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2285-29-2

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2285-29-2 Usage

Structure

1,1'-Biphenyl with 2,6-difluoro substitution

Explanation

The compound consists of two benzene rings linked together (biphenyl) with two fluorine atoms attached at the 2 and 6 positions.

Explanation

1,1'-Biphenyl, 2,6-difluorois derived from biphenyl, which is a compound consisting of two benzene rings linked together.

Explanation

The compound is used as a chemical intermediate in the production of various products, including pharmaceuticals, agrochemicals, and other organic compounds.

Explanation

1,1'-Biphenyl, 2,6-difluoromay be used in the development of new materials, such as polymers and liquid crystals, due to its unique properties.

Explanation

The compound may be used in research and development for the synthesis of new compounds with specific properties and functions, which could be beneficial in various industries.

Explanation

The specific chemical properties of 1,1'-Biphenyl, 2,6-difluoroare not provided in the material, but they would likely be influenced by the presence of the fluorine atoms and the biphenyl structure.

Explanation

The specific physical properties of 1,1'-Biphenyl, 2,6-difluoroare not provided in the material, but they would likely include characteristics such as melting point, boiling point, and solubility, which are influenced by the molecular structure and the presence of fluorine atoms.

Derivative of biphenyl

Yes

Industrial applications

Chemical intermediate, pharmaceuticals, agrochemicals, and other organic compounds

Potential uses in materials science

Polymers and liquid crystals

Research and development

Synthesis of new compounds with specific properties and functions

Chemical properties

Unknown (not provided in the material)

Physical properties

Unknown (not provided in the material)

Check Digit Verification of cas no

The CAS Registry Mumber 2285-29-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,2,8 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 2285-29:
(6*2)+(5*2)+(4*8)+(3*5)+(2*2)+(1*9)=82
82 % 10 = 2
So 2285-29-2 is a valid CAS Registry Number.

2285-29-2SDS

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 1,3-difluoro-2-phenylbenzene

1.2 Other means of identification

Product number -
Other names 2,6-difluorobiphenyl

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:2285-29-2 SDS

2285-29-2Relevant articles and documents

Palladium-catalyzed cross-coupling of polyfluoroarenes with simple arenes

Li, Hu,Liu, Jia,Sun, Chang-Liang,Li, Bi-Jie,Shi, Zhang-Jie

supporting information; experimental part, p. 276 - 279 (2011/04/17)

The most efficient method to construct biaryls is the direct dehydrogenative cross-coupling of two different aromatic rings. Such an ideal cross arylation starting from distinct polyfluoroarenes and simple arenes was presented. The selectivity of the cross-coupling was controlled by both of the electronic property of fluoroarenes and steric hindrance of simple arenes. Diisopropyl sulfide was essential to promote the efficacy.

The Photolyses of 2,6- and 2,4-Difluorohalobenzenes

Song, Yong-Qi,Yuzuri, Tomoaki,Suezawa, Hiroko,Sakakibara, Kazuhisa,Hirota, Minoru,Nakada, Masahiro

, p. 1875 - 1878 (2007/10/03)

Photolyses of 2,6- and 2,4-difluorobromobenzenes in acetonitrile gave isomerized and brominated products in addition to 1,3-difluorobenzene produced by the dehalogenation.The reactions were compared with similar reactions of the corresponding chloro- and iodoarenes.In general, photolytic cleavage of the C-X bond of 2,6-difluorohalo(X)benzene was shown to proceed more easily than the corresponding 2,4-difluorohalo compound.

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