5-Ethyl-5-phenyl-1,3-diazinan-2-one

Base Information

Chemical Name:5-Ethyl-5-phenyl-1,3-diazinan-2-one
CAS No.:2596-67-0
Molecular Formula:C₁₂H₁₆N₂O
Molecular Weight:204.272
Hs Code.:
NSC Number:84938
DSSTox Substance ID:DTXSID80292704
Wikidata:Q82031117
Mol file:2596-67-0.mol

Synonyms:2596-67-0;5-ethyl-5-phenyl-1,3-diazinan-2-one;NSC84938;DTXSID80292704;NSC-84938

Suppliers and Price of 5-Ethyl-5-phenyl-1,3-diazinan-2-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
Packaging
price

Total 6 raw suppliers

Chemical Property of 5-Ethyl-5-phenyl-1,3-diazinan-2-one

Chemical Property:

Vapor Pressure:4.31E-07mmHg at 25°C
Boiling Point:414.9°Cat760mmHg
Flash Point:176.1°C
Density:1.046g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:204.126263138
Heavy Atom Count:15
Complexity:224

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC1(CNC(=O)NC1)C2=CC=CC=C2

Technology Process of 5-Ethyl-5-phenyl-1,3-diazinan-2-one

There total 5 articles about 5-Ethyl-5-phenyl-1,3-diazinan-2-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:

: 50-06-6
phenobarbital

: 2596-67-0
phenobarbital

Guidance literature:: With lithium aluminium tetrahydride; diethyl ether;
DOI:10.1021/ja01596a038

Reference yield:

: 80544-75-8
(rac)-2-Cyan-2-phenylbutanamid

: 2596-67-0
phenobarbital

Guidance literature:: Multi-step reaction with 2 steps

1: LiAlH₄; AlCl₃; diethyl ether / Reagens 4: THF

With lithium aluminium tetrahydride; aluminium trichloride; diethyl ether;
DOI:10.1021/ja01571a046