914221-64-0 Usage
Uses
Used in Pharmaceutical Industry:
Methyl 4-chloro-2-(N-methyl-N-phenylsulphonamide)benzoate is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs. Its unique structure allows for the creation of a variety of organic compounds that can be utilized in medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, Methyl 4-chloro-2-(N-methyl-N-phenylsulphonamide)benzoate serves as an intermediate in the synthesis of agrochemicals, playing a crucial role in the development of pesticides and other agricultural chemicals that are essential for crop protection and yield enhancement.
Safety Considerations:
It is important to handle Methyl 4-chloro-2-(N-methyl-N-phenylsulphonamide)benzoate with care and adhere to the appropriate safety protocols when working with it in a laboratory setting to ensure the safety of both the personnel and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 914221-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,4,2,2 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 914221-64:
(8*9)+(7*1)+(6*4)+(5*2)+(4*2)+(3*1)+(2*6)+(1*4)=140
140 % 10 = 0
So 914221-64-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H14ClNO4S/c1-17(12-6-4-3-5-7-12)22(19,20)14-10-11(16)8-9-13(14)15(18)21-2/h3-10H,1-2H3
914221-64-0Relevant academic research and scientific papers
Synthetic method of 4-chloro-2-(N-methyl-N-phenyl sulfamoyl) methyl benzoate
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, (2016/11/07)
The invention provides a synthetic method of 4-chloro-2-(N-methyl-N-phenyl sulfamoyl) methyl benzoate. The technical scheme is that 4-chloro-2-aminobenzoic acid is taken as a raw material and has an esterification reaction, a product is subjected to diazotization and the Sandmeyer reaction, methyl 4-chloro-2-(chlorosulfonyl)benzoate is prepared and subjected to condensation with N-methylaniline, and 4-chloro-2-(N-methyl-N-phenyl sulfamoyl) methyl benzoate is obtained. The synthetic method has the advantages of conciseness, high efficiency, mild conditions, no need of purification of an intermediate and simple operation, the total yield of three steps of reactions is as high as 65%, and the method is quite suitable for industrial production.
