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2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a boronic ester with the molecular formula C14H18BFO2Br. It features a fluorine atom and a bromomethyl group attached to a phenyl ring, along with a dioxaborolane moiety. This unique molecular structure endows it with distinctive reactivity and selectivity in chemical reactions, making it a valuable building block in organic synthesis for the creation of a wide range of organic molecules.

1029439-49-3

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1029439-49-3 Usage

Uses

Used in Pharmaceutical Development:
2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a key intermediate in the synthesis of pharmaceuticals for its ability to facilitate the formation of complex molecular structures. Its unique reactivity allows for the development of new drugs with specific therapeutic targets.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is utilized as a building block for the creation of novel agrochemicals, contributing to the development of more effective and targeted pesticides and herbicides.
Used in Materials Science:
2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is employed as a component in the synthesis of advanced materials, leveraging its unique properties to enhance material performance in various applications, such as in polymers and composites.
Used in Organic Chemistry Research:
As a versatile compound in organic chemistry, 2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used in research to explore new reaction pathways and mechanisms, contributing to the broader understanding of organic synthesis and the discovery of new chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 1029439-49-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,9,4,3 and 9 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1029439-49:
(9*1)+(8*0)+(7*2)+(6*9)+(5*4)+(4*3)+(3*9)+(2*4)+(1*9)=153
153 % 10 = 3
So 1029439-49-3 is a valid CAS Registry Number.

1029439-49-3 Well-known Company Product Price

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  • Alfa Aesar

  • (H59821)  4-Bromomethyl-2-fluorobenzeneboronic acid pinacol ester, 96%   

  • 1029439-49-3

  • 250mg

  • 914.0CNY

  • Detail
  • Alfa Aesar

  • (H59821)  4-Bromomethyl-2-fluorobenzeneboronic acid pinacol ester, 96%   

  • 1029439-49-3

  • 1g

  • 2925.0CNY

  • Detail

1029439-49-3SDS

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 2-(4-(Bromomethyl)-2-fluorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

1.2 Other means of identification

Product number -
Other names 2-[4-(bromomethyl)-2-fluorophenyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

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:1029439-49-3 SDS

1029439-49-3Relevant academic research and scientific papers

SUBSTITUTED BENZAZINONES AS ANTIBACTERIAL COMPOUNDS

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Page/Page column 195-196, (2017/07/14)

The present invention relates to LpxC antibacterial compounds of Formula (1A), corresponding pharmaceutically acceptable salts thereof, corresponding pharmaceutical compositions:, compound preparation, treatment methods and uses for bacterial infections, especially those caused by gram-negative bacteria.

DETECTION OF HYDROGEN PEROXIDE

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Paragraph 0086; 0096, (2013/03/26)

The present invention provides compounds of formula (I), (II) or (III) wherein R1and R11are boronic acid or a borate ester useful for detection of hydrogen peroxide and methods of using same.

INHIBITORS OF FATTY ACID AMIDE HYDROLASE

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Page/Page column 213, (2008/12/05)

The present invention provide compounds, and pharmaceutical compositions thereof, encompassed by the formulae (I), (II) or (III). The present invention also provides methods for treating FAAH mediated disease, disorder or condition by administering a ther

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