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4-(Phenethylcarbamoyl)phenylboronic acid is a boronic acid derivative characterized by the attachment of a phenethylcarbamoyl group to the phenyl ring. This chemical compound is part of the phenylboronic acids class and has garnered interest due to its potential applications in pharmaceutical development and organic synthesis. The unique properties conferred by the phenethylcarbamoyl group, along with the reversible covalent bonding ability of boronic acids with certain biomolecules, position 4-(Phenethylcarbamoyl)phenylboronic acid as a promising candidate for drug discovery and other specialized uses.

330793-46-9

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330793-46-9 Usage

Uses

Used in Pharmaceutical Development:
4-(Phenethylcarbamoyl)phenylboronic acid serves as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for specific interactions with biological targets, making it a valuable component in the design of new drugs with potential therapeutic effects.
Used in Organic Synthesis:
As a boronic acid derivative, 4-(Phenethylcarbamoyl)phenylboronic acid is utilized in organic synthesis for the formation of carbon-carbon bonds, a fundamental aspect of creating complex organic molecules. Its reactivity and selectivity in various coupling reactions contribute to the synthesis of a wide range of organic compounds.
Used in Medicinal Chemistry:
4-(Phenethylcarbamoyl)phenylboronic acid is employed in medicinal chemistry for its ability to form reversible covalent bonds with biomolecules. This feature is particularly useful in the development of probes and inhibitors that can modulate biological processes at the molecular level, offering insights into disease mechanisms and potential therapeutic interventions.
Used in Chemical Biology:
In the field of chemical biology, 4-(Phenethylcarbamoyl)phenylboronic acid is used as a tool to study the interactions between small molecules and biological systems. Its specific properties allow researchers to investigate the mechanisms of action of potential drugs and to understand the molecular basis of various biological processes.

Check Digit Verification of cas no

The CAS Registry Mumber 330793-46-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,0,7,9 and 3 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 330793-46:
(8*3)+(7*3)+(6*0)+(5*7)+(4*9)+(3*3)+(2*4)+(1*6)=139
139 % 10 = 9
So 330793-46-9 is a valid CAS Registry Number.

330793-46-9 Well-known Company Product Price

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  • Alfa Aesar

  • (H52991)  4-(2-Phenylethylcarbamoyl)benzeneboronic acid, 98%   

  • 330793-46-9

  • 250mg

  • 552.0CNY

  • Detail
  • Alfa Aesar

  • (H52991)  4-(2-Phenylethylcarbamoyl)benzeneboronic acid, 98%   

  • 330793-46-9

  • 1g

  • 1764.0CNY

  • Detail

330793-46-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(Phenethylcarbamoyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names 4-(2-Phenylethylcarbamoyl)benzeneboronic 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:330793-46-9 SDS

330793-46-9Downstream Products

330793-46-9Relevant academic research and scientific papers

Pyrazolopyrimidines as therapeutic agents

-

, (2008/06/13)

The present invention is directed to pyrazolopyrimidine derivatives of formula (I) wherein the substituents are defined herein, which are useful as kinase inhibitors and as such are useful for affecting angiogenesis and diseases and conditions associated with angiogenesis.

Pyrazolopyrimidines as therapeutic agents

-

, (2008/06/13)

The present invention provides compounds of Formula I, including pharmaceutically acceptable salts and/or prodrugs thereof, where G, R2, and R3 are defined as described herein.

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