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3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID is a chemical compound that features a boronic acid functional group attached to a phenyl ring, which is further substituted with an aminocarbonyl and a 4-fluorophenyl group. 3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID is known for its utility in organic synthesis, particularly in the Suzuki-Miyaura cross-coupling reaction for the formation of carbon-carbon bonds. Its unique structure, with the boronic acid moiety and the substituents, endows it with the ability to selectively bind to diols or other Lewis bases, which is advantageous in biological and environmental studies. 3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID's specific chemical and biological properties also make it a valuable building block in drug discovery and materials science.

850567-35-0

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850567-35-0 Usage

Uses

Used in Organic Synthesis:
3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID is used as a reagent in the Suzuki-Miyaura cross-coupling reaction for the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules.
Used in Pharmaceutical Preparation:
In the Pharmaceutical Industry, 3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID is used as a key intermediate in the preparation of various pharmaceuticals. Its unique structure allows for the development of new drugs with specific therapeutic properties.
Used in Agrochemical Development:
3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID is utilized as a building block in the creation of agrochemicals, contributing to the development of effective and targeted pesticides or other agricultural chemicals.
Used in Materials Science:
In the Materials Science field, 3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID is employed in the synthesis of new materials with tailored properties, such as improved conductivity, stability, or specific interactions with biological systems.
Used in Biological and Environmental Studies:
3-(4-FLUOROPHENYL)AMINOCARBONYLPHENYLBORONIC ACID is used as a selective binding agent for diols or other Lewis bases, making it a useful tool in studying biological interactions and environmental processes.

Check Digit Verification of cas no

The CAS Registry Mumber 850567-35-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,0,5,6 and 7 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 850567-35:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*7)+(2*3)+(1*5)=180
180 % 10 = 0
So 850567-35-0 is a valid CAS Registry Number.
InChI:InChI=1/C13H11BFNO3/c15-11-4-6-12(7-5-11)16-13(17)9-2-1-3-10(8-9)14(18)19/h1-8,18-19H,(H,16,17)

850567-35-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-[(4-fluorophenyl)carbamoyl]phenyl]boronic 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

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:850567-35-0 SDS

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