16524-13-3 Usage
Description
(1R,2R)-2-BENZOYLAMINO-CYCLOHEXANECARBOXYLIC ACID is a cyclic chemical compound with the molecular formula C15H17NO3. It features a benzoylamine group and a carboxylic acid group, which contribute to its potential pharmaceutical applications. Due to its structural properties and functional groups, it may be utilized in the development of pharmaceutical drugs or as a component in organic synthesis. Further research and testing are required to explore its full potential and effects.
Uses
Used in Pharmaceutical Industry:
(1R,2R)-2-BENZOYLAMINO-CYCLOHEXANECARBOXYLIC ACID is used as a potential pharmaceutical candidate for the development of drugs. Its unique structure and functional groups make it a promising compound for creating new medications.
Used in Organic Synthesis:
In the field of organic synthesis, (1R,2R)-2-BENZOYLAMINO-CYCLOHEXANECARBOXYLIC ACID serves as a building block for creating more complex molecules. Its versatility in chemical reactions allows it to be a valuable component in synthesizing a variety of organic compounds.
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.
16524-13-3Relevant 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.
