73657-24-6

Basic information

• Product Name: (1R,2S)-(+)-BORNYLAMINE HCL
• Synonyms: (1R,2S)-(+)-BORNYLAMINE HCL ;(1R,2S)-1,7,7-Trimethyl-bicyclo[2.2.1]hept-2-ylamine hydrochloride;2S)-(+)-bornylaMineHCl;(1R,2S)-1,7,7-TriMethylbicyclo[2.2.1]heptan-2-aMine hydrochloride
• CAS NO: 73657-24-6
• Molecular Formula: C₁₀H₂₀N*Cl
• Molecular Weight: 189.7255
• Mol File: 73657-24-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 228.7 °C at 760 mmHg
• Flash Point: 92.1 °C
• Appearance: /
• Vapor Pressure: 0.0591mmHg at 25°C
• Storage Temp.: Sealed in dry,Room Temperature
• CAS DataBase Reference: (1R,2S)-(+)-BORNYLAMINE HCL(CAS DataBase Reference)
• NIST Chemistry Reference: (1R,2S)-(+)-BORNYLAMINE HCL(73657-24-6)
• EPA Substance Registry System: (1R,2S)-(+)-BORNYLAMINE HCL(73657-24-6)

Safety Data

• Hazardous Substances Data: 73657-24-6(Hazardous Substances Data)

Usage

General Description

(1R,2S)-(+)-BORNLYAMINE HCL, also known as bornylamine hydrochloride, is a chemical compound predominantly used in scientific research, oftentimes as an intermediate in the synthesis of more complex compounds or molecules. This colorless crystalline solid is known for its enantiomeric excess, meaning it contains more of one enantiomer than the other. (1R,2S)-(+)-BORNYLAMINE HCL exists in two forms, or enantiomers, which are mirror images of each other, and typically, one enantiomer is biologically active while the other is not. It's noteworthy for its role in stereospecific reactions—a type of reaction where the mechanism allows for the stereoselective formation of specific isomers. Despite its uses in laboratory environments, little information is available on its safety, toxicology or potential environmental impact, a common circumstance for such niche compounds.

InChI:InChI=1/C10H19N.ClH/c1-9(2)7-4-5-10(9,3)8(11)6-7;/h7-8H,4-6,11H2,1-3H3;1H/t7?,8-,10-;/m0./s1

Upstream product

• 2792-42-9 (R,R)-camphor oxime 

Relevant articles and documents

Synthesis of Optically Active Triazolinediones and Examination of Their Utility for Inducing Asymmetry in Diels-Alder Cycloaddition Reactions

(S)-(-)-α-Methylbenzylamine, dehydroabietylamine, and endo-bornylamine have been transformed into the optically pure triazolinediones via the respective isocyanates and urazoles.Their ability to discriminate between diastereomeric Diels-Alder transition states was determined in the case of two dienes, 2,4-p-menthadiene and α-phellandrene, which were prepared in racemic and optically active forms of known enantiomeric purity.Exhaustive cycloaddition to these dienes gave the needed pairs of adduct D reference points against which those obtained in the asymmetric induction studies could be compared.By this technique, simple plots of D vs. diastereomeric purity served to delineate not only the level of enantioselection but also the absolute configuration of the adducts.Due in part to their exceptionally high reactivity, the triazolinediones are not sufficiently selective to permit high levels of enantioselection.Rather, their usefulness lies in their ability to achieve nondestructive resolution of various nonobivously resolvable compounds.