122624-77-5

Basic information

• Product Name: (1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol
• Synonyms: (1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol;((1R,4S)-4-((2,5-Diamino-6-chloropyrimidin-4-yl)amino)cyclopent-2-en-1-yl)methanol
• CAS NO: 122624-77-5
• Molecular Formula: C10H14 Cl N5 O
• Molecular Weight: 255.7
• Product Categories: API
• Mol File: 122624-77-5.mol
• Article Data: 1

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: (1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol(122624-77-5)
• EPA Substance Registry System: (1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol(122624-77-5)

Safety Data

• Hazardous Substances Data: 122624-77-5(Hazardous Substances Data)

Usage

Description

(1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol is a complex organic compound characterized by a cyclopentene ring fused with a 2,5-diamino-6-chloropyrimidin-4-yl group and an amino group. Its stereochemistry is defined by the 1S,4R configuration, which dictates the spatial arrangement of its chiral centers. (1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol may hold promise for pharmaceutical applications due to the presence of an amino group and a chloropyrimidine moiety, both of which are prevalent in biologically active molecules.

Uses

Used in Pharmaceutical Industry:
(1S,4R)-4-(2',5'-diamino-6'-chloropyrimidin-4'-yl)amino>cyclopent-2-enylmethanol is used as a potential pharmaceutical agent for the development of new drugs. Its unique structure, featuring both an amino group and a chloropyrimidine moiety, positions it as a candidate for various therapeutic applications. The specific uses and efficacy of this compound in drug development would depend on further research and clinical trials to determine its safety, pharmacokinetics, and mechanism of action.

Upstream product

• 122624-75-3 (+/-)-cis-<4-<<2-amino-6-chloro-5-<(4-chlorophenyl)azo>-4-pyrimidinyl>amino>-2-cyclopentenyl>carbinol 
• 229177-39-3 1-amino-4-(hydroxymethyl)-2-cyclopentene 
• 61865-50-7 Acetic acid 4-acetylamino-cyclopent-2-enylmethyl ester 
• 122624-73-1 (+/-)-cis-<4-<(2-amino-6-chloro-4-pyrimidinyl)amino>-2-cyclopentenyl>carbinol 

Downstream Products

• 122624-79-7 (+/-)-cis-<4-(5-amino-7-chloro-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)-2-cyclopentenyl>carbinol 
• 118237-87-9 cis-(+/-)-2-Amino-6-chloro-9-<4-(hydroxymethyl)-2-cyclopenten-1-yl>-9H-purine 
• 118353-05-2 (+/-)-cis-2-amino-1,9-dihydro-9-[4-(hydroxymethyl)-2-cyclopenten-1-yl]-6H-purin-6-one 
• 118237-88-0 (+/-)-cis-<4-(2,6-diamino-9H-purin-9-yl)-2-cyclopentenyl>carbinol 
• 122624-83-3 (+/-)-cis-<4-(5,7-diamino-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)-2-cyclopentenyl>carbinol 
• 122624-81-1 (+/-)-cis-5-amino-3,6-dihydro-3-<4-(hydroxymethyl)-2-cyclopentenyl>-7H-1,2,3-triazolo<4,5-d>pyrimidin-7-one 

Relevant articles and documents

Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosides

(±)-cis-[4-[(2,5-Diamino-6-chloropyrimidinyl)amino]-2-cyclopentenyl]c arbinol (5a) was synthesized from 2-amino-4,6-dichloropyrimidine and cis-4-(hydroxymethyl)cyclopenteylamine (2a) by subsequent preparation of the 5-[(4-chlorophenyl)azo] derivative of t