1063716-38-0

Basic information

• Product Name: (acetato){benzo[h]quinolin-10-yl-(4-nitrophenylsulfonyl)amide}(pyridine)palladium(II)
• Synonyms: (acetato){benzo[h]quinolin-10-yl-(4-nitrophenylsulfonyl)amide}(pyridine)palladium(II)
• CAS NO: 1063716-38-0
• Molecular Weight: 622.954
• Mol File: 1063716-38-0.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (acetato){benzo[h]quinolin-10-yl-(4-nitrophenylsulfonyl)amide}(pyridine)palladium(II)(CAS DataBase Reference)
• NIST Chemistry Reference: (acetato){benzo[h]quinolin-10-yl-(4-nitrophenylsulfonyl)amide}(pyridine)palladium(II)(1063716-38-0)
• EPA Substance Registry System: (acetato){benzo[h]quinolin-10-yl-(4-nitrophenylsulfonyl)amide}(pyridine)palladium(II)(1063716-38-0)

Safety Data

• Hazardous Substances Data: 1063716-38-0(Hazardous Substances Data)

Upstream product

• 110-86-1 pyridine 
• 31114-75-7 bis(benzo[h]quinolinato-C(12)N(1))(μ-chlorido)palladium(II) 
• 563-63-3 silver(I) acetate 
• 1176917-20-6 PdCl(N(C₆H₄NO₂)C₁₃H₈N)(pyridine) 

Downstream Products

• 1063716-56-2 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄C(CH₃)3) 
• 1063716-78-8 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄Br) 
• 1063716-71-1 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄OH) 
• 1063716-83-5 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₃ClCH₃) 
• 1063716-69-7 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄CONH₂) 
• 1063716-87-9 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₃C₂H₂NC(O)OC(CH₃)3) 
• 1063716-51-7 (phenyl){benzo[h]quinolin-10-yl-(4-nitrophenylsulfonyl)amide}(pyridine)palladium(II) 
• 1063716-75-5 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄OCH₃) 
• 1063716-66-4 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄CHO) 
• 1063716-85-7 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄CF₃) 
• 1063716-60-8 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄C₆H₅) 
• 1063716-63-1 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(C₆H₄CH₂OH) 
• 1176917-20-6 PdCl(N(C₆H₄NO₂)C₁₃H₈N)(pyridine) 
• 1176325-48-6 Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(NCCH₃)⁽¹⁺⁾*BF₄^(1-)=(Pd(C₅H₅N)(C₁₃H₈N₂SO₂C₆H₄NO₂)(NCCH₃))(BF₄) 

Relevant articles and documents

Palladium-mediated fluorination of arylboronic acids

(Chemical Equation Presented) Saving the best for last: Novel palladium complexes allow mild, two-step fluorination of aryl boronic acids (see scheme). The reaction is regiospecific, functional-group tolerant, has a broad substrate scope, and is ideally suited for the introduction of fluorine substituents at a late stage for aryl fluoride synthesis.