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90221-46-8

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90221-46-8 Usage

General Description

6-Bromo-3-methyl-1H-indazole is a chemical compound with the molecular formula C8H7BrN2. It belongs to the class of indazole derivatives and contains a bromine atom and a methyl group. This chemical compound is commonly used as a building block in organic synthesis for the preparation of various pharmaceuticals, agrochemicals, and fine chemicals. Its structure and properties make it a versatile intermediate in the production of biologically active molecules. 6-Bromo-3-methyl-1H-indazole has a wide range of applications in the pharmaceutical and chemical industries due to its unique molecular structure and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 90221-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,2,2 and 1 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90221-46:
(7*9)+(6*0)+(5*2)+(4*2)+(3*1)+(2*4)+(1*6)=98
98 % 10 = 8
So 90221-46-8 is a valid CAS Registry Number.

90221-46-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Bromo-3-methyl-1H-indazole

1.2 Other means of identification

Product number -
Other names -

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:90221-46-8 SDS

90221-46-8Relevant articles and documents

Preparation method of pazopanib intermediate

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Paragraph 0163-0165, (2021/03/24)

The invention provides a preparation method of a pazopanib key intermediate 2,3-dimethyl-N-(2-chloropyrimidin-4-yl)-N-methyl-2H-indazole-6-amine. The method comprises the following steps: by taking 6-halogenated-2,3-dimethyl-2H-indazole as a raw material, conducting reacting to obtain N,2,3-trimethyl-2H-indazole-6-amine; and further carrying out a reaction to obtain the 2,3-dimethyl-N-(2-chloropyrimidin-4-yl)-N-methyl-2H-indazole-6-amine. The method has the advantages of short synthesis route, accessible raw materials, low cost, mild reaction conditions, high safety and high yield, and is suitable for industrial mass production.

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