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[1,1'-Biphenyl]-4,4'-dimethanol,a4,a4,a4',a4'-tetraphenylis a complex organic compound characterized by a central biphenyl unit with two hydroxyl groups at the 4 and 4' positions. Additionally, it features four phenyl rings attached to the 1 and 1' positions of the biphenyl unit. This unique molecular structure endows it with distinctive properties and reactivity, making it a promising candidate for various applications in organic synthesis, polymer chemistry, and materials science.

35377-93-6

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35377-93-6 Usage

Uses

Used in Organic Synthesis:
[1,1'-Biphenyl]-4,4'-dimethanol,a4,a4,a4',a4'-tetraphenylis used as a key intermediate in the synthesis of various organic compounds. Its unique structural features and functional groups allow for the creation of a wide range of molecules with diverse properties and applications.
Used in Polymer Chemistry:
In the field of polymer chemistry, [1,1'-Biphenyl]-4,4'-dimethanol,a4,a4,a4',a4'-tetraphenylserves as a valuable building block for the development of novel polymers. Its incorporation into polymer structures can lead to materials with enhanced properties, such as improved mechanical strength, thermal stability, and chemical resistance.
Used in Materials Science:
[1,1'-Biphenyl]-4,4'-dimethanol,a4,a4,a4',a4'-tetraphenylis utilized in materials science for the development of advanced materials with specific properties. Its unique molecular structure and functional groups can contribute to the creation of materials with tailored characteristics, such as enhanced electrical conductivity, optical properties, or biocompatibility, depending on the intended application.
Used in Pharmaceutical Industry:
[1,1'-Biphenyl]-4,4'-dimethanol,a4,a4,a4',a4'-tetraphenylis used as a starting material or intermediate in the synthesis of various pharmaceutical compounds. Its unique structural features and functional groups can be exploited to design and develop new drugs with improved efficacy, selectivity, and safety profiles.
Used in Chemical Research:
In the realm of chemical research, [1,1'-Biphenyl]-4,4'-dimethanol,a4,a4,a4',a4'-tetraphenylserves as a valuable model compound for studying various aspects of chemistry, such as reaction mechanisms, molecular interactions, and the effects of structural modifications on chemical properties. This knowledge can be applied to the development of new synthetic strategies, catalysts, and materials with improved performance and functionality.

Check Digit Verification of cas no

The CAS Registry Mumber 35377-93-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,3,7 and 7 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35377-93:
(7*3)+(6*5)+(5*3)+(4*7)+(3*7)+(2*9)+(1*3)=136
136 % 10 = 6
So 35377-93-6 is a valid CAS Registry Number.

35377-93-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-[4-[hydroxy(diphenyl)methyl]phenyl]phenyl]-diphenylmethanol

1.2 Other means of identification

Product number -
Other names 4,4'-bis(diphenylhydroxymethyl)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:35377-93-6 SDS

35377-93-6Relevant academic research and scientific papers

Organic nano-grid and preparation method thereof (by machine translation)

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Paragraph 0043-0045, (2020/10/21)

The nano lattice material is a kind of organic nano-frame material taking diphenyl or fluorenyl as an angle tip group, has a regular 'mouth' type structure, can be used as a semiconductor material to an organic electronic device, and has a structural gene

Complexation with Diol Host Compounds. Part 10. Synthesis and Solid State Inclusion Properties of Bis(diarylhydroxymethyl)-substituted Benzenes and Biphenyls; X-Ray Crystal Structures of Two Host Polymorphs and of a Non-functional Host Analogue

Weber, Edwin,Skobridis, Konstantinos,Wierig, Andreas,Nassimbeni, Luigi R.,Johnson, Louise

, p. 2123 - 2130 (2007/10/02)

A new family of host molecules where the molecular axis of usual 'wheel-and-axle' compounds is replaced by aromatic units is described.These diol hosts form crystalline inclusions with a variety of uncharged organic molecules mainly of a polar nature (53

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