29331-43-9 Usage
Description
(1-chloro-3-cyano-propan-2-yl) acetate, with the chemical formula C6H8ClNO2, is a colorless liquid characterized by a sharp, pungent odor. This chemical compound serves as a versatile intermediate in the synthesis of various products, including pharmaceuticals, agrochemicals, and fine chemicals.
Uses
Used in Pharmaceutical Industry:
(1-chloro-3-cyano-propan-2-yl) acetate is used as a synthetic intermediate for the production of pharmaceuticals, playing a crucial role in the development of new medications and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, (1-chloro-3-cyano-propan-2-yl) acetate is utilized as an intermediate in the synthesis of various agrochemicals, contributing to the creation of products that enhance crop protection and yield.
Used in Fine Chemicals Synthesis:
(1-chloro-3-cyano-propan-2-yl) acetate is also employed as an intermediate in the synthesis of fine chemicals, which are essential in a wide range of applications, from fragrances to dyes.
Used as a Solvent:
(1-chloro-3-cyano-propan-2-yl) acetate functions as a solvent in various chemical processes, facilitating reactions and improving the efficiency of production methods.
Used in Plasticizers and Polymers Production:
Furthermore, it is used in the production of plasticizers and polymers, which are vital components in the manufacturing of plastics and other materials with diverse applications.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 29331-43-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,9,3,3 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 29331-43:
(7*2)+(6*9)+(5*3)+(4*3)+(3*1)+(2*4)+(1*3)=109
109 % 10 = 9
So 29331-43-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H8ClNO2/c1-5(9)10-6(4-7)2-3-8/h6H,2,4H2,1H3
29331-43-9Relevant articles and documents
Preparation of (R)- and (S)-4-chloro-3-acetoxybutyronitrile using microbial resolution
Idogaki, Hideaki,Kasai, Naoya,Takeuchi, Motoko,Hatada, Miki,Suzuki, Toshio
, p. 369 - 373 (2007/10/03)
A new preparation of optically active 4-chloro-3-acetoxybutyronitrile (AcBN) was developed using the resting cells of bacteria. The resolution was based on enantioselective hydrolysis of the ester function of the substrate. (R)-AcBN was prepared using Pseudomonas sp. DS-K-717, and the resulting (R)-AcBN was obtained with high enantiomeric excess of >98% with a yield of 36% during the microbial resolution step. (S)-AcBN was prepared in the same manner using the resting cells of Pseudomonas sp. DS-K-19 and showed a high enantiomeric excess of >98% with a yield of 32%. The enzyme activity was enhanced and induced by the addition of AcBN, particularly the (R)-ester hydrolysis, which was enhanced 20-fold.
