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7-Bromo-3-methyl-1H-indazole, a member of the indazole class of molecules, is a halogenated derivative characterized by the presence of a bromine atom at the 7th position and a methyl group at the 3rd position on the indazole ring. This chemical compound is recognized for its potential applications in pharmaceutical and research settings due to the biological activities of indazole derivatives, which include anticancer, antimicrobial, and anti-inflammatory properties. Its molecular structure and functional groups render it a valuable component for the synthesis of new compounds with possible pharmacological activity. Careful handling is advised due to the inherent risks associated with its use.

1159511-75-7

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1159511-75-7 Usage

Uses

Used in Pharmaceutical Industry:
7-Bromo-3-methyl-1H-indazole is used as a building block for the synthesis of new compounds with potential pharmacological activity, leveraging its molecular structure and functional groups to create novel therapeutic agents.
Used in Research Settings:
In research, 7-Bromo-3-methyl-1H-indazole is utilized as a chemical probe to study the biological activities of indazole derivatives, particularly focusing on their anticancer, antimicrobial, and anti-inflammatory properties. This aids in the discovery and development of new drugs with improved efficacy and safety profiles.
Used in Drug Development:
7-Bromo-3-methyl-1H-indazole is employed as a precursor in the development of new drugs, where its unique chemical properties can be harnessed to create compounds with specific therapeutic targets and mechanisms of action.
Used in Chemical Synthesis:
As a versatile chemical intermediate, 7-Bromo-3-methyl-1H-indazole is used in the synthesis of a variety of organic compounds, contributing to the advancement of chemical libraries and the exploration of new chemical space for potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1159511-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,5,1 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1159511-75:
(9*1)+(8*1)+(7*5)+(6*9)+(5*5)+(4*1)+(3*1)+(2*7)+(1*5)=157
157 % 10 = 7
So 1159511-75-7 is a valid CAS Registry Number.

1159511-75-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-bromo-3-methyl-2H-indazole

1.2 Other means of identification

Product number -
Other names 7-Bromo-3-methyl-1H-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:1159511-75-7 SDS

1159511-75-7Downstream Products

1159511-75-7Relevant academic research and scientific papers

AMIDE COMPOUND

-

Page/Page column 49; 50, (2010/03/04)

A compound having GPR52 agonist activity or a salt thereof is provided. The compound can be provided as a preventive/therapeutic agent for schizophrenia or the like. The compound is represented by the following formula: wherein A represents —CONRa— or —NRaCO—, Ra represents a hydrogen atom or the like,B represents a hydrogen atom or the like,a ring Cy1 represents a six-membered aromatic ring which may have one or more substituents in addition to a group represented by -A-B,a ring Cy2 represents a six-membered ring which may be substituted with a halogen atom or the like,a ring Cy3 represents a five- or six-membered ring which may have one or more substituents;X represents C1-2 alkylene or the like,m represents an integer of 0 to 2, anda ring Cy4 represents a six-membered aromatic ring which may have one or more substituents.

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