(1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate dichloromethane adduct

• Catalog Number: ACM33989105
• Product Name: (1,10-Phenanthroline)bis(triphenylphosphine)copper(I) nitrate dichloromethane adduct
• CAS: 33989-10-5
• Category: Heterocyclic Organic Compound
• Synonyms: 33989-10-5, SC10053, BIS COPPER NITRATEDICHLOROMETHANEADDUCT
• IUPAC Name: copper(1+);dichloromethane;1,10-phenanthroline;triphenylphosphane;nitrate
• Molecular Weight: 915.26
• Molecular Formula: [Cu(C12H8N2)[P(C6H5)3]2]NO3 · 1/2CH2Cl2
• Canonical SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.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.C(Cl)Cl.[N+](=O)([O-])[O-].[Cu+]
• InChI Key: RMYGTLXCRLUAKL-UHFFFAOYSA-N
• Application: High yield synthesis of 2-arylbenzo[b]furans via the copper (I) catalyzed coupling of o-iodophenols and aryl acetylenes.; ; High yield synthesis of vinyl sulfides.; ; Efficient synthesis of 1,3-enynes.; ; Effective synthesis of 2-substituted indoles.; ; Synthesis of 1,4-disubstituted 5-iodotriazoles.; ; Selective cyclization strategy to 2-substitued benzofurans and indoles.; ; Copper-catalyzed cascade reaction to 2-indolyl-C-glycosides.
• Exact Mass: 913.12200
• H-Bond Acceptor: 5
• H-Bond Donor: 0
• Safety Description: 26-36/37/39