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3-(Cyclohexylcarbamoyl)-5-nitrophenylboronic acid is a boronic acid derivative characterized by the presence of a boronic acid group attached to a phenyl ring, which is substituted with a nitro group and a cyclohexylcarbamoyl group. This chemical compound is widely utilized in organic synthesis and medicinal chemistry for the synthesis of various compounds, making it a valuable reagent in these fields. Its potential as a pharmaceutical intermediate and its applications in the development of new drugs have been the subject of research, highlighting its significance in the pharmaceutical industry. Furthermore, it is recognized for its role in the Suzuki-Miyaura cross-coupling reaction, a widely used method for forming carbon-carbon bonds.

871332-85-3

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871332-85-3 Usage

Uses

Used in Organic Synthesis:
3-(Cyclohexylcarbamoyl)-5-nitrophenylboronic acid is used as a reagent in organic synthesis for the preparation of various compounds. Its unique structure allows for versatile reactions and the formation of diverse chemical entities, making it a valuable tool in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(Cyclohexylcarbamoyl)-5-nitrophenylboronic acid is employed as a reagent for the synthesis of pharmaceutical compounds. Its potential as a pharmaceutical intermediate has been studied, and it may contribute to the development of new drugs with improved therapeutic properties.
Used in Pharmaceutical Industry:
3-(Cyclohexylcarbamoyl)-5-nitrophenylboronic acid is used as a key intermediate in the pharmaceutical industry for the development of novel drugs. Its unique chemical properties and reactivity make it a promising candidate for the synthesis of bioactive molecules with potential therapeutic applications.
Used in Suzuki-Miyaura Cross-Coupling Reaction:
3-(Cyclohexylcarbamoyl)-5-nitrophenylboronic acid is utilized in the Suzuki-Miyaura cross-coupling reaction, a widely employed method for the formation of carbon-carbon bonds. This reaction is crucial in the synthesis of various organic compounds, including those with pharmaceutical relevance, and the use of this boronic acid derivative enhances the scope and efficiency of this process.

Check Digit Verification of cas no

The CAS Registry Mumber 871332-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,3,3 and 2 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 871332-85:
(8*8)+(7*7)+(6*1)+(5*3)+(4*3)+(3*2)+(2*8)+(1*5)=173
173 % 10 = 3
So 871332-85-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H17BN2O5/c17-13(15-11-4-2-1-3-5-11)9-6-10(14(18)19)8-12(7-9)16(20)21/h6-8,11,18-19H,1-5H2,(H,15,17)

871332-85-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H53176)  3-Cyclohexylcarbamoyl-5-nitrobenzeneboronic acid, 97%   

  • 871332-85-3

  • 250mg

  • 926.0CNY

  • Detail
  • Alfa Aesar

  • (H53176)  3-Cyclohexylcarbamoyl-5-nitrobenzeneboronic acid, 97%   

  • 871332-85-3

  • 1g

  • 2964.0CNY

  • Detail

871332-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [3-(cyclohexylcarbamoyl)-5-nitrophenyl]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

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More Details:871332-85-3 SDS

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