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5,6-DIAMINOINDAZOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

7404-68-4

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7404-68-4 Usage

Chemical Properties

Light Brown Powder

Check Digit Verification of cas no

The CAS Registry Mumber 7404-68-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,0 and 4 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7404-68:
(6*7)+(5*4)+(4*0)+(3*4)+(2*6)+(1*8)=94
94 % 10 = 4
So 7404-68-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H8N4/c8-5-1-4-3-10-11-7(4)2-6(5)9/h1-3H,8-9H2,(H,10,11)

7404-68-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1H-indazole-5,6-diamine

1.2 Other means of identification

Product number -
Other names T0512-4927

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:7404-68-4 SDS

7404-68-4Relevant academic research and scientific papers

BENZIMIDAZOLE DERIVATIVES AND PHARMACEUTICAL COMPOSITIONS AND USES THEREOF

-

Page/Page column 36, (2013/02/27)

The present invention relates to benzimidazole derivatives and their pharmaceutical compositions and uses, specifically to benzimidazole derivatives of Formula (I), or their stereoisomer, pharmaceutically acceptable salt or solvates thereof, in which R1, R2, R3, R4, R5 and n have the definitions in the description; the present invention further relates to a pharmaceutical composition containing the compounds, methods for preparing the compounds, and use of the compounds for manufacturing of a medicament for prophylaxis and/or treatment of peptic ulcer, ulcer hemorrhage and diseases associated with gastric acid.

Synthesis and biological activities of pyrazolo[3,4-g]quinoxaline derivatives

Gavara, Laurent,Saugues, Emmanuelle,Alves, Georges,Debiton, Eric,Anizon, Fabrice,Moreau, Pascale

experimental part, p. 5520 - 5526 (2010/12/20)

The synthesis of new pyrazolo[3,4-g]quinoxaline derivatives, as well as their Pim kinases (Pim-1, Pim-2, Pim-3) inhibitory potencies and in vitro antiproliferative activities toward a human fibroblast primary culture and three human solid cancer cell lines (PA1, PC3 and DU145) are described. The results obtained in this preliminary structure-activity relationship study have pointed out that most of the compounds in this series exhibited interesting in vitro Pim-3 kinase inhibitory potencies. Moreover, some of the tested compounds have demonstrated favorable antiproliferative potencies.

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