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3,5-Dichloro-7-nitro (1H)indazole, with the chemical formula C7H3Cl2N3O2, is a nitroindazole derivative known for its antibacterial and antifungal properties. 3,5-DICHLORO-7-NITRO (1H)INDAZOLE features a seven-membered indazole ring with two chlorine atoms and a nitro group attached, making it a versatile chemical for pharmaceutical and research applications. It has been studied for its potential in treating bacterial and fungal infections and for its role as a selective GPR109A agonist, which could have implications for metabolic and cardiovascular disorders.

316810-83-0

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316810-83-0 Usage

Uses

Used in Pharmaceutical Development:
3,5-Dichloro-7-nitro (1H)indazole is used as a research chemical for the development of new pharmaceuticals, particularly those targeting bacterial and fungal infections. Its antibacterial and antifungal properties make it a promising candidate for creating effective treatments.
Used in Metabolic and Cardiovascular Research:
As a selective GPR109A agonist, 3,5-dichloro-7-nitro (1H)indazole is used in scientific research to study the role of this receptor in metabolic and cardiovascular disorders. Understanding its interaction with GPR109A could lead to the development of new therapies for related health conditions.
Used in Antibacterial Applications:
3,5-Dichloro-7-nitro (1H)indazole is used as an antibacterial agent for treating various bacterial infections. Its ability to target and eliminate harmful bacteria makes it a valuable component in the development of new antibiotics.
Used in Antifungal Applications:
In the field of antifungal treatment, 3,5-dichloro-7-nitro (1H)indazole is used as an antifungal agent to combat fungal infections. Its effectiveness against fungi contributes to the creation of new antifungal medications and treatments.
Used in Scientific Research:
3,5-Dichloro-7-nitro (1H)indazole is utilized in various scientific research applications, including studies on its chemical properties, potential interactions with biological systems, and its role in the development of new drugs and therapies. Its versatility as a chemical compound makes it an important tool in scientific exploration.

Check Digit Verification of cas no

The CAS Registry Mumber 316810-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,8,1 and 0 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 316810-83:
(8*3)+(7*1)+(6*6)+(5*8)+(4*1)+(3*0)+(2*8)+(1*3)=130
130 % 10 = 0
So 316810-83-0 is a valid CAS Registry Number.

316810-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-dichloro-7-nitro-2H-indazole

1.2 Other means of identification

Product number -
Other names 1H-Indazole,3,5-dichloro-7-nitro

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:316810-83-0 SDS

316810-83-0Downstream Products

316810-83-0Relevant academic research and scientific papers

Research in 7-aminoindazole series: Synthesis of new halo-7H-4-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-6-ones and 5H-9-halo-6-methylpyrazolo[1,5,4-ef][1,5]benzodiazepin-4-ones

Rakib,Benchidmi,Essassi,El Bouadili,Ibn Mansour,Bellan,Lopez,Lamande

, p. 339 - 345 (2007/10/03)

A new class of 7-aminohaloindazoles has been synthesized. Reactivity of the amino groups of these bicyclic systems has been investigated. The halogenated pyrazolo-1,5-benzodiazepinones have been synthesized by the condensation of 7-aminoindazoles with ethyl acetoacetate.

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