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166281-37-4

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166281-37-4 Usage

Description

2-Bromo-4,5-difluorophenol is an organic compound characterized by the presence of a bromine atom at the 2nd position and two fluorine atoms at the 4th and 5th positions on a phenol molecule. It is known for its ability to undergo palladium-catalyzed cyclotrimerization, which results in the formation of hexafluoroand trimethoxytriphenylene derivatives. 2-Bromo-4,5-difluorophenol is a colorless to yellow liquid and holds potential applications in various industries due to its unique chemical properties.

Uses

Used in Pharmaceutical Industry:
2-Bromo-4,5-difluorophenol is used as an intermediate compound for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, particularly those targeting specific biological pathways or receptors.
Used in Chemical Synthesis:
In the field of chemical synthesis, 2-Bromo-4,5-difluorophenol is utilized as a building block for creating more complex organic molecules. Its reactivity and structural features make it a valuable precursor in the synthesis of various specialty chemicals, including those with potential applications in materials science, agrochemicals, and other industrial sectors.
Used in Material Science:
2-Bromo-4,5-difluorophenol is used as a component in the development of advanced materials, such as polymers and coatings, due to its ability to undergo specific chemical reactions. Its incorporation into these materials can enhance their properties, such as thermal stability, chemical resistance, or mechanical strength.
Used in Research and Development:
As a versatile organic compound, 2-Bromo-4,5-difluorophenol is employed in research and development laboratories for studying its properties and potential applications. It serves as a model compound for understanding the behavior of similar molecules and for testing new synthetic methods or reaction conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 166281-37-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,2,8 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 166281-37:
(8*1)+(7*6)+(6*6)+(5*2)+(4*8)+(3*1)+(2*3)+(1*7)=144
144 % 10 = 4
So 166281-37-4 is a valid CAS Registry Number.
InChI:InChI=1/C7H4BF6.K/c9-7(10,11)5-1-3-6(4-2-5)8(12,13)14;/h1-4H;/q-1;+1

166281-37-4 Well-known Company Product Price

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  • Alfa Aesar

  • (L16716)  2-Bromo-4,5-difluorophenol, 97%   

  • 166281-37-4

  • 1g

  • 315.0CNY

  • Detail
  • Alfa Aesar

  • (L16716)  2-Bromo-4,5-difluorophenol, 97%   

  • 166281-37-4

  • 5g

  • 989.0CNY

  • Detail

166281-37-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-4,5-difluorophenol

1.2 Other means of identification

Product number -
Other names 2-bromo-4,5-diflouo phenol

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:166281-37-4 SDS

166281-37-4Upstream product

166281-37-4Relevant articles and documents

Construction of Phenanthrenes and Chrysenes from β-Bromovinylarenes via Aryne Diels-Alder Reaction/Aromatization

Singh, Vikram,Verma, Ram Subhawan,Khatana, Anil K.,Tiwari, Bhoopendra

supporting information, p. 14161 - 14167 (2019/10/28)

A highly efficient transition-metal-free general method for the synthesis of polycyclic aromatic hydrocarbons like phenanthrenes and chrysenes (and tetraphene) from β-bromovinylarenes and arynes has been developed. The reactions proceed via an aryne Diels-Alder (ADA) reaction, followed by a facile aromatization. This is the first report on direct construction of chrysenes (and tetraphene) using the ADA approach. Unlike the literature method which is limited to only 9/10-substituted derivatives, this method gives access to a wide variety of functionalized phenanthrenes.

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