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4-(4-Fluorophenyl)phenylboronic acid is a chemical compound that serves as a versatile reactant in the synthesis of various organic substances. It is characterized by a unique substitution pattern, featuring a fluorine atom attached to the phenyl ring, which can influence its reactivity and properties. 4-(4-Fluorophenyl)phenylboronic acid is also recognized for its stability under specific conditions, making it a valuable component in the creation of pharmaceutical drugs. The boronic acid component enables it to engage in chemical reactions with other compounds during the synthesis process, thereby broadening its applications in the field of chemistry, particularly in Suzuki coupling reactions.

140369-67-1

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140369-67-1 Usage

Uses

Used in Pharmaceutical Industry:
4-(4-Fluorophenyl)phenylboronic acid is used as a key reactant for the synthesis of pharmaceutical drugs, leveraging its stability and reactivity to create a wide range of medicinal compounds. Its unique substitution pattern with the fluorine atom can alter its properties, allowing for the development of new drug candidates with potentially improved therapeutic effects.
Used in Organic Synthesis:
In the field of organic chemistry, 4-(4-Fluorophenyl)phenylboronic acid is employed as a reactant in the preparation of various organic substances. Its boronic acid component facilitates chemical reactions with other compounds, making it a valuable building block for the synthesis of complex organic molecules.
Used in Suzuki Coupling Reactions:
4-(4-Fluorophenyl)phenylboronic acid is utilized as a reagent in Suzuki coupling reactions, a type of cross-coupling reaction that forms carbon-carbon bonds. Its unique substitution pattern and reactivity make it a preferred choice for this process, contributing to the synthesis of a variety of organic compounds with potential applications in various industries.
Safety and Handling:
Due to its potential hazards, safety and handling measures must be taken into account when working with 4-(4-Fluorophenyl)phenylboronic acid. Proper precautions should be implemented to ensure the safety of researchers and the environment during its synthesis and use in various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 140369-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,3,6 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 140369-67:
(8*1)+(7*4)+(6*0)+(5*3)+(4*6)+(3*9)+(2*6)+(1*7)=121
121 % 10 = 1
So 140369-67-1 is a valid CAS Registry Number.
InChI:InChI=1/C12H10BFO2/c14-12-7-3-10(4-8-12)9-1-5-11(6-2-9)13(15)16/h1-8,15-16H

140369-67-1 Well-known Company Product Price

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  • Alfa Aesar

  • (H64421)  4'-Fluorobiphenyl-4-boronic acid, 98%   

  • 140369-67-1

  • 250mg

  • 500.0CNY

  • Detail
  • Alfa Aesar

  • (H64421)  4'-Fluorobiphenyl-4-boronic acid, 98%   

  • 140369-67-1

  • 1g

  • 1333.0CNY

  • Detail
  • Alfa Aesar

  • (H64421)  4'-Fluorobiphenyl-4-boronic acid, 98%   

  • 140369-67-1

  • 5g

  • 4998.0CNY

  • Detail

140369-67-1SDS

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 4-(4-Fluorophenyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names 4'-Fluorobiphenyl-4-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:140369-67-1 SDS

140369-67-1Downstream Products

140369-67-1Relevant academic research and scientific papers

COMPOUNDS FOR THE TREATMENT OF ONCOVIRUS INDUCED CANCER AND METHODS OF USE THEREOF

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Page/Page column 125, (2020/10/21)

The pesent invention relates to compounds of formula (I) pharmaceutically-acceptable salts, hydrates, solvates, or stereoisomers thereof and their use for the prevention and treatment of oncovirus induced cancer in a subject.

INHIBITORS OF NOTCH SIGNALLING PATHWAY AND USE THEREOF IN TREATMENT OF CANCERS

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Page/Page column 156, (2020/10/21)

The present invention relates to new inhibitors of Notch signalling pathway and its use in the treatment and/or prevention of cancers.

1, 3, 5 - cyclohexanetriol - cis - or organic boronic acid-stable siloxy inositol complex and organic synthetic reaction using a reagent art

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Paragraph 0167; 0168; 0184, (2017/06/02)

PROBLEM TO BE SOLVED: To provide a stable ate-type complex of an organoboronic acid as a reagent for organic synthesis reaction; and manufacturing techniques thereof.SOLUTION: A stable ate-type complex of an organoboronic acid with scyllo-inositol or 1,3,5-cis-cyclohexanetriol comprises an anion represented by the specified general formula (I) or (II) as a constituent. In the formula, Rand Reach represent an alkyl group, alkenyl group, alkynyl group, aryl group, heterocyclic group or aralkyl group which may have substituents.

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