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4,4'-Bis(4-chlorophenyl)sulfonyl-1,1'-biphenyl is a sulfur-containing organic building block derived from biphenyl, with sulfonyl groups attached to the 4,4' positions of the biphenyl core. 4,4'-Bis(4-chlorophenyl)sulfonyl-1,1'-biphenyl is characterized by its structural complexity and the presence of chlorine atoms on the phenyl rings, which may contribute to its reactivity and potential applications in various chemical processes.

22287-56-5

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22287-56-5 Usage

Uses

Used in Organic Synthesis:
4,4'-Bis(4-chlorophenyl)sulfonyl-1,1'-biphenyl is used as a synthetic intermediate for the creation of various organic compounds. Its unique structure, which includes sulfonyl and chlorophenyl groups, allows it to serve as a versatile building block in the synthesis of complex organic molecules, particularly those with potential applications in pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 4,4'-Bis(4-chlorophenyl)sulfonyl-1,1'-biphenyl is used as a key intermediate in the development of novel drugs. Its structural features can be exploited to design and synthesize new drug candidates with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Materials Science:
4,4'-Bis(4-chlorophenyl)sulfonyl-1,1'-biphenyl can also be utilized in the field of materials science, where it may contribute to the development of advanced materials with specific properties. For example, its incorporation into polymer structures could lead to materials with improved mechanical strength, thermal stability, or chemical resistance.
Used in Chemical Research:
In academic and industrial research settings, 4,4'-Bis(4-chlorophenyl)sulfonyl-1,1'-biphenyl serves as a valuable compound for exploring new reaction pathways and understanding the reactivity of various functional groups. Its synthesis and subsequent transformations can provide insights into the mechanisms of organic reactions and inform the design of new synthetic strategies.

Check Digit Verification of cas no

The CAS Registry Mumber 22287-56-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,8 and 7 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22287-56:
(7*2)+(6*2)+(5*2)+(4*8)+(3*7)+(2*5)+(1*6)=105
105 % 10 = 5
So 22287-56-5 is a valid CAS Registry Number.

22287-56-5 Well-known Company Product Price

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  • Aldrich

  • (440949)  4,4′-Bis[(4-chlorophenyl)sulfonyl]-1,1′-biphenyl  98%

  • 22287-56-5

  • 440949-100G

  • 1,269.45CNY

  • Detail

22287-56-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(4-chlorophenyl)sulfonyl-4-[4-(4-chlorophenyl)sulfonylphenyl]benzene

1.2 Other means of identification

Product number -
Other names 4,4'-bis((4-chlorophenyl)sulfonyl)-1,1'-biphenyl

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:22287-56-5 SDS

22287-56-5Relevant academic research and scientific papers

PROCESS FOR THE MANUFACTURE OF DIHALODIPHENYLSULFONES

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Page/Page column 20; 21, (2012/11/07)

A process for the preparation of dihalodiphenylsulfones_such as 4,4'-dichlorodiphenyl sulfone or 4,4'-bis-(4-chlorophenylsulfonyl)biphenyl with high regioselectivity, at low temperature and in the absence of toxic reagents by reacting together at least one acid, at least one fluorinated anhydride and at least one halobenzene. The invented process is particularly suited for the manufacture of 4,4'-dichlorodiphenyl sulfone.

PROCESS FOR THE MANUFACTURE OF DIHALODIPHENYLSULFONES STARTING FROM ORGANIC ACIDS

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Page/Page column 16; 17, (2012/11/07)

A process for the preparation of dihalodiphenylsulfones_such as 4,4'-dichlorodiphenyl sulfone or 4,4'-bis-(4-chlorophenylsulfonyl)biphenyl with high regioselectivity, at low temperature and in the absence of toxic reagents by reacting together at least one acid, sulfur trioxide and at least one halobenzene. The invented process is particularly suited for the manufacture of 4,4'-dichlorodiphenyl sulfone.

Macrocyclic aromatic polysulfones and sulfide-sulfones: Synthesis and structural characterisation of molecular pentagons and rectangles

Ben-Haida, Abderrazak,Colquhoun, Howard M.,Hodge, Philip,Raftery, James,White, Andrew J.P.,Williams, David J.

scheme or table, p. 5229 - 5235 (2010/04/03)

Cyclo-condensation of arylenedithiols with bis(4-chlorophenylenesulfone)s under pseudo-high-dilution conditions affords macrocyclic aromatic sulfide-sulfones which are readily oxidised to all-sulfone-linked macrocycles. The cyclic pentamer of poly(1,4-phe

Bis(4-hydroxyphenyl sulfonylphenyl) bisphenyl disulfones and useful resins based thereon

-

, (2008/06/13)

The present invention relates to the novel monomers generically identified as bis(4-hydroxyphenyl sulfonylphenyl) biphenyl disulfones, to a process for their production and to their use in the preparation of polycarbonates, polyurethanes, polyesters, polysulfones and polyethers.

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