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3-Borono-5-methoxybenzoic acid is a boronic acid derivative with the molecular formula C8H9BO5 and a molar mass of 195.97 g/mol. It features a boron atom and a carboxylic acid group attached to a benzene ring, with a methoxy group at the 5-position. This chemical compound is known for its versatility in organic synthesis and its potential applications in various fields.

1050424-08-2

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1050424-08-2 Usage

Uses

Used in Organic Synthesis:
3-Borono-5-methoxybenzoic acid is used as a versatile building block in the synthesis of pharmaceuticals, agrochemicals, and other functional materials. Its unique structure allows for the formation of various chemical bonds and reactions, making it a valuable component in the creation of complex organic molecules.
Used in Cross-linking Applications:
As a cross-linking agent, 3-Borono-5-methoxybenzoic acid is utilized to form covalent bonds between different molecules, enhancing the stability and properties of the resulting compounds. This application is particularly useful in the development of polymers and materials with improved mechanical strength and chemical resistance.
Used in Complex Formation:
3-Borono-5-methoxybenzoic acid has the ability to form complexes with various other compounds, which can be beneficial in various chemical and biological processes. The formation of these complexes can lead to enhanced reactivity, selectivity, or stability, making it a valuable tool in research and development.
Used in Pharmaceutical Industry:
3-Borono-5-methoxybenzoic acid is studied for its potential as an anti-cancer agent, with research focusing on its ability to inhibit the growth and proliferation of cancer cells. Its biological activities also include inhibitory effects on specific enzymes, which can be harnessed for the development of novel therapeutic agents.
Used in Enzyme Inhibition:
3-Borono-5-methoxybenzoic acid has demonstrated inhibitory effects on certain enzymes, making it a potential candidate for the development of enzyme-targeting drugs. By selectively inhibiting the activity of specific enzymes, 3-Borono-5-methoxybenzoic acid could be used to treat various diseases and disorders related to enzyme dysfunction.

Check Digit Verification of cas no

The CAS Registry Mumber 1050424-08-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,5,0,4,2 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1050424-08:
(9*1)+(8*0)+(7*5)+(6*0)+(5*4)+(4*2)+(3*4)+(2*0)+(1*8)=92
92 % 10 = 2
So 1050424-08-2 is a valid CAS Registry Number.

1050424-08-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-borono-5-methoxybenzoic acid

1.2 Other means of identification

Product number -
Other names 3-Carboxy-5-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:1050424-08-2 SDS

1050424-08-2Downstream Products

1050424-08-2Relevant articles and documents

One-pot generation of lithium (lithiophenyl)trialkoxyborates from substituted dihalobenzenes (Hal = Br, I) and their derivatization with electrophiles

Kurach, Pawel,Lulinski, Sergiusz,Serwatowski, Janusz

experimental part, p. 3171 - 3178 (2009/05/30)

The simple one-pot approach to synthetically useful phenyltrialkoxyborates bearing lithium at the phenyl ring has been developed starting with 1,3- and 1,4-diiodobenzene, as well as several activated dibromobenzenes and bromoiodobenzenes. The general sequence of transformations involves halogen-lithium exchange by using nBuLi and subsequent boronation with a trialkylborate. The resulting lithium (halophenyl) trialkoxyborates were then subjected to halogen-lithium exchange in situ with a second equivalent of nBuLi to give dianionic lithium (lithiophenyl)trialkoxyborates. Treatment with selected electrophiles afforded substituted arylboronic acids and/or their pinacol esters as final products in moderate-to-good yields. Wiley-VCH Verlag GmbH & Co. KGaA, 2008.

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