Bis(triphenylphosphine)nickel(II)chloride

$ 1.00 /1KG

career henan chemical co

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China

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Chemical Properties

Product Name	Bis(triphenylphosphine)nickel(II)chloride
CAS No	14264-16-5
EC-No	238-154-8
Min. Order	1G
Purity	98%
Supply Ability	1000KG
Release date	2019/07/06

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Bis(triphenylphosphine)nickel(II)chloride Basic information

Reaction

Product Name:	Bis(triphenylphosphine)nickel(II)chloride
Synonyms:	Bis (triphenylphosphine) nickel chloride;NiCl2(PPh3)2;Bis(triphenylphosphine)nickel(II) dichloride 99.99% trace metals basis;Bis(triphenylphosphine)nickel(II) dichloride synthesis grade;Bis(triphenylphosphine)nickel(II)chloride,(PPh3)2NiCl2;Bis(triphenylphosphine)nickel(II) chloride for synthesis;Bis(tri-N-butylphosphine)dichloronickel;bis(triphenylphosphine)dichloro-nicke
CAS:	14264-16-5
MF:	C36H30Cl2NiP2
MW:	654.17
EINECS:	238-154-8
Product Categories:	Pyridines;Ni;Catalysts for Organic Synthesis;Classes of Metal Compounds;Homogeneous Catalysts;Metal Complexes;Ni (Nickel) Compounds;Synthetic Organic Chemistry;Transition Metal Compounds;metal-phosphine complexes;Aromatics;Phosphorylating and Phosphitylating Agents;Metal Compounds
Mol File:	14264-16-5.mol

Bis(triphenylphosphine)nickel(II)chloride Chemical Properties

Melting point	250 °C (dec.)(lit.)
storage temp.	Store below +30°C.
form	Crystals or Powder
color	Dark green to dark gray
Water Solubility	insoluble
Sensitive	Hygroscopic
CAS DataBase Reference	14264-16-5(CAS DataBase Reference)
NIST Chemistry Reference	dichlorobis(triphenylphosphine)nickel(14264-16-5)

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MSDS Information

Provider	Language
Dichlorobis(triphenylphosphine)nickel(II)	English
ACROS	English
SigmaAldrich	English
ALFA	English

Bis(triphenylphosphine)nickel(II)chloride Usage And Synthesis

Reaction	Catalyst for hydrosilylation of styrene with diphenysilane Catalyst for carboxylation of various aryl chlorides and other derivatives Catalyst for C–P cross-coupling reactions of diphenylphosphine oxide with aryl chloride Catalyst for N?Heterocyclic carbene-assisted cross-coupling reactions of diarylborinic acids with aryl chlorides,tosylates, and sulfamates. Catalyst for Negishi biaryl ketone synthesis by cross-coupling of amides with aryl zinc halides via carbon-nitrogen bond cleavage.
Chemical Properties	dark green to dark grey crystals or powder
Uses	Coordination compund.
Uses	suzuki reaction

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