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2,5-dinitro-2H-indazole, a nitro-substituted indazole derivative with the molecular formula C7H4N4O4, is a yellow crystalline solid. It features a benzene ring fused to a five-membered nitrogen-containing ring and is insoluble in water but soluble in organic solvents. Known for its explosive properties, 2,5-dinitro-2H-indazole is primarily utilized in the production of munitions and explosives. Additionally, it is being explored for potential pharmaceutical applications and as a precursor in organic synthesis. Due to its toxicity and potential explosive nature, careful handling and storage are essential.

31164-29-1

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31164-29-1 Usage

Uses

Used in Munitions and Explosives Industry:
2,5-dinitro-2H-indazole is used as a high-energy material for the production of munitions and explosives, leveraging its explosive properties to enhance the performance of these products.
Used in Pharmaceutical Research:
2,5-dinitro-2H-indazole is being studied as a potential pharmaceutical compound, indicating its possible use in the development of new drugs, although further research is required to determine its safety and efficacy.
Used as a Precursor in Organic Synthesis:
In the field of organic chemistry, 2,5-dinitro-2H-indazole serves as a precursor in various chemical reactions, contributing to the synthesis of other organic compounds for different applications.

Check Digit Verification of cas no

The CAS Registry Mumber 31164-29-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,1,6 and 4 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 31164-29:
(7*3)+(6*1)+(5*1)+(4*6)+(3*4)+(2*2)+(1*9)=81
81 % 10 = 1
So 31164-29-1 is a valid CAS Registry Number.

31164-29-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dinitroindazole

1.2 Other means of identification

Product number -
Other names 2,5-dinitro-2H-indazole

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:31164-29-1 SDS

31164-29-1Relevant academic research and scientific papers

INDAZOLES AND AZAINDAZOLES AS LRRK2 INHIBITORS

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Page/Page column 262, (2021/01/29)

The present invention is directed to indazole and azaindazole compounds which are inhibitors of LRRK2 and are useful in the treatment of CNS disorders.

INDAZOLES AS LRRK2 INHIBITORS

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Page/Page column 220, (2020/10/09)

The present invention is directed to indazole compounds which are inhibitors of LRRK2 and are useful in the treatment of CNS disorders.

INDAZOLE DERIVATIVES USEFUL AS MELANIN CONCENTRATING RECEPTOR LIGANDS

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Page/Page column 47-48, (2008/12/05)

The present invention relates to novel compounds, in particular, novel indazole that may be used as melanin concentrating hormone receptor ligands, methods of preparing such compounds, compositions containing such compounds, and methods of using such compounds to treat MCH related disorders.

Azoles. Part 32: Nitroindazole derivatives and their electron affinity

Usarewicz,Wrzeciono,Lukaszewski,Gatniejewska,Peisert

, p. 15 - 18 (2007/10/02)

A modified procedure for the synthesis of the dinitroindazoles 5-8 is described. Treatment of the chloronitro- and dinitroindazoles 1-8 with epichlorohydrin afforded the chlorohydroxypropyl- and epoxypropylindazole derivatives 2a-8a, 1b-5b, 7b and 7c. The structure of the compounds is confirmed by the aid of their IR, 1H and 13C NMR spectra. The electron affinity of the nitroindazole derivatives 1-16 is discussed on the basis of their halfwave potentials and in the combination with their eventual radiosensitizing properties.

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