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4-methyl-N-(2-ethylbutyryl)benzenesulfonamide is a chemical compound with the molecular formula C13H19NO2S. It is a derivative of benzenesulfonamide, featuring a methyl group at the 4-position and a 2-ethylbutyryl group attached to the nitrogen atom. 4-methyl-N-(2-ethylbutyryl)benzenesulfonamide is an organic molecule that belongs to the class of sulfonamides, which are known for their diverse applications in various fields, including pharmaceuticals and agrochemicals. The 2-ethylbutyryl group, a branched-chain acyl group, contributes to the compound's specific properties and potential uses. While the exact applications of this particular compound are not specified, sulfonamides in general are known for their antimicrobial activity, which has led to their use as antibiotics and in the synthesis of other pharmaceuticals. The compound's structure and properties make it a candidate for further research and development in these areas.

1788-14-3

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1788-14-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1788-14-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,8 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1788-14:
(6*1)+(5*7)+(4*8)+(3*8)+(2*1)+(1*4)=103
103 % 10 = 3
So 1788-14-3 is a valid CAS Registry Number.

1788-14-3Downstream Products

1788-14-3Relevant academic research and scientific papers

Mild decarboxylative activation of malonic acid derivatives by 1,1′-carbonyldiimidazole

Lafrance, Danny,Bowles, Paul,Leeman, Kyle,Rafka, Robert

supporting information; experimental part, p. 2322 - 2325 (2011/06/26)

Chemical equations presented. Malonic acid derivatives undergo unusually mild decarboxylation when treated with N,N′-carbonyldiimidazole (CDI) at room temperature to generate the carbonyl imidazole moiety in high yield, which can be reacted further with a variety of nucleophiles in an efficient one-pot process.

Sulfamidation of 2-arylaldehydes and ketones with chloramine-T

Baumann, Thomas,Bachle, Michael,Brase, Stefan

, p. 3797 - 3800 (2007/10/03)

A series of aliphatic and aromatic carbonyl compounds has been transformed into the corresponding sulfamidated products by means of amine-catalyzed nitrene transfer of chloramine-T. Depending on the residues R, either α-sulfamidation in the case of aromat

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