BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I)

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BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I) Basic information
Reaction
Product Name:BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I)
Synonyms:BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I);Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I),min.97%;Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I), min. 97%;BroMo(1,10-phenanthroline)(triphenylphosphine)copper(I),97%;Bromo(1,10-phenanthroline)(triphenylphosphine)copper;10-phenanthroline)(triphenylphosphine)copper(I);Bromo(1;(1,10-Phenanthroline)(triphenylphosphine) Copper(I) bromide
CAS:25753-84-8
MF:C30H25BrCuN2P
MW:587.97
EINECS:
Product Categories:Cu;metal amine complex
Mol File:25753-84-8.mol
BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I) Structure
BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I) Chemical Properties
storage temp. 2-8°C, protect from light, stored under nitrogen
form Powder
color yellow
Safety Information
Risk Statements 36/37/38
Safety Statements 26-36/37/39
MSDS Information
BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I) Usage And Synthesis
ReactionCopper-catalyzed coupling of imidazoles and pyrazoles with 1,1-dibromo-1-alkenes: a distinct approach for direct Nalkynylation of heteroarenes.
Synthesis of benzoindoloquinolizines via a Cu(I)-mediated C-N bond formation.
Efficient synthesis of 1,4-disubstituted triazolyl N-carboxamides via a simple and convenient MCR using basic alumina as a solid support.
Cu(I) complexes with diethoxyphosphoryl-1,10-phenanthrolines in catalysis of C-C and C-heteroatom bond formation. Reactions of 25753-84-8_1
Reactions of 25753-84-8_2
BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I) Preparation Products And Raw materials
Tag:BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I)(25753-84-8) Related Product Information
Cuprous bromide BROMO(1,10-PHENANTHROLINE)(TRIPHENYLPHOSPHINE)COPPER (I)