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2,3-Difluoro-4-(methoxycarbonyl)phenylboronic acid is a boronic acid derivative with the molecular formula C8H8BF2O4. It features a boron atom bonded to a phenyl ring, with two fluorine atoms and a methoxycarbonyl group attached to the ring. 2,3-Difluoro-4-(methoxycarbonyl)phenylboronic acid has potential applications in organic synthesis and medicinal chemistry, particularly in pharmaceutical development. Boronic acids, including 2,3-Difluoro-4-(methoxycarbonyl)phenylboronic acid, are known for their ability to form stable complexes with diols and are often utilized in Suzuki coupling reactions and other organic transformations. The presence of fluorine atoms and the methoxycarbonyl group in 2,3-Difluoro-4-(methoxycarbonyl)phenylboronic acid may confer specific chemical and pharmacological properties, making it a subject of interest for further research and development.

1402238-29-2

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1402238-29-2 Usage

Uses

Used in Organic Synthesis:
2,3-Difluoro-4-(methoxycarbonyl)phenylboronic acid is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure allows it to participate in a range of reactions, including Suzuki coupling, which is a widely used method for the formation of carbon-carbon bonds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,3-Difluoro-4-(methoxycarbonyl)phenylboronic acid is used as a building block for the development of pharmaceuticals. Its ability to form stable complexes with diols and its potential to be modified through organic transformations make it a valuable component in the synthesis of new drug candidates.
Used in Pharmaceutical Development:
2,3-Difluoro-4-(methoxycarbonyl)phenylboronic acid is used as a key component in the design and synthesis of new pharmaceuticals. The presence of fluorine atoms can influence the compound's lipophilicity, metabolic stability, and receptor binding, which are critical factors in drug discovery. The methoxycarbonyl group may also contribute to the compound's biological activity and pharmacokinetic properties.
Used in Research and Development:
This boronic acid derivative is used in research and development for exploring its potential applications and properties. Its unique structure and reactivity make it a promising candidate for the development of new chemical processes and for understanding its interactions with biological systems.

Check Digit Verification of cas no

The CAS Registry Mumber 1402238-29-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,2,2,3 and 8 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1402238-29:
(9*1)+(8*4)+(7*0)+(6*2)+(5*2)+(4*3)+(3*8)+(2*2)+(1*9)=112
112 % 10 = 2
So 1402238-29-2 is a valid CAS Registry Number.

1402238-29-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-difluoro-4-(methoxycarbonyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names -

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

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More Details:1402238-29-2 SDS

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