1207379-34-7

Basic information

• Product Name: 5-(4-chlorophenyl)-1,3,5,7,9,10-hexahydropyrimido[5',4'-5,6]pyridine[2,3-d]pyrimidine-2,4,6,8-tetraone
• Synonyms: 5-(4-chlorophenyl)-1,3,5,7,9,10-hexahydropyrimido[5',4'-5,6]pyridine[2,3-d]pyrimidine-2,4,6,8-tetraone
• CAS NO: 1207379-34-7
• Molecular Weight: 359.728
• Mol File: 1207379-34-7.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: 5-(4-chlorophenyl)-1,3,5,7,9,10-hexahydropyrimido[5',4'-5,6]pyridine[2,3-d]pyrimidine-2,4,6,8-tetraone(CAS DataBase Reference)
• NIST Chemistry Reference: 5-(4-chlorophenyl)-1,3,5,7,9,10-hexahydropyrimido[5',4'-5,6]pyridine[2,3-d]pyrimidine-2,4,6,8-tetraone(1207379-34-7)
• EPA Substance Registry System: 5-(4-chlorophenyl)-1,3,5,7,9,10-hexahydropyrimido[5',4'-5,6]pyridine[2,3-d]pyrimidine-2,4,6,8-tetraone(1207379-34-7)

Safety Data

• Hazardous Substances Data: 1207379-34-7(Hazardous Substances Data)

Upstream product

• 67-52-7 BARBITURIC ACID 
• 104-88-1 4-chlorobenzaldehyde 
• 873-83-6 4-Amino-2,6-dihydroxypyrimidine 

Relevant articles and documents

Immobilization of Cu(II)on MWCNTs@L-His as a new high efficient reusable catalyst for the synthesis of pyrido[2,3-d:5,6-d′]dipyrimidine derivatives

In this research, a new heterogeneous organometallic catalyst was prepared through Cu(II)Immobilization on L-Histidine Functionalized multi-walled carbon nanotubes (MWCNTs@L-His/Cu(II)). Catalyst was prepared using a simple method and characterized by Fou

Application of SBA-15 functionalized sulfonic acid (SBA-Pr-SO3H) as an efficient nanoreactor in the one-pot synthesis of pyrido[2,3-d]pyrimidine

Sulfonic acid functionalized nanoporous silica (SBA-Pr-SO3H) with a pore size of 6 nm was synthesized using surface modification of Santa Barbara Amorphous (SBA-15). It is a solid acid hexagonally nano-reactor with high surface area and is reus

Hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal-organic framework composite: a novel and versatile tool for the preparation of pyrido[2,3-d:5,6-d′]dipyrimidines

In the current paper, a hexamethylenetetramine-based ionic liquid immobilized on the MIL-101(Cr) metal-organic framework was successfully synthesized as a novel, efficient, and recoverable catalyst for the synthesis of pyrido[2,3-d:5,6-d′]dipyrimidine derivativesviathe reaction of barbituric acid derivatives, 6-aminouracil/6-amino-1,3-dimethyl uracil, and aromatic aldehydes under solvent-free conditions. Characterization of the catalyst was carried out using various methods such as field emission scanning electron microscopy (FE-SEM), energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectrophotometry (FT-IR), and Brunauer-Emmett-Teller (BET). Efficient transformation, short reaction times, excellent yields, easy product isolation, mild conditions, and the potential high recyclability of the organocatalyst are the main features of this protocol.