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1,1'-Biphenyl, 3,5-dimethoxy- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

64326-17-6

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64326-17-6 Usage

Structure

1,1'-Biphenyl with two methoxy groups at the 3 and 5 positions

Explanation

The compound consists of two benzene rings connected by a single bond, with methoxy groups (CH3O-) attached to the 3 and 5 positions of the biphenyl structure.

Explanation

1,1'-Biphenyl, 3,5-dimethoxyis a derivative of biphenyl, which is a basic structure consisting of two benzene rings connected by a single bond.

Explanation

The presence of two methoxy groups at the 3 and 5 positions of the biphenyl structure gives 1,1'-Biphenyl, 3,5-dimethoxyits unique chemical properties, which may differ from those of the parent compound, biphenyl.

Explanation

1,1'-Biphenyl, 3,5-dimethoxyis used in organic synthesis as a building block for the preparation of other compounds. It is also known for its potential pharmaceutical applications due to its structural similarity to other biologically active molecules.

Explanation

The specific uses and properties of 1,1'-Biphenyl, 3,5-dimethoxymay differ based on the particular application it is being used for, such as in the synthesis of specific compounds or in pharmaceutical research.

Explanation

Due to its structural similarity to other molecules with biological activity, 1,1'-Biphenyl, 3,5-dimethoxyhas potential pharmaceutical applications and may be studied for its interactions with biological systems.

Derivative of biphenyl

Yes

Chemical properties

Unique due to the presence of methoxy groups

Applications

Organic synthesis and pharmaceuticals

Specific uses

Vary depending on the application

Biological activity

Structural similarity to other biologically active molecules

Check Digit Verification of cas no

The CAS Registry Mumber 64326-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,2 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64326-17:
(7*6)+(6*4)+(5*3)+(4*2)+(3*6)+(2*1)+(1*7)=116
116 % 10 = 6
So 64326-17-6 is a valid CAS Registry Number.

64326-17-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-dimethoxy-5-phenylbenzene

1.2 Other means of identification

Product number -
Other names 3,5-dimethoxybiphenyl

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:64326-17-6 SDS

64326-17-6Relevant academic research and scientific papers

Suzuki- and Heck-type cross-coupling with palladium nanoparticles immobilized on spherical polyelectrolyte brushes

Proch,Mei,Rivera Villanueva,Lu,Karpov,Ballauff,Kempe

, p. 493 - 500 (2008)

We report on a systematic study of the use of palladium nanoparticlesimmo bilized on spherical polyelectrolyte brushes - Pd@SPB - for Heck- and Suzuki-type coupling reactions. The spherical polyelectrolyte brush particles serving as carriers for the palladium nanoparticles consist of a solid polystyrene core with a radiusof 46 nm onto which long chains of cationic polyelectrolytesare grafted. The palladium nanoparticles have directly been generated within this brush layer and the stabilization of the nanoparticlesis effected by the colloidal carriers, no further surface stabilization is necessary. We demonstrate that these composite particles present robust catalysts for the Heck- and Suzuki-type coupling reactions. This was shown by carrying out the Suzuki- and Heck-type coupling reactionsat relatively low temperatures (Suzuki reaction: 50°C, Heck reaction: 70°C). We demonstrate that the catalytic composite particles are not changed by these reaction conditions and retain their full activity for at least four runs. The yields obtained for both reactions are good to excellent. The mild operation conditions of the palladium nanoparticles are traced back to the absence of surface stabilization. Further mechanistic implications are discussed.

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