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101-22-4

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101-22-4 Usage

General Description

Urea, N,N'-bis(3-aminophenyl)-, is a chemical compound with a molecular structure characterized by two 3-aminophenyl groups linked by a urea bridge. It holds significance in the field of organic chemistry and materials science, serving as a building block for the synthesis of various organic molecules and polymers. The presence of amino groups on the phenyl rings enhances its reactivity and makes it valuable in the creation of functionalized compounds with diverse applications, including pharmaceuticals, dyes, and specialty chemicals. Its ability to participate in versatile chemical reactions allows for the design and development of complex molecules with tailored properties, contributing to advancements in various industrial and scientific disciplines.

Check Digit Verification of cas no

The CAS Registry Mumber 101-22-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,0 and 1 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 101-22:
(5*1)+(4*0)+(3*1)+(2*2)+(1*2)=14
14 % 10 = 4
So 101-22-4 is a valid CAS Registry Number.

101-22-4SDS

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 1,3-bis(3-aminophenyl)urea

1.2 Other means of identification

Product number -
Other names N,N'-Bis-(3-amino-phenyl)-harnstoff

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:101-22-4 SDS

101-22-4Relevant articles and documents

Discovery of the first small molecule inhibitor of human DDX3 specifically designed to target the RNA binding site: Towards the next generation HIV-1 inhibitors

Radi, Marco,Falchi, Federico,Garbelli, Anna,Samuele, Alberta,Bernardo, Vincenzo,Paolucci, Stefania,Baldanti, Fausto,Schenone, Silvia,Manetti, Fabrizio,Maga, Giovanni,Botta, Maurizio

supporting information; experimental part, p. 2094 - 2098 (2012/04/17)

Efficacy of currently approved anti-HIV drugs is hampered by mutations of the viral enzymes, leading invariably to drug resistance and chemotherapy failure. Recent data suggest that cellular co-factors also represent useful targets for anti-HIV therapy. H

An 'inside-out' approach to suramin analogues

McGeary, Ross P.,Bennett, Andrew J.,Tran, Quoc B.,Prins, Johannes,Ross, Benjamin P.

experimental part, p. 3990 - 3997 (2009/10/09)

An approach to the synthesis of suramin analogues has been realised, which avoids synthetic problems associated with conventional routes. The use of isobutyl ester protecting groups for sulfonic acids was crucial to the success of the strategy, because these were able to be cleanly deprotected with sodium iodide, yielding the sodium salts of the corresponding sulfonic acids.

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