123288-54-0

Basic information

• Product Name: (+/-)-cis-3-aminocyclopentanemethanol
• CAS NO: 123288-54-0
• Molecular Weight: 115.175
• Mol File: 123288-54-0.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 197.3±13.0 °C(Predicted)
• Density: 1.002±0.06 g/cm3(Predicted)
• CAS DataBase Reference: (+/-)-cis-3-aminocyclopentanemethanol(CAS DataBase Reference)
• NIST Chemistry Reference: (+/-)-cis-3-aminocyclopentanemethanol(123288-54-0)
• EPA Substance Registry System: (+/-)-cis-3-aminocyclopentanemethanol(123288-54-0)

Safety Data

• Hazardous Substances Data: 123288-54-0(Hazardous Substances Data)

Usage

General Description

(+/-)-cis-3-aminocyclopentanemethanol, also known as ACPCM, is a chemical compound with a cyclopentane ring structure and an amino group attached to the third carbon atom. (+/-)-cis-3-aminocyclopentanemethanol exists as a racemic mixture of two stereoisomers, and its chiral nature imparts unique properties that make it a valuable building block for pharmaceuticals and agrochemicals. ACPCM has been studied for its potential as a versatile intermediate for the synthesis of various biologically active compounds. It is of interest for its potential use in the development of new drugs and as a key component in the creation of diverse chemical structures with potential biological activities. Additionally, the compound's cyclopentane ring provides stability and structural versatility, making it a valuable molecule for the synthesis of complex organic compounds.

Upstream product

• 116595-43-8 (+/-)-cis methyl 3-(aminocarbonyl)cyclopentanecarboxylate 
• 876-05-1 cis-1,3-cyclopentanedicarboxylic acid 
• 6054-16-6 cis-1,3-cyclopentanedicarboxylic acid anhydride 
• 116940-85-3 (+/-)-cis-3-(hydroxymethyl)cyclopentanecarboxamide 
• 61865-50-7 Acetic acid 4-acetylamino-cyclopent-2-enylmethyl ester 
• 65898-98-8 Acetic acid 3-acetylamino-cyclopentylmethyl ester 
• 84545-00-6 (+/-)-(1S,3R)-3-(methoxycarbonyl)cyclopentanecarboxylic acid 
• 85174-63-6 (+/-)-methyl cis-3-(chloromethanoyl)cyclopentanecarboxylate 

Downstream Products

• 122624-76-4 (+/-)-cis-<3-<<2-amino-6-chloro-5-<(4-chlorophenyl)azo>-4-pyrimidinyl>amino>cyclopentyl>carbinol 
• 122624-71-9 (+/-)-cis-<3-(5,7-diamino-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)cyclopentyl>carbinol 
• 122624-82-2 (+/-)-cis-5-amino-3,6-dihydro-3-<3-(hydroxymethyl)cyclopentyl>-1,2,3-triazolo<4,5-d>pyrimidin-7-one 
• 122624-80-0 (+/-)-cis-<3-(5-amino-7-chloro-3H-1,2,3-triazolo<4,5-d>pyrimidin-3-yl)cyclopentyl>carbinol 
• 118237-86-8 (+/-)-cis-<3-(2-amino-6-chloro-9H-purin-9-yl)cyclopentyl>carbinol 
• 112915-00-1 (+/-)-cis-2-amino-1,9-dihydro-9-<3-(hydroxymethyl)cyclopent-1-yl>-6H-purin-6-one 
• 120330-36-1 (+/-)-cis-<3-(2,6-diamino-9H-purin-9-yl)cyclopentyl>carbinol 
• 116891-16-8 (+/-)-1--5-methyl-2,4(1H,3H)-pyrimidinedione benzoate 
• 116891-20-4 (+/-)-1--2,4(1H,3H)-pyrimidinedione benzoate 
• 116891-18-0 (+/-)-2,3-dihydro-1--2-thioxo-4(1H)-pyrimidinone benzoate 
• 116940-94-4 Benzoic acid (1S,3R)-3-(4-chloro-5-methyl-2-oxo-2H-pyrimidin-1-yl)-cyclopentylmethyl ester 
• 116940-95-5 Benzoic acid (1S,3R)-3-(4-chloro-2-oxo-2H-pyrimidin-1-yl)-cyclopentylmethyl ester 
• 78795-25-2 (+/-)-1--5-methyl-2,4(1H,3H)-pyrimidinedione 

Relevant articles and documents

Sulfonamide derivatives

A sulfonamide derivative of the general formula: wherein, R1 represents (i) COOR11, (ii) CH2 OR12 or (iii) CONR13 R14, Tx--represents STR1 Xb represents (i) bond, (ii) alkylene group of from 1 to 4 carbon atoms or (iii) alkenylene group of from 2 to 4 carbon atoms (with the proviso that --CH=CHCH2 -- and --CH2 CH=CHCH2 -- are excluded), R2b represents (i) hydrogen atom, (ii) halogen atom or (iii) alkyl group of from 1 to 4 carbon atom(s), posses an antagonistic activity on TXA2.

Synthesis of cyclopentane analogs of 1-(2',3'-dideoxy-β-glycero-pentofuranosyl)pyrimidine nucleosides

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