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352535-96-7

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352535-96-7 Usage

Description

2-FLUORO-5-(TRIFLUOROMETHYL)PHENYLBORONIC ACID is an organic compound that features a boronic acid structure with a fluorine atom at the 2nd position and a trifluoromethyl group at the 5th position on a phenyl ring. 2-FLUORO-5-(TRIFLUOROMETHYL)PHENYLBORONIC ACID is known for its chemical reactivity and is commonly used in various chemical reactions and synthesis processes.

Uses

Used in Suzuki Reaction:
2-FLUORO-5-(TRIFLUOROMETHYL)PHENYLBORONIC ACID is used as a reactant in the Suzuki reaction, a widely employed method for the formation of carbon-carbon bonds, particularly in the synthesis of biaryl compounds. Its unique structure allows for the formation of new bonds with other organic molecules, contributing to the diversity of chemical products.
Used in Organic Synthesis:
2-FLUORO-5-(TRIFLUOROMETHYL)PHENYLBORONIC ACID is used as a reactant for functionalization via lithiation and reaction with electrophiles. This process enables the introduction of various functional groups to the molecule, expanding its potential applications in the synthesis of complex organic compounds.
Used in Pharmaceutical Industry:
2-FLUORO-5-(TRIFLUOROMETHYL)PHENYLBORONIC ACID is used as a reactant in the preparation of inhibitors of kinesin spindle protein (KSP) for potential use as antitumor agents. Its unique structure and reactivity make it a valuable component in the development of new drugs targeting cancer cells.
Used in Chemical Research:
2-FLUORO-5-(TRIFLUOROMETHYL)PHENYLBORONIC ACID is used as a reactant in selective rhodium-catalyzed conjugate addition reactions. This application is particularly relevant in the field of chemical research, where the compound's unique properties can be exploited to develop new synthetic routes and methodologies.
Chemical Properties:
2-FLUORO-5-(TRIFLUOROMETHYL)PHENYLBORONIC ACID is an off-white crystalline solid, which indicates its solid-state structure and appearance.

Check Digit Verification of cas no

The CAS Registry Mumber 352535-96-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,2,5,3 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 352535-96:
(8*3)+(7*5)+(6*2)+(5*5)+(4*3)+(3*5)+(2*9)+(1*6)=147
147 % 10 = 7
So 352535-96-7 is a valid CAS Registry Number.
InChI:InChI=1/C7H5BF4O2/c9-6-2-1-4(7(10,11)12)3-5(6)8(13)14/h1-3,13-14H

352535-96-7 Well-known Company Product Price

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  • TCI America

  • (F0788)  2-Fluoro-5-(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)  

  • 352535-96-7

  • 1g

  • 390.00CNY

  • Detail
  • TCI America

  • (F0788)  2-Fluoro-5-(trifluoromethyl)phenylboronic Acid (contains varying amounts of Anhydride)  

  • 352535-96-7

  • 5g

  • 1,240.00CNY

  • Detail

352535-96-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-fluoro-5-(trifluoromethyl)phenyl]boronic acid

1.2 Other means of identification

Product number -
Other names 2-Fluoro-5-(trifluoromethyl)phenylboroni

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:352535-96-7 SDS

352535-96-7Relevant articles and documents

PROCESS FOR PRODUCING ORGANOLITHIUM COMPOUND AND PROCESS FOR PRODUCING SUBSTITUTED AROMATIC COMPOUND

-

, (2011/10/04)

A method for producing an organolithium compound includes the step of reacting an aromatic compound or a halogenated unsaturated aliphatic compound and a lithiating agent in the presence of a coordinating compound containing three or more elements having a coordinating ability in a molecule, at least one thereof being a nitrogen element, or a coordinating compound containing three or more oxygen elements having a coordinating ability in a molecule, at least one of the groups containing the oxygen elements having a coordinating ability being a tertiary alkoxy group, at a temperature of ?40° C. to 40° C.

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