2-phenyl-3,5-dihydro-6H-purin-6-one

Base Information

Chemical Name:2-phenyl-3,5-dihydro-6H-purin-6-one
CAS No.:18503-16-7
Molecular Formula:C₁₁H₈N₄O
Molecular Weight:212.211
Hs Code.:
Mol file:18503-16-7.mol

Synonyms:6H-Purin-6-one,1,7-dihydro-2-phenyl- (9CI); Hypoxanthine, 2-phenyl- (7CI,8CI); NSC 210308

Suppliers and Price of 2-phenyl-3,5-dihydro-6H-purin-6-one

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
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price

Total 6 raw suppliers

Chemical Property of 2-phenyl-3,5-dihydro-6H-purin-6-one

Chemical Property:

Vapor Pressure:2.38E-05mmHg at 25°C
Boiling Point:359.4°C at 760 mmHg
Flash Point:171.2°C
Density:1.51g/cm³

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 2-phenyl-3,5-dihydro-6H-purin-6-one

There total 4 articles about 2-phenyl-3,5-dihydro-6H-purin-6-one which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 52.0%

: 82145-23-1
5-Benzamidoimidazole-4-carboxamide

: 18503-16-7
2-Phenylhypoxanthine

Guidance literature:: With potassium hydrogencarbonate; for 4h; Heating;
DOI:10.1002/jhet.5570190104

Reference yield:

: 98-88-4
benzoyl chloride

: 18503-16-7
2-Phenylhypoxanthine

Guidance literature:: Multi-step reaction with 2 steps

1: 68 percent / dimethylaminopyridine / pyridine / 1)r.t. 0.5 h, 2) 50 deg C, 5 h

2: 52 percent / 0.05N aq. KHCO₃ / 4 h / Heating

With dmap; potassium hydrogencarbonate; In pyridine;
DOI:10.1002/jhet.5570190104