1415714-29-2

Basic information

• Product Name: 1-benzyl-4-benzyloxy-3-(4-cyclohexylphenyl)pyridin-2(1H)-one
• Synonyms: 1-benzyl-4-benzyloxy-3-(4-cyclohexylphenyl)pyridin-2(1H)-one
• CAS NO: 1415714-29-2
• Molecular Weight: 449.593
• Mol File: 1415714-29-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1-benzyl-4-benzyloxy-3-(4-cyclohexylphenyl)pyridin-2(1H)-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-benzyl-4-benzyloxy-3-(4-cyclohexylphenyl)pyridin-2(1H)-one(1415714-29-2)
• EPA Substance Registry System: 1-benzyl-4-benzyloxy-3-(4-cyclohexylphenyl)pyridin-2(1H)-one(1415714-29-2)

Safety Data

• Hazardous Substances Data: 1415714-29-2(Hazardous Substances Data)

Upstream product

• 626-03-9 3-deazauracil 
• 96245-97-5 3-bromo-2,4-dihydroxypyridine 
• 586382-62-9 SC-25028 
• 374538-04-2 (4-cyclohexylphenyl)boronic acid 
• 571168-92-8 1-benzyl-4-benzyloxy-3-iodopyridin-2(1H)-one 

Downstream Products

• 1415714-16-7 C₂₂H₂₇NO₆ 
• 1415714-05-4 C₂₈H₃₃NO₉ 

Relevant articles and documents

Practical Pd/C-catalysed suzuki-miyaura reactions for the preparation of 3-aryl-4-oxypyridin-2(1H)-ones, 3-aryl-2,4-oxypyridines and 3-aryl-2,4- oxyquinolines as useful intermediates for the synthesis of biologically active compounds

Practical heterogeneous Pd/C-catalysed Suzuki-Miyaura cross-coupling reactions of 3-iodo-4-oxypyridin-2(1H)-ones, 3-iodo-2,4-oxypyridines, and 3-iodo-2,4-oxyquinolines with arylboronic acids are described as a useful and efficient alternative to homogeneous conditions. The methodology features ligand-free and environmentally friendly conditions, and tolerates a wide range of boronic acids. The cross-coupled products can be viewed as useful intermediates for the preparation of 3-aryl-4-hydroxypyridin-2(1H)-ones, which can be used as new nucleobases for antiherpetic agents.