Description

Bicyclo[2.2.1]Heptane, 2-Bromo-, (1R,2S,4S)-Rel- (9Ci) is a high-purity, stereochemically defined brominated norbornane derivative that serves as a critical chiral building block in advanced organic synthesis. Its rigid bicyclic framework and specific bromine substitution make it an invaluable intermediate for constructing complex molecular architectures with precise stereochemical control. This compound is essential for researchers and process chemists in the pharmaceutical, agrochemical, and specialty materials industries, where it is used to develop novel active ingredients and functional molecules.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the synthesis of novel drug candidates, particularly in central nervous system (CNS) and antiviral research.
• Agrochemical Development: Used in creating advanced pesticides and herbicides with specific stereochemical activity.
• Ligand and Catalyst Synthesis: Serves as a precursor for chiral ligands and organocatalysts used in asymmetric synthesis.
• Material Science Research: Employed in the development of specialty polymers and advanced organic materials with unique properties.
• Academic & R&D: A valuable tool for methodological studies in organic chemistry and stereoselective transformations.
• Fine Chemical Production: Intermediate for the manufacture of complex fragrance and flavor molecules.

Basic Information

Item	Detail
Product Name	Bicyclo[2.2.1]Heptane, 2-Bromo-, (1R,2S,4S)-Rel- (9Ci)
CAS No.	13237-87-1
Molecular Formula	C7H11Br
Molecular Weight	175.07 g/mol
Synonyms	(1R,2S,4S)-2-Bromonorbornane; rel-(1R,2S,4S)-2-Bromobicyclo[2.2.1]heptane; 2-Bromo-exo-norbornane (stereospecific); Bicyclo[2.2.1]heptane, 2-bromo-, (1R,2S,4S)-rel-; 2-Bromonorbornane (endo/endo isomer); NSC 169102; Bromonorbornane derivative
EINECS	Contact for details

Quality Control

Every batch of our (1R,2S,4S)-2-Bromonorbornane is produced under strict quality management systems. We employ advanced analytical techniques, including chiral HPLC, GC, and NMR spectroscopy, to ensure high chemical and enantiomeric purity for demanding synthetic applications. Comprehensive Certificates of Analysis (COA) detailing identity, purity, and impurity profiles are provided with each shipment to guarantee reproducible performance and traceability in your processes.

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). Keep away from strong acids and incompatible organic solvents. For long-term storage, consider maintaining the material under an inert atmosphere to preserve stability.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (GC)	≥ 97.0%
Chiral Purity (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.