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3-(Ethyl(methyl)carbamoyl)phenylboronic acid is a boronic acid derivative with the molecular formula C10H15BClNO3. It is characterized by the presence of a boron atom bonded to a phenyl group and a carbamoyl group, which endows it with unique reactivity in chemical reactions. 3-(ETHYL(METHYL)CARBAMOYL)PHENYLBORONIC ACID is widely recognized for its utility in organic synthesis, particularly as a reagent in coupling reactions and as a building block in the synthesis of pharmaceutical compounds. Its ability to participate in Suzuki-Miyaura coupling reactions makes it a valuable component in the production of biaryl compounds, a class of molecules with significant applications in medicinal chemistry and drug discovery.

871333-07-2

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871333-07-2 Usage

Uses

Used in Organic Synthesis:
3-(Ethyl(methyl)carbamoyl)phenylboronic acid is used as a reagent in coupling reactions for the formation of carbon-carbon bonds, which are crucial in the synthesis of complex organic molecules. Its participation in these reactions facilitates the creation of new chemical entities with potential applications in various fields.
Used in Pharmaceutical Compounds:
In the pharmaceutical industry, 3-(Ethyl(methyl)carbamoyl)phenylboronic acid serves as a key building block in the preparation of various medicinal compounds. Its structural features allow for the development of new drugs with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Medicinal Chemistry and Drug Discovery:
3-(Ethyl(methyl)carbamoyl)phenylboronic acid is utilized as a versatile component in the field of medicinal chemistry, where it contributes to the design and synthesis of novel bioactive molecules. Its potential as a building block in drug discovery makes it a valuable asset in the development of new therapeutic agents for the treatment of various diseases and conditions.
Used in the Production of Biaryl Compounds:
3-(Ethyl(methyl)carbamoyl)phenylboronic acid is employed in the synthesis of biaryl compounds through Suzuki-Miyaura coupling reactions. These biaryl compounds are important structural motifs in many pharmaceuticals and agrochemicals, making this boronic acid derivative an essential tool in the production of these valuable molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 871333-07-2 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 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 871333-07:
(8*8)+(7*7)+(6*1)+(5*3)+(4*3)+(3*3)+(2*0)+(1*7)=162
162 % 10 = 2
So 871333-07-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14BNO3/c1-3-12(2)10(13)8-5-4-6-9(7-8)11(14)15/h4-7,14-15H,3H2,1-2H3

871333-07-2 Well-known Company Product Price

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  • Alfa Aesar

  • (H52530)  3-[Ethyl(methyl)carbamoyl]benzeneboronic acid, 98%   

  • 871333-07-2

  • 250mg

  • 733.0CNY

  • Detail
  • Alfa Aesar

  • (H52530)  3-[Ethyl(methyl)carbamoyl]benzeneboronic acid, 98%   

  • 871333-07-2

  • 1g

  • 2346.0CNY

  • Detail

871333-07-2SDS

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-(Ethyl(methyl)carbamoyl)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [3-[ethyl(methyl)carbamoyl]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 -
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More Details:871333-07-2 SDS

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