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255835-82-6

2-(Dicyclohexylphosphino)-2'-methoxybiphenyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 255835-82-6 Structure

  • Basic information

    1. Product Name: 2-(Dicyclohexylphosphino)-2'-methoxybiphenyl
    2. Synonyms: 2-(Dicyclohexylphosphino)-2'-methoxybiphenyl;Dicyclohexyl(2'-Methoxy-[1,1'-biphenyl]-2-yl)phosphine;2-(DicyclohexylphosphiNA)-2'-Methoxybiphenyl;Dicyclohexyl(2'-Methoxy-2-biphenylyl)phosphine;dicyclohexyl-[2-(2-methoxyphenyl)phenyl]phosphane;Dicyclohexyl(2'-methoxybiphenyl-2-yl)phosphine;Dicyclohexyl(2'-methoxy-[1,1'-biphenyl]-2-yl)
    3. CAS NO:255835-82-6
    4. Molecular Formula: C25H33OP
    5. Molecular Weight: 380.502681
    6. EINECS: 1312995-182-4
    7. Product Categories: N/A
    8. Mol File: 255835-82-6.mol

  • Chemical Properties

    1. Melting Point: 120-122℃
    2. Boiling Point: 504.7±33.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(Dicyclohexylphosphino)-2'-methoxybiphenyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(Dicyclohexylphosphino)-2'-methoxybiphenyl(255835-82-6)
    11. EPA Substance Registry System: 2-(Dicyclohexylphosphino)-2'-methoxybiphenyl(255835-82-6)

  • 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: 255835-82-6(Hazardous Substances Data)

255835-82-6 Usage

Uses

suzuki reaction

Check Digit Verification of cas no

The CAS Registry Mumber 255835-82-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,5,8,3 and 5 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 255835-82:
(8*2)+(7*5)+(6*5)+(5*8)+(4*3)+(3*5)+(2*8)+(1*2)=166
166 % 10 = 6
So 255835-82-6 is a valid CAS Registry Number.

255835-82-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name dicyclohexyl-[2-(2-methoxyphenyl)phenyl]phosphane

1.2 Other means of identification

Product number -
Other names dicyclohexyl-(6'-methoxybiphenyl-2-yl)phosphine

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:255835-82-6 SDS

255835-82-6Relevant articles and documents

Ligands for metals and improved metal-catalyzed processes based thereon

-

, (2008/06/13)

One aspect of the present invention relates to ligands for transition metals. A second aspect of the present invention relates to the use of catalysts comprising these ligands in transition metal-catalyzed carbon-heteroatom and carbon-carbon bond-forming reactions. The subject methods provide improvements in many features of the transition metal-catalyzed reactions, including the range of suitable substrates, reaction conditions, and efficiency.

Ligands for metals and improved metal-catalyzed processes based thereon

-

, (2008/06/13)

One aspect of the present invention relates to novel ligands for transition metals. A second aspect of the present invention relates to the use of catalysts comprising these ligands in transition metal-catalyzed carbon-heteroatom and carbon-carbon bond-forming reactions. The subject methods provide improvements in many features of the transition metal-catalyzed reactions, including the range of suitable substrates, reaction conditions, and efficiency.

Use of polymer-supported dialkylphosphinobiphenyl ligands for palladium-catalyzed amination and Suzuki reactions

Parrish,Buchwald

, p. 3820 - 3827 (2007/10/03)

The preparations of polymer-supported dialkylphosphinobiphenyl ligands (3) are reported. A palladium catalyst based on ligand 3a is active for amination and Suzuki reactions using unactivated aryl iodides, bromides, or chlorides. Filtration of the catalyst from the reaction mixtures allows for simplified product isolation via an aqueous workup. The resin-bound catalyst can be recycled without additional palladium in both the amination and Suzuki reactions.

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