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5-Fluoro-2-(4-fluorophenylmethoxy)phenylboronic acid is a chemical compound that features a boronic acid group connected to a phenyl ring, which is adorned with fluorine and methoxy substituents. 5-Fluoro-2-(4-fluorophenylmethoxy)phenylboronic acid is characterized by a molecular formula of C13H10BFO3 and possesses a molar mass of 244.03 g/mol. It is recognized for its utility in organic synthesis, where it serves as a key building block in the creation of pharmaceuticals, agrochemicals, and other materials. The boronic acid functionality within this molecule is especially notable for its role in cross-coupling reactions with organic halides, establishing it as a versatile and significant reagent in organic chemistry.

1256355-74-4

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1256355-74-4 Usage

Uses

Used in Organic Synthesis:
5-Fluoro-2-(4-fluorophenylmethoxy)phenylboronic acid is used as a reagent for the synthesis of complex organic molecules, particularly in the pharmaceutical and agrochemical industries. Its boronic acid group facilitates cross-coupling reactions with organic halides, allowing for the formation of new carbon-carbon bonds, which are crucial for the construction of a wide range of chemical structures.
Used in Pharmaceutical Development:
In the pharmaceutical industry, 5-Fluoro-2-(4-fluorophenylmethoxy)phenylboronic acid is employed as a building block for the preparation of various drugs. Its unique structure and reactivity enable the creation of new compounds with potential therapeutic applications, contributing to the development of novel medications.
Used in Agrochemical Production:
5-Fluoro-2-(4-fluorophenylmethoxy)phenylboronic acid is also utilized in the agrochemical sector, where it serves as a key component in the synthesis of new pesticides and other agricultural chemicals. Its role in cross-coupling reactions allows for the design of innovative compounds that can improve crop protection and yield.
Used in Material Science:
In the field of material science, 5-Fluoro-2-(4-fluorophenylmethoxy)phenylboronic acid is used as a precursor for the development of new materials with specific properties. Its incorporation into the molecular structure of these materials can lead to enhanced performance characteristics, such as improved strength, durability, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 1256355-74-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,5 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1256355-74:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*5)+(3*5)+(2*7)+(1*4)=164
164 % 10 = 4
So 1256355-74-4 is a valid CAS Registry Number.

1256355-74-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [5-fluoro-2-[(4-fluorophenyl)methoxy]phenyl]boronic acid

1.2 Other means of identification

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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

1.5 Emergency phone number

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More Details:1256355-74-4 SDS

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