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2-Bromo-3,6-difluorophenylboronic acid, with the molecular formula C6H4BBrF2O2, is a boronic acid derivative that is widely utilized in the fields of organic synthesis and medicinal chemistry. This chemical compound is characterized by its high reactivity and versatility, which makes it an indispensable building block for the creation of biologically active molecules and pharmaceuticals. The presence of a boronic acid group in its structure facilitates the formation of stable and selective covalent bonds with other organic molecules, thereby enhancing its utility in drug development and the synthesis of bioactive compounds. Furthermore, the incorporation of fluorine and bromine substituents endows 2-broMo-3,6-difluorophenylboronic acid with unique chemical properties that can be strategically employed in diverse synthetic applications.

1260757-41-2

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1260757-41-2 Usage

Uses

Used in Pharmaceutical Industry:
2-Bromo-3,6-difluorophenylboronic acid serves as a key intermediate in the synthesis of pharmaceuticals due to its ability to form stable covalent bonds with other organic molecules. Its unique chemical properties, conferred by the presence of fluorine and bromine substituents, make it a valuable asset in the development of new drugs with improved pharmacological profiles.
Used in Organic Synthesis:
In the realm of organic synthesis, 2-bromo-3,6-difluorophenylboronic acid is employed as a versatile building block for the construction of complex organic molecules. Its reactivity and the presence of the boronic acid group allow for a wide range of synthetic transformations, enabling the synthesis of diverse biologically active compounds and advanced materials.
Used in Medicinal Chemistry:
2-Bromo-3,6-difluorophenylboronic acid is utilized as a synthetic precursor in medicinal chemistry for the design and synthesis of novel bioactive molecules. Its unique structural features and reactivity enable the development of compounds with potential therapeutic applications, contributing to the discovery of new drugs and therapeutic agents.
Used in Chemical Research:
In the field of chemical research, 2-bromo-3,6-difluorophenylboronic acid is employed as a model compound to study various reaction mechanisms and explore new synthetic methodologies. Its unique properties and reactivity provide valuable insights into the fundamental aspects of organic and organometallic chemistry, paving the way for the development of innovative synthetic strategies and techniques.

Check Digit Verification of cas no

The CAS Registry Mumber 1260757-41-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,7,5 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1260757-41:
(9*1)+(8*2)+(7*6)+(6*0)+(5*7)+(4*5)+(3*7)+(2*4)+(1*1)=152
152 % 10 = 2
So 1260757-41-2 is a valid CAS Registry Number.

1260757-41-2SDS

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-3,6-difluorophenyl)boronic acid

1.2 Other means of identification

Product number -
Other names 2-bromo-3,6-difluorophenylboronic 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 -
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More Details:1260757-41-2 SDS

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