4960-82-1 Usage
Uses
Used in Pharmaceutical Industry:
2-chloro-N-(2-chloroacetyl)acetamide is used as a synthetic intermediate for the development of various pharmaceuticals. Its role in the synthesis process is vital for creating a range of medicinal compounds that address different health conditions.
Used in Agrochemical Industry:
In the agrochemical sector, 2-chloro-N-(2-chloroacetyl)acetamide is utilized as an intermediate in the production of agrochemicals. Its contribution to the formulation of these chemicals helps in enhancing crop protection and management strategies.
Used as an Antimicrobial Agent:
2-chloro-N-(2-chloroacetyl)acetamide is employed as an antimicrobial agent across diverse applications. Its effectiveness in inhibiting the growth of microorganisms makes it suitable for use in various industries where microbial control is essential, such as in the food and beverage sector, cosmetics, and medical applications.
Used in Research and Development:
2-chloro-N-(2-chloroacetyl)acetamide also serves as a valuable asset in research and development settings. It is used in the study of chemical reactions and processes, contributing to the advancement of scientific knowledge and the discovery of new applications and uses.
Check Digit Verification of cas no
The CAS Registry Mumber 4960-82-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,9,6 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4960-82:
(6*4)+(5*9)+(4*6)+(3*0)+(2*8)+(1*2)=111
111 % 10 = 1
So 4960-82-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H5Cl2NO2/c5-1-3(8)7-4(9)2-6/h1-2H2,(H,7,8,9)
4960-82-1Relevant academic research and scientific papers
The Chemistry of Nitrilium Salts. Part 1. Acylation of Phenols and Phenol Ethers with Nitriles and Trifluoromethanesulphonic Acid
Booth, Brian L.,Noori, Ghazi F.M.
, p. 2894 - 2900 (2007/10/02)
Aliphatic nitriles, RCN (R = Me, n-Pr, CH2Cl, and CCl3), in the presence of trifluoromethanesulphonic acid have been found to react with a number of mono-, di-, and tri-substituted phenols and phenol ethers at room temperature to give ketones after hydrolysis of the reaction mixture.Moderate to good yields of acylation products are obtained in the majority of these reactions.The yield with malononitrile and succinonitrile, which are only slightly soluble in the reaction medium, are generally poor, and reaction involves only one of the available nitrile groups.Attempts to use diethyl ether and dichloromethane as solvents for some of these reactions were unsuccessful, but limited success was achieved with nitromethane.
