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1H-INDAZOLE-7-CARBOXYLIC ACID, 3-BROMOis a chemical compound with the molecular formula C9H6BrN3O2. It is a derivative of indazole, a heterocyclic aromatic organic compound. This chemical has potential pharmaceutical and medicinal applications due to its involvement in the synthesis of various organic compounds and pharmaceutical intermediates. Its bromine substituent makes it a valuable building block for the synthesis of biologically active molecules and pharmaceuticals. Additionally, it has been studied for its potential anti-inflammatory and anti-cancer properties, making it a versatile compound for drug discovery and development.

1040101-01-6

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1040101-01-6 Usage

Uses

Used in Pharmaceutical Industry:
1H-INDAZOLE-7-CARBOXYLIC ACID, 3-BROMOis used as a pharmaceutical intermediate for the synthesis of various organic compounds and pharmaceuticals. Its bromine substituent makes it a valuable building block in the development of biologically active molecules.
Used in Drug Discovery and Development:
1H-INDAZOLE-7-CARBOXYLIC ACID, 3-BROMOis used as a compound with potential anti-inflammatory and anti-cancer properties. It is being studied for its potential applications in the development of new drugs for the treatment of various diseases, particularly those related to inflammation and cancer.

Check Digit Verification of cas no

The CAS Registry Mumber 1040101-01-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,0,1,0 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1040101-01:
(9*1)+(8*0)+(7*4)+(6*0)+(5*1)+(4*0)+(3*1)+(2*0)+(1*1)=46
46 % 10 = 6
So 1040101-01-6 is a valid CAS Registry Number.

1040101-01-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-bromo-2H-indazole-7-carboxylic acid

1.2 Other means of identification

Product number -
Other names 3-Bromo-1H-indazole-7-carboxylic acid

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:1040101-01-6 SDS

1040101-01-6Upstream product

1040101-01-6Downstream Products

1040101-01-6Relevant academic research and scientific papers

Inhibitory effects of a series of 7-substituted-indazoles toward nitric oxide synthases: Particular potency of 1H-indazole-7-carbonitrile

Cottyn, Betty,Acher, Francine,Ramassamy, Booma,Alvey, Luke,Lepoivre, Michel,Frapart, Yves,Stuehr, Dennis,Mansuy, Daniel,Boucher, Jean-Luc,Vichard, Dominique

, p. 5962 - 5973 (2008/12/23)

A series of new 7-monosubstituted and 3,7-disubstituted indazoles have been prepared and evaluated as inhibitors of nitric oxide synthases (NOS). 1H-Indazole-7-carbonitrile (6) was found equipotent to 7-nitro-1H-indazole (1) and demonstrated preference for constitutive NOS over inducible NOS. By contrast, 1H-indazole-7-carboxamide (8) was slightly less potent but demonstrated a surprising selectivity for the neuronal NOS. Further substitution of 6 by a Br-atom at carbon-3 of the heterocycle enhanced 10-fold the inhibitory effects. Inhibition of NO formation by 6 appeared to be competitive versus both substrate and the cofactor (6R)-5,6,7,8-tetrahydro-l-biopterin (H4B). In close analogies with 1, compound 6 strongly inhibited the NADPH oxidase activity of nNOS and induced a spin state transition of the heme-FeIII. Our results are explained with the help of the X-ray structures that identified key-features for binding of 1 at the active site of NOS.

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