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CAS

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1395063-66-7

(E)-2-methyl-4'-styryl-1,1'-biphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1395063-66-7 Structure

  • Basic information

    1. Product Name: (E)-2-methyl-4'-styryl-1,1'-biphenyl
    2. Synonyms:
    3. CAS NO:1395063-66-7
    4. Molecular Formula:
    5. Molecular Weight: 270.374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1395063-66-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (E)-2-methyl-4'-styryl-1,1'-biphenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-2-methyl-4'-styryl-1,1'-biphenyl(1395063-66-7)
    11. EPA Substance Registry System: (E)-2-methyl-4'-styryl-1,1'-biphenyl(1395063-66-7)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 1395063-66-7(Hazardous Substances Data)

1395063-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1395063-66-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,0,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1395063-66:
(9*1)+(8*3)+(7*9)+(6*5)+(5*0)+(4*6)+(3*3)+(2*6)+(1*6)=177
177 % 10 = 7
So 1395063-66-7 is a valid CAS Registry Number.

1395063-66-7Downstream Products

1395063-66-7Relevant articles and documents

Pd(0)-Catalyzed Tandem One-Pot Reaction of Biphenyl Ketones/Aldehydes to the Corresponding Di-substituted Aryl Olefins

Liu, Yang,Liu, Ping,Liu, Yan,Wei, Yu

, p. 1141 - 1148 (2017/07/25)

Synthesis of di-substituted aryl olefins via a Pd(0)-catalyzed cross-coupling reaction of biphenyl ketones/aldehydes, tosylhydrazide, and aryl bromides (or benzyl halides) was developed. This methodology was achieved by one-pot two-step reactions involvin

1-(α-Aminobenzyl)-2-naphthol as phosphine-free ligand for Pd-catalyzed Suzuki and one-pot Wittig-Suzuki reaction

Chaudhary,Bedekar

experimental part, p. 430 - 437 (2012/09/22)

Air stable and easily accessible, 1-(α-aminobenzyl)-2-naphthols are used as efficient phosphine-free ligands in palladium-catalyzed Suzuki reaction for a variety of substrates under conventional heating as well as ultrasonic conditions. Multi-brominated aromatic substrates were successfully converted to corresponding arylated moieties with good conversion and selectivity. A novel one-pot two-step cascade reaction strategy involving Wittig and Suzuki reactions is developed for efficient synthesis of 4-styryl biphenyls (C 6-C2-C6-C6 unit). Copyright 2012 John Wiley & Sons, Ltd. Phosphine free 1-(α-aminobenzyl)-2- naphthol ligands are used for Pd catalyzed Suzuki and one-pot Wittig-Suzuki reaction to efficiently prepare styryl biphenyls (C6-C 2-C6-C6 unit). Copyright

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