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4-amino-3-(2-amino-5-sulfamoyl-phenyl)disulfanyl-benzenesulfonamide is a complex organic compound with the molecular formula C12H13N5O4S3. It is characterized by the presence of an amino group (-NH2) at the 4-position, a disulfide bridge (-S-S-) connecting two phenyl rings, and a sulfonamide group (-SO2NH2) at the 3-position. The 2-amino-5-sulfamoyl-phenyl group is attached to the disulfide bridge, further enhancing the molecule's reactivity and potential applications. 4-amino-3-(2-amino-5-sulfamoyl-phenyl)disulfanyl-benzenesulfonamide is known for its potential use in the synthesis of pharmaceuticals and agrochemicals, particularly as a building block for the development of new drugs and pesticides. Its unique structure allows for a range of chemical reactions and interactions, making it a valuable component in the field of medicinal chemistry.

5332-71-8

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5332-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5332-71-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,3 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5332-71:
(6*5)+(5*3)+(4*3)+(3*2)+(2*7)+(1*1)=78
78 % 10 = 8
So 5332-71-8 is a valid CAS Registry Number.

5332-71-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-amino-3-[(2-amino-5-sulfamoylphenyl)disulfanyl]benzenesulfonamide

1.2 Other means of identification

Product number -
Other names 4,4'-Diamino-3,3'-disulfandiyl-bis-benzolsulfonsaeure-diamid

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:5332-71-8 SDS

5332-71-8Relevant academic research and scientific papers

Design, synthesis and evaluation of benzothiazole derivatives as multifunctional agents

Andreotti, Elisa,Baldisserotto, Anna,Balzarini, Jan,Buzzi, Raissa,Dissette, Valeria,Djuidje, Ernestine Nicaise,Liekens, Sandra,Manfredini, Stefano,Sciabica, Sabrina,Serra, Elena,Vertuani, Silvia

, (2020/06/22)

Oxidative stress is the product or aetiology of various multifactorial diseases; on the other hand, the development of multifunctional compounds is a recognized strategy for the control of complex diseases. To this end, a series of benzothiazole derivatives was synthesized and evaluated for their multifunctional effectiveness as antioxidant, sunscreen (filter), antifungal and antiproliferative agents. Compounds were easily synthesized via condensation reaction between 2-aminothiophenols and different benzaldehydes. SAR study, particularly in position 2 and 6 of benzothiazoles, led to the identification of 4g and 4k as very interesting potential compounds for the design of multifunctional drugs. In particular, compound 4g is the best blocker of hERG potassium channels expressed in HEK 293 cells exhibiting 60.32percent inhibition with IC50 = 4.79 μM.

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