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Aethyl-(2-nitrophenyl)-sulfon, also known as ethyl 2-nitrophenyl sulfone, is an organic compound with the chemical formula C8H9NO4S. It is a yellow crystalline solid that is soluble in organic solvents such as ethanol and acetone. Aethyl-(2-nitrophenyl)-sulfon is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and dyes. It is also known for its potential applications in the production of sulfonamide antibiotics and other sulfonated compounds. Due to its reactivity and the presence of a nitro group, it is important to handle this chemical with care, as it may pose certain health and environmental risks.

2976-33-2

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2976-33-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2976-33-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,7 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2976-33:
(6*2)+(5*9)+(4*7)+(3*6)+(2*3)+(1*3)=112
112 % 10 = 2
So 2976-33-2 is a valid CAS Registry Number.

2976-33-2Relevant academic research and scientific papers

149. Notizen zur Synthese von 2-Aminophenylsulfonen

Courtin, Alfred,Tobel, Hans-Rudolf von,Auerbach, Guenther

, p. 1412 - 1419 (2007/10/02)

Syntheses of the alkyl, cycloalkyl and aryl 2-aminophenyl sulfones 10 were achieved by oxidation of the corresponding 2-nitrophenyl sulfides 7 to the 2-nitrophenyl sulfones 9 followed by ethanolic Bechamp-reduction.The sulfides 7 in turn were obtained by either reactions of 2-nitro-thiophenol (8) with the appropriate alkyl and cycloalkyl halides or of 2-chloro-nitrobenzene (5) with the relevant thiols.Condensation of 2-nitrobenzenesulfinic acid (3) with bromoacetic acid in aqueous alkaline solution led - presumably via 2-nitrophenylsulfonylacetic acid (4) - to methyl2-nitrophenyl sulfone (1), reduction of which gave 2-aminophenyl methyl sulfone (2).Treatment of 2-aminothiophenol (11) with t-butyl alcohol in aqueous sulfuric acid gave 2-aminophenyl t-butyl sulfide (12), which was acetylated to o-t-butylthio-acetanilide (13).Oxidation of the latter to o-t-butylsulfonyl-acetanilide (14) followed by hydrolysis led to 2-aminophenyl t-butyl sulfone (15).

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