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5-Borono-4-chloro-2-methoxybenzoic acid is a chemical compound characterized by the presence of a boronic acid group, a chloro substituent, and a methoxy group attached to a benzoic acid backbone. 5-Borono-4-chloro-2-methoxybenzoic acid is known for its unique reactivity in chemical reactions due to the boronic acid group, which is instrumental in forming carbon-carbon bonds. The chloro and methoxy substituents further contribute to the compound's structural and property profile, potentially affecting its solubility, stability, and biological activity. It is a versatile and significant compound with a wide range of applications in the fields of organic synthesis, medicinal chemistry, and beyond.

957066-09-0

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957066-09-0 Usage

Uses

Used in Organic Synthesis:
5-Borono-4-chloro-2-methoxybenzoic acid is utilized as a key building block in organic synthesis for the creation of pharmaceuticals and agrochemicals. Its boronic acid group provides unique reactivity, facilitating the formation of carbon-carbon bonds, which is crucial for the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-Borono-4-chloro-2-methoxybenzoic acid serves as an important intermediate for the development of new drugs. Its structural features, including the chloro and methoxy groups, can be tailored to enhance the compound's biological activity and selectivity towards specific targets, thereby contributing to the discovery of novel therapeutic agents.
Used in Chemical Research:
5-Borono-4-chloro-2-methoxybenzoic acid is also employed in chemical research to explore new reaction pathways and mechanisms. Its unique reactivity and structural attributes make it an attractive candidate for studying the fundamental aspects of chemical bonding and reaction dynamics.
Used in the Agrochemical Industry:
5-Borono-4-chloro-2-methoxybenzoic acid is used as a precursor in the synthesis of agrochemicals, such as pesticides and herbicides. Its potential to be modified and functionalized allows for the development of compounds with improved efficacy and selectivity in agricultural applications.
Used in the Development of Advanced Materials:
5-Borono-4-chloro-2-methoxybenzoic acid's unique structure and properties also make it a candidate for the development of advanced materials with specific applications in various industries, such as electronics, coatings, and polymers. Its potential to form stable and functional materials can contribute to the advancement of technology and innovation in material science.

Check Digit Verification of cas no

The CAS Registry Mumber 957066-09-0 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, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 957066-09:
(8*9)+(7*5)+(6*7)+(5*0)+(4*6)+(3*6)+(2*0)+(1*9)=200
200 % 10 = 0
So 957066-09-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H8BClO5/c1-15-7-3-6(10)5(9(13)14)2-4(7)8(11)12/h2-3,13-14H,1H3,(H,11,12)

957066-09-0SDS

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 5-Borono-4-chloro-2-methoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 5-Carboxy-2-chloro-4-methoxyphenylboronic 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:957066-09-0 SDS

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