Description

Bicyclo[2.2.1]Heptan-2-Amine, 3-(2-Propenyl)-, (1S,3S,4R)-[Partial]- (9Ci) is a high-purity, stereochemically defined chiral amine building block, essential for advanced organic synthesis. Its unique norbornane-derived, allyl-substituted structure makes it a valuable precursor for constructing complex molecular architectures with precise three-dimensional control. This compound is primarily sought after by research and development chemists in the pharmaceutical and agrochemical industries for applications in asymmetric catalysis and the synthesis of novel active ingredients.

Application

• Pharmaceutical Intermediate: A key chiral synthon for the research and development of new active pharmaceutical ingredients (APIs), particularly in central nervous system (CNS) and antiviral drug candidates.
• Asymmetric Ligand Precursor: Used to synthesize novel chiral ligands and organocatalysts for enantioselective synthesis, improving yield and purity in fine chemical production.
• Agrochemical Research: Serves as a building block for developing new herbicides, fungicides, and insecticides with enhanced efficacy and selectivity.
• Material Science Monomer: Potential use in the synthesis of specialized polymers and resins with tailored thermal or mechanical properties.
• Academic & Industrial R&D: A critical reagent for methodological studies in organic chemistry, exploring new cycloaddition and functionalization reactions.

Basic Information

Product Name	Bicyclo[2.2.1]Heptan-2-Amine, 3-(2-Propenyl)-, (1S,3S,4R)-[Partial]- (9Ci)
CAS No.	186799-81-5
Molecular Formula	C10H17N
Molecular Weight	151.25 g/mol
Synonyms	(1S,3S,4R)-3-(2-Propenyl)bicyclo[2.2.1]heptan-2-amine; (1S,3S,4R)-3-Allyl-2-aminonorbornane; endo-3-Allyl-2-aminonorbornane; 3-Allylbicyclo[2.2.1]heptan-2-amine (stereoisomer); Chiral 3-Allylnorbornan-2-amine; Bicyclo[2.2.1]heptane-2-amine, 3-(2-propenyl)-, (1S,3S,4R)-; 186799-81-5
EINECS	Contact for details

Quality Control

Every batch of our chiral amine intermediates is produced and tested under strict quality management systems. We provide comprehensive analytical data to ensure identity, purity, and enantiomeric excess meet your specific research or production requirements. A Certificate of Analysis (COA) detailing results from chiral HPLC, GC, NMR, and optical rotation is available for each lot upon request.

Storage

Preserve in a tightly closed container, protected from light. Store in a cool, dry, and well-ventilated place at a controlled room temperature (15-25°C). This material is moisture-sensitive; keep the container tightly sealed under an inert atmosphere (e.g., nitrogen or argon) for long-term storage to prevent degradation.

Specification

Item	Specification
Appearance	Colorless to pale yellow liquid
Identification (IR)	Conforms to structure
Purity (GC)	≥ 97.0%
Enantiomeric Excess (Chiral HPLC)	≥ 99.0%
Water Content (KF)	≤ 0.5%

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