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2-(4-aminophenylsulfonamido)ethyl bromide is a chemical compound with the molecular formula C8H11BrN2O2S. It is a derivative of sulfonamide, which is a class of antibiotics that inhibit bacterial growth by competing with para-aminobenzoic acid (PABA) for the active site of the enzyme dihydropteroate synthase. 2-(4-aminophenylsulfonamido)ethyl bromide features a 4-aminophenylsulfonamide group attached to an ethyl chain, with a bromine atom at the 2-position. It is a white crystalline solid and is soluble in water and organic solvents. Due to its chemical structure, it has potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as in the development of new sulfonamide-based drugs. However, it is important to note that the compound's specific properties, reactivity, and potential uses should be further investigated through experimental studies and toxicological assessments.

83626-73-7

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83626-73-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83626-73-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,6,2 and 6 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83626-73:
(7*8)+(6*3)+(5*6)+(4*2)+(3*6)+(2*7)+(1*3)=147
147 % 10 = 7
So 83626-73-7 is a valid CAS Registry Number.

83626-73-7Downstream Products

83626-73-7Relevant academic research and scientific papers

Synthesis of ω-(4-aminophenylsulfonamido)alkyl disulfides and thiosulfates and their activity against dihydropteroate synthetase from sulfanilamide-resistant Neisseria gonorrhoeae

Foye,Kauffman,Suttimool

, p. 799 - 802 (1982)

A series of ω-(4-aminophenylsulfonamido)alkyl disulfides and ω-(4-aminophenylsulfonamido)alkanethiosulfates was synthesized from the reaction of p-acetamidobenzenesulfanilyl chloride and either the aminoalkyl disulfide dihydrobromide or the aminoalkyl bro

Design, synthesis, and pharmacological evaluation of multitarget-directed ligands with both serotonergic subtype 4 receptor (5-HT4R) partial agonist and 5-HT6R antagonist activities, as potential treatment of Alzheimer's disease

Yahiaoui, Samir,Hamidouche, Katia,Ballandonne, Céline,Davis, Audrey,De Oliveira Santos, Jana Sopkova,Freret, Thomas,Boulouard, Michel,Rochais, Christophe,Dallemagne, Patrick

, p. 283 - 293 (2016/07/06)

5-HT4 receptor (5-HT4R) activation and blockade of the 5-HT6 receptor (5-HT6R) are known to enhance the release of numerous neurotransmitters whose depletion is implicated in Alzheimer's disease (AD). Furthermor

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