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Boronic acid, B-[3-[(propylamino)carbonyl]phenyl]-, also known as 3-(propylcarbamoyl)phenylboronic acid, is a chemical compound with the molecular formula C12H16BNO3. It belongs to the class of organic compounds known as phenylboronic acids, which are used in synthetic organic chemistry as reagents for the selective formation of C-C bonds. This particular boronic acid is characterized by its unique structure that includes a phenyl group, a propylcarbamoyl group, and a boronic acid moiety. It is a versatile and important compound with a wide range of applications in the field of organic chemistry and drug discovery.

850567-22-5

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850567-22-5 Usage

Uses

Used in Pharmaceutical Synthesis:
Boronic acid, B-[3-[(propylamino)carbonyl]phenyl]is used as a reagent in the synthesis of potential drugs and pharmaceuticals. Its ability to selectively form C-C bonds makes it a valuable tool in the development of new and innovative medications.
Used in Material Science:
In the field of material science, Boronic acid, B-[3-[(propylamino)carbonyl]phenyl]is used in the development of new materials and technologies. Its unique chemical properties allow it to be incorporated into various materials, enhancing their performance and functionality.
Used in Medical Imaging:
Boronic acid, B-[3-[(propylamino)carbonyl]phenyl]has been studied for its potential use in medical imaging. Its ability to selectively bind to certain biological targets makes it a promising candidate for the development of imaging agents that can provide detailed insights into the structure and function of biological systems.
Used in Cancer Therapy:
In the field of cancer therapy, Boronic acid, B-[3-[(propylamino)carbonyl]phenyl]has been investigated for its potential use in the treatment of various types of cancer. Its unique chemical properties may allow it to selectively target cancer cells, leading to the development of more effective and targeted cancer therapies.
Used in Organic Chemistry Research:
Boronic acid, B-[3-[(propylamino)carbonyl]phenyl]is also used in organic chemistry research to explore new synthetic pathways and develop innovative chemical reactions. Its unique structure and reactivity make it an important compound for advancing the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 850567-22-5 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, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 850567-22:
(8*8)+(7*5)+(6*0)+(5*5)+(4*6)+(3*7)+(2*2)+(1*2)=175
175 % 10 = 5
So 850567-22-5 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BNO3/c1-2-6-12-10(13)8-4-3-5-9(7-8)11(14)15/h3-5,7,14-15H,2,6H2,1H3,(H,12,13)

850567-22-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H53344)  3-(n-Propylcarbamoyl)benzeneboronic acid, 95%   

  • 850567-22-5

  • 250mg

  • 599.0CNY

  • Detail
  • Alfa Aesar

  • (H53344)  3-(n-Propylcarbamoyl)benzeneboronic acid, 95%   

  • 850567-22-5

  • 1g

  • 1917.0CNY

  • Detail

850567-22-5SDS

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-(N-Propylaminocarbonyl)phenylboronic acid

1.2 Other means of identification

Product number -
Other names [3-(propylcarbamoyl)phenyl]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:850567-22-5 SDS

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