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2-Bromo-3-ethoxy-6-fluorophenylboronic acid is a boronic acid derivative characterized by the presence of bromine, ethoxy, and fluorine substituents on its phenyl ring. 2-BROMO-3-ETHOXY-6-FLUOROPHENYLBORONIC& is recognized for its role as a building block in organic synthesis, facilitating the creation of more intricate organic molecules. The inherent ability of boronic acids to form stable complexes with diols and their utility in Suzuki coupling reactions for carbon-carbon bond formation are notable features of this chemical. Its potential applications extend to the pharmaceutical industry, where boronic acids contribute to the development of drugs and pharmaceutical intermediates. The presence of a fluorine atom on the phenyl ring may also engender specific properties valuable in medicinal chemistry and material science.

849052-19-3

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849052-19-3 Usage

Uses

Used in Organic Synthesis:
2-Bromo-3-ethoxy-6-fluorophenylboronic acid is utilized as a building block in organic synthesis for constructing complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of various organic compounds.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-Bromo-3-ethoxy-6-fluorophenylboronic acid is used as a precursor in the development of drugs and pharmaceutical intermediates. The incorporation of boronic acid structures can enhance the pharmacological properties of drug candidates, potentially leading to improved therapeutic agents.
Used in Medicinal Chemistry:
2-Bromo-3-ethoxy-6-fluorophenylboronic acid is employed in medicinal chemistry to explore the effects of the fluorine substituent on the phenyl ring. The presence of fluorine can influence the molecule's lipophilicity, metabolic stability, and binding affinity, which are critical factors in drug design and optimization.
Used in Material Science:
In material science, 2-Bromo-3-ethoxy-6-fluorophenylboronic acid may be used to investigate the impact of its structural features on material properties. The integration of such molecules into materials could lead to advancements in areas such as polymer chemistry, where their unique interactions with other molecules could be harnessed for specific applications.

Check Digit Verification of cas no

The CAS Registry Mumber 849052-19-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,0,5 and 2 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849052-19:
(8*8)+(7*4)+(6*9)+(5*0)+(4*5)+(3*2)+(2*1)+(1*9)=183
183 % 10 = 3
So 849052-19-3 is a valid CAS Registry Number.
InChI:InChI=1S/C8H9BBrFO3/c1-2-14-6-4-3-5(11)7(8(6)10)9(12)13/h3-4,12-13H,2H2,1H3

849052-19-3SDS

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-Bromo-3-ethoxy-6-fluorophenyl)boronic acid

1.2 Other means of identification

Product number -
Other names (2-bromo-3-ethoxy-6-fluorophenyl)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:849052-19-3 SDS

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