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16524-13-3

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16524-13-3 Usage

General Description

(1R,2R)-2-BENZOYLAMINO-CYCLOHEXANECARBOXYLIC ACID is a chemical compound with the molecular formula C15H17NO3. It is a cyclic compound that contains a benzoylamine group and a carboxylic acid group. (1R,2R)-2-BENZOYLAMINO-CYCLOHEXANECARBOXYLIC ACID has potential pharmaceutical applications due to its structural properties and functional groups, and it may be used in the development of pharmaceutical drugs or as a building block in organic synthesis. However, further research and testing are necessary to fully understand the potential uses and effects of (1R,2R)-2-BENZOYLAMINO-CYCLOHEXANECARBOXYLIC ACID.

Check Digit Verification of cas no

The CAS Registry Mumber 16524-13-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,5,2 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 16524-13:
(7*1)+(6*6)+(5*5)+(4*2)+(3*4)+(2*1)+(1*3)=93
93 % 10 = 3
So 16524-13-3 is a valid CAS Registry Number.

16524-13-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-benzamidocyclohexane-1-carboxylic acid

1.2 Other means of identification

Product number -
Other names trans-2-benzoylamino-1-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:16524-13-3 SDS

16524-13-3Relevant articles and documents

Synthesis and microbial transformation of β-amino nitriles

Winkler, Margit,Martínková, Ludmila,Knall, Astrid C.,Krahulec, Stefan,Klempier, Norbert

, p. 4249 - 4260 (2007/10/03)

Rhodococcus equi A4, Rhodococcus erythropolis NCIMB 11540 and Rhodococcus sp. R312 were investigated towards their ability to produce β-amino amides and acids from β-amino nitriles. The microorganisms show comparable trends: five-membered alicyclic 2-amino nitriles were transformed significantly faster than the six-membered compounds and the products of trans-2-amino nitriles (amides and acids) were formed considerably faster than the cis-counterparts (amides). The trans-five membered nitriles gave the amides (1b, 5b) in excellent enantiomeric excess (94-99%), the biotransformation of trans-six membered substrates resulted in the formation of the acid (3c, 7c) in excellent ee (87-99%). The ee's of the cis-compounds were throughout lower. Fifteen new substances were synthesized and characterized in the course of this work.

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