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81131-39-7

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81131-39-7 Usage

Description

Cyclohexanecarboxylic acid, 3-amino-, (1R,3S)(9CI) is a chemical compound characterized by its molecular formula C8H15NO2. It is a stereoisomer of cyclohexanecarboxylic acid, featuring an amino group attached to the third carbon atom in a 1R,3S configuration. Cyclohexanecarboxylic acid, 3-amino-, (1R,3S)(9CI) is utilized in a range of chemical and pharmaceutical applications, serving as a building block for synthesizing other organic compounds and being investigated for its potential medicinal properties and biological activity, particularly in drug development and research.

Uses

Used in Chemical Synthesis:
Cyclohexanecarboxylic acid, 3-amino-, (1R,3S)(9CI) is used as a building block in chemical synthesis for creating a variety of organic compounds. Its unique structure allows for the development of new molecules with specific properties and functions, contributing to the advancement of the chemical industry.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, Cyclohexanecarboxylic acid, 3-amino-, (1R,3S)(9CI) is utilized for its potential medicinal properties and biological activity. It may serve as a key component in the development of new drugs, particularly those targeting specific medical conditions or diseases.
Used in Drug Development and Research:
Cyclohexanecarboxylic acid, 3-amino-, (1R,3S)(9CI) is also studied in drug development and research for its potential to contribute to the creation of innovative medications. Its unique stereochemistry and functional groups make it a valuable candidate for exploring novel therapeutic approaches and enhancing the effectiveness of existing treatments.

Check Digit Verification of cas no

The CAS Registry Mumber 81131-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,3 and 1 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81131-39:
(7*8)+(6*1)+(5*1)+(4*3)+(3*1)+(2*3)+(1*9)=97
97 % 10 = 7
So 81131-39-7 is a valid CAS Registry Number.

81131-39-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Cyclohexanecarboxylic acid, 3-amino-, (1R,3S)- (9CI)

1.2 Other means of identification

Product number -
Other names (1R,3S)-3-Amino-cyclohexanecarboxylic 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:81131-39-7 SDS

81131-39-7Relevant articles and documents

An improved synthesis of (1R,3S)-3-[(tert-butoxycarbonyl)amino] cyclohexanecarboxylic acid

Badland, Matthew,Bains, Carol A.,Howard, Roger,Laity, Daniel,Newman, Sandra D.

experimental part, p. 864 - 866 (2010/11/02)

An improved synthesis of (1R,3S)-3-[(tert-butoxycarbonyl)amino] cyclohexanecarboxylic acid from 3-aminobenzoic acid is described utilising milder and more selective conditions. Both a classical salt resolution and an enzymatic approach have been shown to give the desired compound in high selectivity.

Substituted pyrroles suitable for continuous infusion

-

, (2008/06/13)

Disclosed are novel substituted pyrroles having the formula These compounds and their pharmaceutically acceptable salts are suitable for administration to patients as continuous infusion solution and are useful in the treatment and/or control of cell prol

2-aminopyridine derivatives and combinatorial libraries thereof

-

, (2008/06/13)

The present invention relates to novel 2-aminopyridine derivative compounds of the following formula: wherein R1to R5have the meanings provided herein. The invention further relates to combinatorial libraries containing two or more such compounds, as well as methods of preparing 2-aminopyridine derivative compounds.

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