Description

7,8-Diazatricyclo[4.2.2.02,5]Dec-7-Ene,(1R,2S,5R,6S)-Rel-(9Ci) is a high-value, stereochemically defined bicyclic diamine derivative, serving as a sophisticated chiral building block in advanced organic synthesis. Its rigid, three-dimensional scaffold and specific stereochemistry make it a critical intermediate for constructing complex molecular architectures with precise spatial orientation. This compound is essential for research and development chemists in the pharmaceutical and agrochemical industries, particularly for creating novel active ingredients, catalysts, and functional materials where chirality dictates biological activity and material properties.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the synthesis of novel drug candidates, especially in central nervous system (CNS) and antiviral research.
• Asymmetric Catalyst Ligand: Used to construct chiral ligands for transition metal catalysis, enabling enantioselective synthesis.
• Agrochemical Development: Serves as a building block for creating new, stereospecific pesticides and herbicides with improved efficacy and environmental profiles.
• Material Science Research: Employed in the development of chiral polymers, advanced resins, and specialty chemicals with unique optical or mechanical properties.
• Academic & R&D Laboratories: A valuable tool for methodological studies in organic chemistry and for exploring new synthetic pathways.
• Fine Chemical Synthesis: Used in the multi-step production of other high-value, complex specialty chemicals.

Basic Information

Product Name	7,8-Diazatricyclo[4.2.2.02,5]Dec-7-Ene,(1R,2S,5R,6S)-Rel-(9Ci)
CAS No.	645357-10-4
Molecular Formula	C8H10N2
Molecular Weight	134.18 g/mol
Synonyms	(1R,2S,5R,6S)-7,8-Diazatricyclo[4.2.2.02,5]dec-7-ene; rel-(1R,2S,5R,6S)-7,8-Diazatricyclo[4.2.2.02,5]dec-7-ene; Bicyclo[2.2.2]oct-5-ene-2,3-diamine derivative; 7,8-Diazabicyclo[4.2.2]dec-7-ene; (rel)-(1R,2S,5R,6S)-7,8-Diazatricyclo[4.2.2.02,5]dec-7-ene; 645357-10-4; SCHEMBL21845427
EINECS	Contact for details

Quality Control

Our production of this advanced intermediate adheres to strict quality management protocols to ensure batch-to-batch consistency and high purity. Each lot is characterized using advanced analytical techniques including HPLC, GC, NMR, and chiral analysis to confirm identity, purity, and enantiomeric excess. A comprehensive Certificate of Analysis (COA) detailing all specifications is provided with every shipment. We support development and scale-up projects with custom synthesis and purity grades upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, well-ventilated area at a controlled room temperature (15-25°C). The container should be kept tightly sealed in a dry environment to minimize exposure to moisture and air.

Specification

Item	Specification
Appearance	White to off-white solid
Identification (IR)	Conforms to structure
Purity (HPLC)	≥ 97.0%
Chiral Purity (Chiral HPLC)	≥ 98.0% e.e.
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.