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49805-32-5

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49805-32-5 Usage

General Description

Cyclopentanecarboxylic acid, 3-amino-, (1R,3S)-rel- (9CI) is a chemical compound that belongs to the class of cyclopentanecarboxylic acids with an amino group attached at the third carbon atom. It exists as a stereoisomer with a specific configuration, denoted as (1R,3S)-rel-. Cyclopentanecarboxylic acid, 3-amino-, (1R,3S)-rel- (9CI) may have potential applications in pharmaceuticals, agrochemicals, and materials science due to its unique structure and properties. Further research and study are needed to fully understand the potential uses and effects of this chemical compound.

Check Digit Verification of cas no

The CAS Registry Mumber 49805-32-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,9,8,0 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 49805-32:
(7*4)+(6*9)+(5*8)+(4*0)+(3*5)+(2*3)+(1*2)=145
145 % 10 = 5
So 49805-32-5 is a valid CAS Registry Number.

49805-32-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cis-3-aminocyclopentane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names cis-3-Aminocyclopentanecarboxylic Acid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:49805-32-5 SDS

49805-32-5Relevant articles and documents

Synthesis of analogues of GABA. XV. Preparation and resolution of some potent cyclopentene and cyclopentane derivatives

Allan,Fong

, p. 855 - 864 (2007/10/02)

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Synthesis and configurational analysis of dl-myxoviromycin.

Katsube

, p. 232 - 238 (2007/10/06)

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