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Organic compounds containing an indazole ring (a five-membered ring consisting of a benzene ring fused to a pyrazole ring)

1010102-31-4

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1010102-31-4 Usage

Chemical family

Indazoles

Compound type

Ester of 3-chloro-4-nitro-1H-indazole-1-carboxylic acid

Derivation

Reaction between 3-chloro-4-nitro-1H-indazole-1-carboxylic acid and 1,1-dimethylethyl alcohol

Physical form

Yellow solid

Molecular weight

301.67 g/mol

Potential applications

Organic synthesis and pharmaceutical research

Unique properties

Derived from a reaction with a specific starting material (3-chloro-4-nitro-1H-indazole-1-carboxylic acid) and a specific alcohol (1,1-dimethylethyl alcohol), resulting in a compound with a unique structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1010102-31-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,0,1,0 and 2 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1010102-31:
(9*1)+(8*0)+(7*1)+(6*0)+(5*1)+(4*0)+(3*2)+(2*3)+(1*1)=34
34 % 10 = 4
So 1010102-31-4 is a valid CAS Registry Number.

1010102-31-4SDS

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 tert-butyl 3-chloro-4-nitro-1H-indazole-1-carboxylate

1.2 Other means of identification

Product number -
Other names 1H-INDAZOLE-1-CARBOXYLIC ACID,3-CHLORO-4-NITRO-,1,1-DIMETHYLETHYL ESTER

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:1010102-31-4 SDS

1010102-31-4Relevant academic research and scientific papers

RAF INHIBITOR COMPOUNDS AND METHODS OF USE THEREOF

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Page/Page column 22, (2010/04/23)

Compounds of Formulas (I), (IIA) and (IIIA) are useful for inhibiting Raf kinase and for treating disorders mediated thereby. Methods of using compounds of Formulas (I), (IIA) and (IIIA) and stereoisomers and pharmaceutically acceptable salts thereof, for in vitro, in situ, and in vivo diagnosis, prevention or treatment of such disorders in mammalian cells, or associated pathological conditions are disclosed.

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