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4-acetylamino-2-chloro-benzenesulfonyl chloride is a chemical compound with the molecular formula C8H7ClN2O3S. It is a derivative of benzenesulfonyl chloride, featuring a chloro group at the 2-position, an acetylamino group at the 4-position, and a sulfonyl chloride group. 4-acetylamino-2-chloro-benzenesulfonyl chloride is known for its reactivity and is often used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals. Its structure allows it to participate in a range of chemical reactions, such as nucleophilic substitutions and eliminations, making it a valuable building block in organic chemistry. Due to its reactivity, it is typically handled with care in a laboratory setting to avoid unwanted side reactions or hazardous conditions.

1954-95-6

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1954-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1954-95-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1954-95:
(6*1)+(5*9)+(4*5)+(3*4)+(2*9)+(1*5)=106
106 % 10 = 6
So 1954-95-6 is a valid CAS Registry Number.

1954-95-6Upstream product

1954-95-6Relevant academic research and scientific papers

Synthesis of substituted 2-(4-amino phenyl sulphonamide)thiazoles

Gupta,Phull, Manjinder Singh

, p. 967 - 969 (2007/10/03)

Various 2-(4-amino phenyl sulphonamide) thiazoles (5a-g, 6a-g) have been prepared in good yield by condensation of 5-ethoxy-4-methyl/4-phenyl 2-amino thiazole (1a and 1b) with p-acetamido benzene sulphonyl chloride derivative (2) in pyridine-acetic anhydr

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