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(4-amino-phenyl)-(4-isobutylamino-phenyl)-sulfone is a complex organic compound characterized by its unique molecular structure. It features a central sulfone group, which is a sulfur dioxide molecule (SO2) bonded to two carbon atoms. One of these carbon atoms is part of a 4-amino-phenyl group, which includes a phenyl ring (a six-carbon aromatic ring) with an amino group (-NH2) attached to the fourth carbon position. The other carbon atom is part of a 4-isobutylamino-phenyl group, which also has a phenyl ring but with an isobutylamine group (a branched-chain alkylamine) attached to the fourth carbon position. (4-amino-phenyl)-(4-isobutylamino-phenyl)-sulfone is significant in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other specialty chemicals due to its versatile functional groups.

6052-22-8

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6052-22-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6052-22-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,5 and 2 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6052-22:
(6*6)+(5*0)+(4*5)+(3*2)+(2*2)+(1*2)=68
68 % 10 = 8
So 6052-22-8 is a valid CAS Registry Number.

6052-22-8Downstream Products

6052-22-8Relevant academic research and scientific papers

Studies on 2,3,N,N'-substituted 4,4'-diaminodiphenylsulfones as potential antimalarial agents

Saxena,Saxena,Raina,Chandra,Sen,Anand,Seydel,Wiese

, p. 1081 - 1084 (2007/10/02)

A series of new 4,4'-diaminodiphenylsulfones substituted at 2 and 3 position and also at primary amino group of the phenyl rings have been synthesised and evaluated for their antimalarial activity against Plasmodium berghei infection in mice. Some of these compounds were active and showed complete inhibition of parasitaemia which included 7a1-7a4, 7b3, 7b4 and 16a at 1 mg/kg i.p. for 4 days and 16a, at 0.3 mg/kg for 4 days. Some compounds tested for their synthetase inhibitory action in cell-free system isolated from P. berghei (7b1, 7b2 and 8b2) were found to be more active than diaminodiphenylsulphone. The difference in order of activity between these in vivo and in vitro tests may be due to differences in their pharmacokinetic properties.

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