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(4-CHLORO-2-CYANOPHENYL)BORONIC ACID is an organic compound that features a boronic acid group attached to a chloro-cyanophenyl moiety. (4-CHLORO-2-CYANOPHENYL)BORONIC ACID is characterized by its unique structure, which includes a chlorine atom at the 4-position and a nitrile group at the 2-position on a phenyl ring. Its chemical formula is C7H4BClNO2, and it has a molecular weight of approximately 188.38 g/mol. This versatile molecule is known for its reactivity and potential applications in various chemical and pharmaceutical processes.

819070-53-6

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819070-53-6 Usage

Uses

Used in Pharmaceutical Industry:
(4-CHLORO-2-CYANOPHENYL)BORONIC ACID is used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the production of 4-arylpiperidines. These 4-arylpiperidines are important structural motifs found in a variety of bioactive molecules, including antidepressants, antipsychotics, and other central nervous system (CNS) active drugs. The incorporation of the chloro-cyanophenyl moiety in these compounds can potentially enhance their pharmacological properties, such as potency, selectivity, and metabolic stability.
Used in Organic Synthesis:
In the field of organic synthesis, (4-CHLORO-2-CYANOPHENYL)BORONIC ACID serves as a valuable building block for the construction of complex organic molecules. Its reactivity allows it to participate in various chemical reactions, such as cross-coupling reactions, which can be used to form carbon-carbon or carbon-heteroatom bonds. This makes it a useful tool for the synthesis of a wide range of organic compounds, including natural products, pharmaceuticals, and functional materials.
Used in Material Science:
(4-CHLORO-2-CYANOPHENYL)BORONIC ACID can also be utilized in the development of new materials with unique properties. For instance, its incorporation into polymers or other macromolecular structures can lead to materials with improved mechanical, thermal, or electronic properties. Additionally, the presence of the boronic acid group may enable the formation of reversible covalent bonds with specific targets, such as sugars or nucleic acids, which could be useful in the design of responsive or adaptive materials.

Check Digit Verification of cas no

The CAS Registry Mumber 819070-53-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,9,0,7 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 819070-53:
(8*8)+(7*1)+(6*9)+(5*0)+(4*7)+(3*0)+(2*5)+(1*3)=166
166 % 10 = 6
So 819070-53-6 is a valid CAS Registry Number.

819070-53-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-chloro-2-cyanophenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 4-Chloro-2-cyanophenylboronic 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:819070-53-6 SDS

819070-53-6Relevant articles and documents

An efficient synthesis of a highly functionalized 4-arylpiperidine

Boice, Geneviève N.,Savarin, Cécile G.,Murry, Jerry A.,Conrad, Karen,Matty, Louis,Corley, Edward G.,Smitrovich, Jacqueline H.,Hughes, Dave

, p. 11367 - 11374 (2007/10/03)

In this manuscript, an efficient synthesis of a functionalized 4-arylpiperidine is disclosed. Several synthetic approaches towards formation of the key aryl-piperidine sp3 carbon-carbon bond are discussed, including a scalable route to the piperidine via

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