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Home > Products >  Bis(tricyclohexylphosphine)nickel(II) chloride

Bis(tricyclohexylphosphine)nickel(II) chloride CAS NO.19999-87-2

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  • Min.Order: 1 Kilogram
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  • Product Details

Keywords

  • Bis(tricyclohexylphosphine)nickel(II) chloride
  • 19999-87-2
  • 98%

Quick Details

  • ProName: Bis(tricyclohexylphosphine)nickel(II) ...
  • CasNo: 19999-87-2
  • Molecular Formula: 2C18H33P.Cl2Ni
  • Appearance: powder
  • Application: intermediate
  • DeliveryTime: in stock
  • PackAge: according to your need for packing
  • Port: Shanghai
  • ProductionCapacity: 200 Kilogram/Quarter
  • Purity: 98%
  • Storage: dry
  • Transportation: courier,sea,air
  • LimitNum: 1 Kilogram

Superiority

Bis(tricyclohexylphosphine)nickel(II) chloride, 99% Basic information

Properties
Melting point     227-231℃ (DEC.)
CAS DataBase Reference    19999-87-2


MF:    2C18H33P.Cl2Ni
MW:    690.464

Mol File:    19999-87-2.mol

Safety Information
Hazard Codes     Xn
Risk Statements     22-40-43
Safety Statements     53-36/37-45-60
WGK Germany     3

Details

Bis(tricyclohexylphosphine)nickel(II) chloride, 99% Basic information
Reaction
Product Name:    Bis(tricyclohexylphosphine)nickel(II) chloride, 99%

CAS:    19999-87-2
MF:    2C18H33P.Cl2Ni
MW:    690.464

Product Categories:    Ni;metal-phosphine complexes
Mol File:    19999-87-2.mol

Properties
Melting point     227-231℃ (DEC.)
CAS DataBase Reference    19999-87-2

 

Safety Information
Hazard Codes     Xn
Risk Statements     22-40-43
Safety Statements     53-36/37-45-60
WGK Germany     3

 

Reaction    
An approach to five-membered lactams from aliphatic amides and terminal acetylenes by nickel catalysis.
Synthesis of biaryls through nickel-catalyzed Suzuki-Miyaura coupling of amides by carbon-nitrogen bond cleavage.
Ni-catalyzed borylation of aryl fluorides via C-F cleavage.
Nickeland palladium–catalyzed coupling of aryl fluorosulfonates with aryl boronic acids enabled by sulfuryl fluoride.
Nickel-catalyzed one-pot synthesis of biaryls from phenols and arylboronic acids via C-O activation using TCT reagents.

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