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1073372-08-3

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1073372-08-3 Usage

Description

4-(2-Cyanoethylaminocarbonyl)phenylboronic acid, propanediol cyclic ester is a complex chemical compound characterized by the presence of a boronic acid group, a propanediol cyclic ester moiety, and a cyanoethylamino carbonyl group. Its multifunctional structure suggests potential applications in pharmaceutical synthesis and organic chemistry, particularly due to its ability to participate in Suzuki-Miyaura cross-coupling reactions for carbon-carbon bond formation.

Uses

Used in Pharmaceutical Synthesis:
4-(2-Cyanoethylaminocarbonyl)phenylboronic acid, propanediol cyclic ester is used as a building block in the synthesis of larger, more complex molecules for pharmaceutical applications. Its unique combination of functional groups allows for versatile chemical reactions and the creation of novel therapeutic agents.
Used in Organic Synthesis:
In the field of organic synthesis, 4-(2-Cyanoethylaminocarbonyl)phenylboronic acid, propanediol cyclic ester is used as a reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool for forming carbon-carbon bonds, which is essential in constructing a wide range of organic compounds, including pharmaceuticals, agrochemicals, and materials.
Used in Medication Development:
4-(2-Cyanoethylaminocarbonyl)phenylboronic acid, propanediol cyclic ester's potential as a pharmaceutical precursor makes it valuable in the development of new medications. Its ability to be incorporated into larger molecules with specific biological activities can lead to the discovery of new drugs with improved efficacy and selectivity.
Used in Chemical Research:
4-(2-Cyanoethylaminocarbonyl)phenylboronic acid, propanediol cyclic ester serves as a subject of study in chemical research, where its unique properties and reactivity are explored. Understanding its behavior in various chemical reactions can contribute to the advancement of synthetic methodologies and the design of new chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1073372-08-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,7 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1073372-08:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*7)+(3*2)+(2*0)+(1*8)=133
133 % 10 = 3
So 1073372-08-3 is a valid CAS Registry Number.

1073372-08-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-Cyanoethyl)-4-(1,3,2-dioxaborinan-2-yl)benzamide

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

Emergency phone number -
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More Details:1073372-08-3 SDS

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