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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
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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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