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885518-47-8

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885518-47-8 Usage

General Description

Methyl 4-bromo-6-(1H)-indazole-1-carboxylate is a chemical compound that belongs to the indazole class. It is characterized by the presence of a methyl group, a bromine atom, and a carboxylate group attached to a 6-membered ring of the indazole molecule. Methyl 4-bromo-6-(1H)-ind... has potential applications in the fields of organic synthesis and pharmaceutical research due to its unique structure and reactivity. Its properties and uses also make it an important intermediate in the production of various drugs and other organic compounds. Additionally, it may have biological activities and pharmacological effects that could make it valuable for further study and potential medical applications.

Check Digit Verification of cas no

The CAS Registry Mumber 885518-47-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,5,1 and 8 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 885518-47:
(8*8)+(7*8)+(6*5)+(5*5)+(4*1)+(3*8)+(2*4)+(1*7)=218
218 % 10 = 8
So 885518-47-8 is a valid CAS Registry Number.

885518-47-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 4-bromo-1H-indazole-6-carboxylate

1.2 Other means of identification

Product number -
Other names methyl 4-bromo-1H-indazole-6-carboxylate

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:885518-47-8 SDS

885518-47-8Relevant articles and documents

SELECTIVE INHIBITORS OF CLINICALLY IMPORTANT MUTANTS OF THE EGFR TYROSINE KINASE

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Page/Page column 150, (2019/01/21)

The present invention provides compounds of Formula (I) or a subgeneric structure or species thereof, or a pharmaceutically acceptable salt, ester, solvate, and/or prodrug thereof, and methods and compositions for treating or ameliorating abnormal cell pr

Synthesis of substituted 4-(1H-indol-6-yl)-1H-indazoles as potential PDK1 inhibitors

Brzozowski, Martin,O'Brien, Nathan J.,Wilson, David J.D.,Abbott, Belinda M.

, p. 318 - 326 (2014/01/06)

The development of a preparative route to a series of novel 4-(1H-indol-6-yl)-1H-indazole compounds as potential PDK1 inhibitors is described. The synthetic strategy centres on the late-stage Suzuki cross-coupling of N-unprotected indazole and indole frag

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