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5-Fluoro-6-methoxypyridine-3-boronic acid is a chemical compound that is frequently used in the field of chemistry, particularly in organic synthesis. As a boronic acid derivative, it is part of a versatile class of compounds known for their ability to form carbon-carbon bonds. This specific compound is notable for its fluoro and methoxy substituents on the pyridine ring, which contribute to its utility in the synthesis of a wide range of chemical structures. It is commonly employed in Suzuki-Miyaura coupling reactions, a highly effective method for creating biaryl compounds. The unique properties of 5-Fluoro-6-methoxypyridine-3-boronic acid render it a valuable asset in the development of pharmaceuticals and other complex organic molecules.

856250-60-7

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856250-60-7 Usage

Uses

Used in Pharmaceutical Development:
5-Fluoro-6-methoxypyridine-3-boronic acid is used as a synthetic intermediate for the creation of various pharmaceutical compounds. Its ability to participate in carbon-carbon bond-forming reactions, such as the Suzuki-Miyaura coupling, allows for the construction of complex molecular structures that are essential in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, 5-Fluoro-6-methoxypyridine-3-boronic acid is used as a key building block for the synthesis of diverse chemical structures. Its reactivity in boronic acid reactions enables the formation of new carbon-carbon bonds, which is crucial for the assembly of complex organic molecules.
Used in Suzuki-Miyaura Coupling Reactions:
5-Fluoro-6-methoxypyridine-3-boronic acid is used as a coupling partner in Suzuki-Miyaura coupling reactions. This reaction is a powerful method for creating biaryl compounds, which are important structural motifs in many pharmaceuticals and organic materials. The presence of the fluoro and methoxy groups on the pyridine ring of this boronic acid compound enhances its reactivity and selectivity in these coupling processes.

Check Digit Verification of cas no

The CAS Registry Mumber 856250-60-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,6,2,5 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 856250-60:
(8*8)+(7*5)+(6*6)+(5*2)+(4*5)+(3*0)+(2*6)+(1*0)=177
177 % 10 = 7
So 856250-60-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H7BFNO3/c1-12-6-5(8)2-4(3-9-6)7(10)11/h2-3,10-11H,1H3

856250-60-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (5-Fluoro-6-methoxypyridin-3-yl)boronic acid

1.2 Other means of identification

Product number -
Other names (5-fluoro-6-methoxypyridin-3-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:856250-60-7 SDS

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