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4-Bromo-2-fluoro-5-methylphenylboronic acid is a boronic acid derivative with the molecular formula C7H7BBrFO2. It features a boron atom attached to a phenyl ring that is substituted with bromine, fluorine, and methyl groups. 4-Bromo-2-fluoro-5-methylphenylboronic acid is recognized for its stability as a white to off-white solid under normal conditions, which makes it a versatile building block in organic synthesis and medicinal chemistry for constructing complex molecules.

677777-57-0

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677777-57-0 Usage

Uses

Used in Organic Synthesis:
4-Bromo-2-fluoro-5-methylphenylboronic acid serves as a key building block in organic synthesis, facilitating the creation of more intricate molecular structures. Its unique substitution pattern allows for a wide range of applications in the synthesis of various organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 4-Bromo-2-fluoro-5-methylphenylboronic acid is utilized for the development of pharmaceuticals. Its structural features make it a valuable component in the design and synthesis of potential drug candidates.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
4-Bromo-2-fluoro-5-methylphenylboronic acid is a crucial reagent in Suzuki-Miyaura cross-coupling reactions, a widely used method in the synthesis of pharmaceuticals, agrochemicals, and materials. This reaction allows for the formation of carbon-carbon bonds, which are essential in the construction of complex organic molecules.
Used in the Synthesis of Pharmaceuticals:
4-Bromo-2-fluoro-5-methylphenylboronic acid is employed as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs with potential therapeutic applications.
Used in the Synthesis of Agrochemicals:
4-Bromo-2-fluoro-5-methylphenylboronic acid is also utilized in the agrochemical industry for the synthesis of pesticides and other agrochemical products, highlighting its importance in various chemical industries.
Used in the Synthesis of Materials:
This boronic acid derivative is further applied in the synthesis of various materials, including those used in high-tech applications, due to its ability to participate in cross-coupling reactions that yield novel materials with desired properties.

Check Digit Verification of cas no

The CAS Registry Mumber 677777-57-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,7,7,7 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 677777-57:
(8*6)+(7*7)+(6*7)+(5*7)+(4*7)+(3*7)+(2*5)+(1*7)=240
240 % 10 = 0
So 677777-57-0 is a valid CAS Registry Number.

677777-57-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-Bromo-2-fluoro-5-methylphenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-Bromo-2-fluoro-5-methylphenylboronic 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:677777-57-0 SDS

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