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Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I)

Catalog Number
ACM25753848
Product Name
Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I)
Structure
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CAS
25753-84-8
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Synonyms
Bromocopper;1,10-phenanthroline;triphenylphosphane
Molecular Weight
585.9
Molecular Formula
C30H23BrCuN2P
Canonical SMILES
C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC2=C(C3=C(C=CC=N3)C=C2)N=C1.[Cu]Br
InChI
InChI=1S/C18H15P.C12H8N2.BrH.Cu/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18;1-3-9-5-6-10-4-2-8-14-12(10)11(9)13-7-1;/h1-15H;1-8H;1H;/q;+1/p-1
InChI Key
XKXXFZLAZILJJE-UHFFFAOYSA-M
Purity
98%
Appearance
Powder
Exact Mass
584.00782
Monoisotopic Mass
584.00782
Rotatable Bond Count
3
Topological Polar Surface Area
25.8 Ų
Application
Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I) serves as a catalyst for the copper-catalyzed coupling of imidazoles and pyrazoles with 1,1-dibromo-1-alkenes. This reaction offers a novel and efficient pathway for the direct N-alkynylation of heteroarenes, improving the synthesis of complex organic compounds. By facilitating the formation of new C-N bonds, Bromo(1,10-phenanthroline)(triphenylphosphine)copper(I) expands the potential of copper-catalyzed methodologies in organic synthesis, thereby streamlining the production of diverse chemical entities with applications in pharmaceuticals, material science, and fine chemical industries.
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