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N-Ethyl[4,4'-sulfonylbis(benzenamine)] is a chemical compound with the molecular formula C16H18N2O2S. It is an organic compound that belongs to the class of sulfonamides, which are derivatives of benzene containing a sulfonamide functional group. This particular compound features a sulfonyl group (-SO2-) connecting two aniline (benzenamine) units, with an ethyl group attached to the nitrogen atom of one of the aniline units. It is known for its potential applications in the synthesis of dyes and pharmaceuticals, as well as its use as an intermediate in the production of certain chemical compounds. Due to its complex structure and specific functional groups, N-Ethyl[4,4'-sulfonylbis(benzenamine)] exhibits unique chemical properties and reactivity, making it an important compound in various industrial and research applications.

3572-34-7

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3572-34-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3572-34-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,7 and 2 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 3572-34:
(6*3)+(5*5)+(4*7)+(3*2)+(2*3)+(1*4)=87
87 % 10 = 7
So 3572-34-7 is a valid CAS Registry Number.
InChI:InChI=1/C14H16N2O2S/c1-2-16-12-5-9-14(10-6-12)19(17,18)13-7-3-11(15)4-8-13/h3-10,16H,2,15H2,1H3

3572-34-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[4-(ethylamino)phenyl]sulfonylaniline

1.2 Other means of identification

Product number -
Other names 4-Aminophenyl-4'-ethylaminophenylsulfon

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:3572-34-7 SDS

3572-34-7Downstream Products

3572-34-7Relevant 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.

Experimental and Theoretical Study of Electronic Substituent Effects in 4-Aminoaryl (4-Substituted Aryl) Sulphones

Benedetti, Pier G. De,Folli, Ugo,Iarossi, Dario,Frassineti, Chiara

, p. 1527 - 1532 (2007/10/02)

Substituent effects on the electronic structure of 23 biologically active 4-aminoaryl (4-substituted aryl) sulphones were investigated by means of 1H n.m.r., 13C n.m.r., and i.r. spectroscopy, as well as by semiempirical all-valence CNDO/2 calculations, w

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