)-(+)- (9Ci) |
| CAS No. | 117307-33-2 |
| Molecular Formula | C9H17NO |
| Molecular Weight | 155.24 g/mol |
| Synonyms | (1R,2S,3R,4S)-3-(Dimethylamino)bicyclo[2.2.1]heptan-2-ol; (+)-3-(Dimethylamino)isoborneol; (+)-3-Dimethylaminonorborneol; (1R,2S,3R,4S)-3-(N,N-Dimethylamino)-2-norborneol; exo-2-Hydroxy-endo-3-dimethylaminonorbornane; 3-Dimethylaminonorbornan-2-ol; Amino alcohol catalyst precursor; Chiral norborneol derivative |
| EINECS | Contact for details |
Quality Control
Our production of this chiral intermediate adheres to strict quality management systems to ensure batch-to-batch consistency and high chemical purity. Every lot is characterized using advanced analytical techniques including HPLC, GC, and chiral analysis to confirm identity, enantiomeric excess, and impurity profiles. A comprehensive Certificate of Analysis (COA) detailing purity, assay, and specific test results is provided with each shipment to support your quality assurance and regulatory needs.
Storage
Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (typically 15-25°C). Due to its hygroscopic nature, the container must be kept tightly sealed after opening to minimize exposure to atmospheric moisture. Keep away from incompatible materials.
Specification
| Item | Specification |
|---|---|
| Appearance | White to off-white crystalline powder |
| Identification (IR) | Conforms to structure |
| Purity (HPLC) | ≥ 98.0% |
| Enantiomeric Excess (Chiral HPLC) | ≥ 99.0% |
| Water Content (KF) | ≤ 0.5% |
| Residue on Ignition | ≤ 0.1% |
Note: Specifications can be tailored. Please contact us for the detailed technical data sheet of a specific grade.
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Rigorous Quality Assurance
Each batch undergoes strict QC, accompanied by COA, MSDS, and full compliance with international standards.
Advanced R&D Expertise
Our in-house lab drives process innovation, new product development, and tailored synthesis solutions.






