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59601-91-1

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59601-91-1 Usage

Description

5,6-dinitro-1H-indazole is an organic compound characterized by its light yellow solid appearance. It is primarily known for its utility in various organic synthesis processes, making it a valuable component in the field of chemistry.

Uses

Used in Organic Synthesis:
5,6-dinitro-1H-indazole is used as a synthetic building block for the creation of various organic compounds. Its unique chemical structure allows it to be a versatile component in the synthesis of a wide range of molecules, contributing to the development of new materials and substances.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5,6-dinitro-1H-indazole is utilized as a key intermediate in the development of novel drugs. Its chemical properties make it suitable for the synthesis of potential therapeutic agents, which can be further modified and optimized for specific medical applications.
Used in Chemical Research:
5,6-dinitro-1H-indazole also plays a significant role in chemical research, where it is employed as a model compound to study various reaction mechanisms and explore new synthetic pathways. This contributes to the advancement of knowledge in organic chemistry and the discovery of innovative chemical processes.
Used in Material Science:
5,6-dinitro-1H-indazole is also used in material science as a component in the development of new materials with specific properties. Its incorporation into different molecular structures can lead to the creation of materials with unique characteristics, such as improved stability, reactivity, or selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 59601-91-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,6,0 and 1 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59601-91:
(7*5)+(6*9)+(5*6)+(4*0)+(3*1)+(2*9)+(1*1)=141
141 % 10 = 1
So 59601-91-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H4N4O4/c12-10(13)6-1-4-3-8-9-5(4)2-7(6)11(14)15/h1-3H,(H,8,9)

59601-91-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 5,6-dinitroindazole

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:59601-91-1 SDS

59601-91-1Upstream product

59601-91-1Relevant articles and documents

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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