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(Ethene-1,2-diyldibenzene-2,1-diyl)diboronic acid is a complex chemical compound characterized by its molecular formula C14H16B2O4. It features two boronic acid groups and two benzene rings interconnected by an ethene-1,2-diyldibenzene-2,1-diyl bridge, which contributes to its unique molecular structure and properties.

7147-05-9

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7147-05-9 Usage

Uses

Used in Organic Chemistry:
(Ethene-1,2-diyldibenzene-2,1-diyl)diboronic acid is utilized as a reagent in organic chemistry for the synthesis of various organic molecules. Its boronic acid groups are significant due to their ability to form stable covalent bonds with cis-1,2-dihydroxy groups in diols, which is a key aspect of its application.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of organic chemistry, (ethene-1,2-diyldibenzene-2,1-diyl)diboronic acid is also used as a crucial component in Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed for the formation of carbon-carbon bonds, which are essential in the synthesis of complex organic compounds.
Used in Pharmaceutical Development:
The unique molecular structure and properties of (ethene-1,2-diyldibenzene-2,1-diyl)diboronic acid make it a valuable building block for the development of new pharmaceuticals. Its potential applications in this industry include the creation of novel drugs with specific targeting and therapeutic properties.
Used in Agrochemical Development:
Similarly, (ethene-1,2-diyldibenzene-2,1-diyl)diboronic acid is used in the development of new agrochemicals, where its unique structure can be leveraged to create compounds with enhanced efficacy and selectivity for pest control and crop protection.
Used in Material Science:
(ethene-1,2-diyldibenzene-2,1-diyl)diboronic acid's distinctive molecular structure also renders it useful in material science, where it can be employed as a building block for the development of new materials with specific properties, such as improved conductivity, strength, or chemical resistance.

Check Digit Verification of cas no

The CAS Registry Mumber 7147-05-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,4 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 7147-05:
(6*7)+(5*1)+(4*4)+(3*7)+(2*0)+(1*5)=89
89 % 10 = 9
So 7147-05-9 is a valid CAS Registry Number.

7147-05-9SDS

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 2,2'-Stilbenediboronic 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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7147-05-9 SDS

7147-05-9Upstream product

7147-05-9Downstream Products

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