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Methyl (S)-1-(4-chlorophenyl)aziridine-2-carboxylate is a chemical compound with the molecular formula C10H10ClNO2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the "S" in its name indicates that it is the (S)-enantiomer. methyl (S)-1-(4-chlorophenyl)aziridine-2-carboxylate features a 3-membered aziridine ring, a 4-chlorophenyl group, and a carboxylate group attached to a methyl ester. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of chiral amines and other chiral compounds. Due to its potential applications in the development of drugs and pesticides, it is an important compound in the field of organic chemistry and medicinal chemistry.

4916-17-0

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4916-17-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4916-17-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,1 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4916-17:
(6*4)+(5*9)+(4*1)+(3*6)+(2*1)+(1*7)=100
100 % 10 = 0
So 4916-17-0 is a valid CAS Registry Number.

4916-17-0Downstream Products

4916-17-0Relevant academic research and scientific papers

Nitrile biotransformations for the efficient synthesis of highly enantiopure 1-arylaziridine-2-carboxylic acid derivatives and their stereoselective ring-opening reactions

Wang, Jin-Yuan,Wang, De-Xian,Zheng, Qi-Yu,Huang, Zhi-Tang,Wang, Mei-Xiang

, p. 2040 - 2045 (2007)

Catalyzed by the Rhodococcus erythropolis AJ270 whole cell catalyst under very mild conditions, biotransformations of racemic 1-arylaziridine-2- carbonitriles proceeded efficiently and enantioselectively to produce highly enantiopure S-1-arylaziridine-2-c

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