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53347-49-2

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53347-49-2 Usage

Description

2,2'-Diamino[sulfonylbisbenzene], also known as Bis(2-aminophenyl) Sulfone, is an organic compound with the molecular formula C12H12N2O2S. It is a derivative of benzene with two amino groups attached to the para positions and a sulfonyl group connecting the two benzene rings. 2,2'-Diamino[sulfonylbisbenzene] is known for its involvement in various physical, engineering, and chemical processes.

Uses

Used in Chemical and Engineering Processes:
2,2'-Diamino[sulfonylbisbenzene] is used as an intermediate in the synthesis of various chemical compounds and materials. Its unique structure allows it to be a versatile building block for the development of new molecules with specific properties and applications.
Used in Quality Control:
In the field of quality control, 2,2'-Diamino[sulfonylbisbenzene] is used for the preparation and analysis of diamino di-Ph sulfone. High-performance liquid chromatography (HPLC) is employed to ensure the purity and consistency of the final product, which is crucial for its performance in various applications.
Used in Pharmaceutical Industry:
2,2'-Diamino[sulfonylbisbenzene] is used as a key component in the development of pharmaceutical compounds. Its unique chemical structure allows it to be modified and functionalized to create new drugs with specific therapeutic properties.
Used in Material Science:
In material science, 2,2'-Diamino[sulfonylbisbenzene] is used as a building block for the development of new materials with tailored properties. Its incorporation into polymers and other materials can lead to improved mechanical, thermal, and chemical properties, making it suitable for various applications, such as coatings, adhesives, and composites.

Check Digit Verification of cas no

The CAS Registry Mumber 53347-49-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,3,4 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53347-49:
(7*5)+(6*3)+(5*3)+(4*4)+(3*7)+(2*4)+(1*9)=122
122 % 10 = 2
So 53347-49-2 is a valid CAS Registry Number.

53347-49-2SDS

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 2-(2-aminophenyl)sulfonylaniline

1.2 Other means of identification

Product number -
Other names 2.2'-Diamino-diphenylsulfon

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:53347-49-2 SDS

53347-49-2Relevant articles and documents

Inhibitors of kynureninase

-

, (2008/06/13)

The present invention provides inhibitors of kynureninase having the formula STR1 where X is CHOH, S, SO2, SO, SONH, PO2 H or PONH2, RA and RB, independently of one another, are H, a halogen, CF3

3H-Azepines and Related Systems. Part 2. The Photolyses of Aryl Azides Bearing Electron-withdrawing Substituents

Purvis, Roger,Smalley, Robert K.,Suschitzky, Hans,Alkhader, Mohamed A.

, p. 249 - 254 (2007/10/02)

The photolyses of ortho-substituted aryl azides (o-XC6H4N3 where X = CONHNH2, CONHN=CHAr, NO2, CN, CF3, SO2OMe, SO2NH2, or SO2Ph) in methanol-tetrahydrofuran solution are described.With X = CF3 or CONHN=CHAr, 3-substituted 2-methoxy-3H-azepines are products, while in other cases polymeric products, amines or mixtures of isomeric azepines are obtained.The product from the photolysis of o-azidophenyl phenyl sulphoxide (X = SOPh) is identified tentatively (n.m.r. evidence) as 7-methoxy-2-phenylsulphinyl-3H-azepine.In contrast, methyl p-azidobenzoate and p-cyanophenyl azide yield the corresponding 5-substituted 2-methoxy-3H-azepines, whereas methyl m-azidobenzoate yields only methyl 2-methoxy-3H-azepine-6-carboxylate.Irradiation of methyl o-azidobenzoate in aqueous tetrahydrofuran gives 1,3-dihydro-3-methoxycarbonyl-2H-azepin-2-one.

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