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6-Chloro-1-methyl-1H-indol-2-ylboronic acid is a chemical compound with the molecular formula C9H9BClNO2. It is a versatile building block in organic synthesis and medicinal chemistry, characterized by the presence of a boronic acid group and an indole moiety. This unique structure makes it a valuable tool for the formation of carbon-carbon bonds through Suzuki-Miyaura coupling reactions and a promising intermediate for the synthesis of pharmaceuticals and agrochemicals. Its potential biological activity also makes it a subject of interest for drug discovery and development.

957066-11-4

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957066-11-4 Usage

Uses

Used in Organic Synthesis:
6-Chloro-1-methyl-1H-indol-2-ylboronic acid is used as a building block in organic synthesis for the creation of more complex compounds. Its boronic acid group facilitates the formation of carbon-carbon bonds through Suzuki-Miyaura coupling reactions, making it a valuable tool in the synthesis of various organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 6-Chloro-1-methyl-1H-indol-2-ylboronic acid is used as a versatile intermediate for the synthesis of pharmaceuticals. Its unique structure allows for the development of new drug candidates with potential therapeutic applications.
Used in Drug Discovery and Development:
The indole moiety present in 6-Chloro-1-methyl-1H-indol-2-ylboronic acid gives it potential biological activity, making it a subject of interest for drug discovery and development. Researchers can explore its properties and interactions with biological targets to identify new therapeutic agents.
Used in Agrochemical Synthesis:
6-Chloro-1-methyl-1H-indol-2-ylboronic acid is also used in the synthesis of agrochemicals, where its unique structure and reactivity can contribute to the development of new pesticides, herbicides, or other agricultural chemicals.
Overall, 6-Chloro-1-methyl-1H-indol-2-ylboronic acid is a valuable and versatile chemical tool with a wide range of applications in the fields of organic chemistry, medicinal research, drug discovery, and agrochemical development.

Check Digit Verification of cas no

The CAS Registry Mumber 957066-11-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,7,0,6 and 6 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 957066-11:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*6)+(2*1)+(1*1)=194
194 % 10 = 4
So 957066-11-4 is a valid CAS Registry Number.
InChI:InChI=1/C9H9BClNO2/c1-12-8-5-7(11)3-2-6(8)4-9(12)10(13)14/h2-5,13-14H,1H3

957066-11-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-Chloro-1-methylindole-2-boronic acid

1.2 Other means of identification

Product number -
Other names (6-chloro-1-methylindol-2-yl)boronic 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:957066-11-4 SDS

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