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4-(2-BROMOETHOXY)PHENYLBORONIC ACID is a boronic acid derivative with the molecular formula C8H10BBrO3. It is an organoboron compound characterized by a phenyl group attached to the boron atom and a bromoethoxy group attached to the phenyl ring. 4-(2-BROMOETHOXY)PHENYLBORONIC ACID is widely used in organic synthesis, particularly as a reagent for the Suzuki-Miyaura coupling reaction, which is a method for forming carbon-carbon bonds. Its versatility and applications in the synthesis of pharmaceuticals, agrochemicals, and materials make it a valuable tool in the field of organic chemistry.

913836-06-3

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913836-06-3 Usage

Uses

Used in Pharmaceutical Synthesis:
4-(2-BROMOETHOXY)PHENYLBORONIC ACID is used as a building block for the synthesis of various pharmaceuticals. Its unique structure allows for the formation of carbon-carbon bonds through the Suzuki-Miyaura coupling reaction, enabling the creation of complex molecular structures with potential therapeutic properties.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-(2-BROMOETHOXY)PHENYLBORONIC ACID is used as a key intermediate in the synthesis of various agrochemicals. Its ability to form carbon-carbon bonds through the Suzuki-Miyaura coupling reaction contributes to the development of new and effective compounds for crop protection and pest control.
Used in Material Synthesis:
4-(2-BROMOETHOXY)PHENYLBORONIC ACID is also utilized in the synthesis of advanced materials, such as polymers and composites. Its reactivity in the Suzuki-Miyaura coupling reaction allows for the creation of novel materials with improved properties, such as enhanced stability, durability, or specific functional groups.
Used in Organic Synthesis:
As a versatile reagent in organic synthesis, 4-(2-BROMOETHOXY)PHENYLBORONIC ACID is used for the formation of carbon-carbon bonds through the Suzuki-Miyaura coupling reaction. This reaction is widely employed in the synthesis of various organic compounds, including natural products, pharmaceuticals, agrochemicals, and other specialty chemicals, making it a valuable tool for chemists in the field of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 913836-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,8,3 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 913836-06:
(8*9)+(7*1)+(6*3)+(5*8)+(4*3)+(3*6)+(2*0)+(1*6)=173
173 % 10 = 3
So 913836-06-3 is a valid CAS Registry Number.
InChI:InChI=1/C8H10BBrO3/c10-5-6-13-8-3-1-7(2-4-8)9(11)12/h1-4,11-12H,5-6H2

913836-06-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H52939)  4-(2-Bromoethoxy)benzeneboronic acid, 95%   

  • 913836-06-3

  • 250mg

  • 662.0CNY

  • Detail
  • Alfa Aesar

  • (H52939)  4-(2-Bromoethoxy)benzeneboronic acid, 95%   

  • 913836-06-3

  • 1g

  • 2117.0CNY

  • Detail

913836-06-3SDS

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 (4-(2-Bromoethoxy)phenyl)boronic acid

1.2 Other means of identification

Product number -
Other names [4-(2-bromoethoxy)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:913836-06-3 SDS

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