68327-11-7 | (1R,2R)-2-Aminocyclopentanol, HCl

Packsize	Purity	Availability	Price	Discounted Price
1g	95%	in stock	$15.00	$10.00
5g	95%	in stock	$23.00	$17.00
10g	95%	in stock	$43.00	$31.00
25g	95%	in stock	$99.00	$69.00
50g	95%	in stock	$193.00	$135.00
100g	95%	in stock	$383.00	$268.00

Description

• Catalog Number: AB47162
• Chemical Name: (1R,2R)-2-Aminocyclopentanol, HCl
• CAS Number: 68327-11-7
• Molecular Formula: C5H12ClNO
• Molecular Weight: 137.6079
• MDL Number: MFCD09834692
• SMILES: O[C@@H]1CCC[C@H]1N.Cl

Computed Properties

• Complexity: 65.1
• Covalently-Bonded Unit Count: 2
• Defined Atom Stereocenter Count: 2
• Heavy Atom Count: 8
• Hydrogen Bond Acceptor Count: 2
• Hydrogen Bond Donor Count: 3

Upstream Synthesis Route

Trans-(1R,2R)-2-Aminocyclopentanol Hydrochloride is a versatile compound widely utilized in chemical synthesis due to its unique stereochemistry and functional group reactivity. When incorporated into organic reactions, this compound acts as a chiral building block, providing asymmetry and specificity to the overall process. In particular, it serves as a valuable intermediate in the synthesis of complex organic molecules, pharmaceuticals, and biologically active compounds.This compound's application as a chiral auxiliary in asymmetric synthesis is particularly noteworthy. By leveraging the stereochemical properties of trans-(1R,2R)-2-Aminocyclopentanol Hydrochloride, chemists can exert control over the chirality of synthesized molecules, enabling the production of enantiomerically pure compounds with high optical purity. This capability is crucial in the production of pharmaceuticals and agrochemicals, where the stereochemistry of a molecule directly impacts its biological activity.Furthermore, trans-(1R,2R)-2-Aminocyclopentanol Hydrochloride can participate in a variety of reactions such as asymmetric reductions, cycloadditions, and transformations involving amino alcohols, offering a broad range of synthetic opportunities. Its ability to facilitate the formation of stereocenters and stereoselective transformations makes it a valuable tool for chemists seeking to access complex molecular architectures with high levels of stereocontrol.In summary, the role of trans-(1R,2R)-2-Aminocyclopentanol Hydrochloride in chemical synthesis is indispensable for achieving precise stereochemical control and accessing diverse structural motifs in the synthesis of valuable compounds. Its versatility and efficiency in promoting asymmetric transformations make it a key component in modern synthetic chemistry strategies.