(1S,2R,3S,4S)-2,3-Dihydroxy-4-(hydroxymethyl)-1-aminocyclopentane hydrochloride, with the CAS number 77841-56-6, is a chemical compound characterized by its cyclic structure and multiple functional groups. This compound features a cyclopentane ring with two hydroxyl (-OH) groups and an amino (-NH2) group, contributing to its potential as a chiral molecule. The presence of these functional groups suggests that it may exhibit properties such as solubility in water and the ability to form hydrogen bonds, which can influence its reactivity and interaction with biological systems. The hydrochloride form indicates that the compound is a salt, which typically enhances its stability and solubility in aqueous solutions. This compound may be of interest in pharmaceutical applications due to its structural features, which could play a role in drug design and development, particularly in targeting specific biological pathways or receptors. Its stereochemistry, denoted by the (1S,2R,3S,4S) configuration, is crucial for its biological activity and interaction with other molecules.

(1S,2R,3S,4S)-2,3-DIHYDROXY-4-(HYDROXYMETHYL)-1-AMINOCYCLOPENTANE HYDROCHLORIDE

77841-56-6: (1S,2R,3S,4S)-2,3-Dihydroxy-4-(hydroxymethyl)-1-aminocyclopentane hydrochloride, with the CAS number 77841-56-6, is a chemical compound characterized by its cyclic structure and multiple functional groups. This compound features a cyclopentane ring with two hydroxyl (-OH) groups and an amino (-NH2) group, contributing to its potential as a chiral molecule. The presence of these functional groups suggests that it may exhibit properties such as solubility in water and the ability to form hydrogen bonds, which can influence its reactivity and interaction with biological systems. The hydrochloride form indicates that the compound is a salt, which typically enhances its stability and solubility in aqueous solutions. This compound may be of interest in pharmaceutical applications due to its structural features, which could play a role in drug design and development, particularly in targeting specific biological pathways or receptors. Its stereochemistry, denoted by the (1S,2R,3S,4S) configuration, is crucial for its biological activity and interaction with other molecules.

CAS 77841-56-6

(1S,2R,3S,4S)-2,3-DIHYDROXY-4-(HYDROXYMETHYL)-1-AMINOCYCLOPENTANE HYDROCHLORIDE

rac-(1R,2S,3R,5R)-3-Amino-5-(hydroxymethyl)cyclopentane-1,2-diol hydrochloride

Ref: 3D-CDA84156