N-Benzyl-3-benzyloxy-2-pyridone

Base Information

Chemical Name:N-Benzyl-3-benzyloxy-2-pyridone
CAS No.:24016-11-3
Molecular Formula:C19H17 N O2
Molecular Weight:291.349
Hs Code.:2933399090
European Community (EC) Number:245-984-4
NSC Number:294819
DSSTox Substance ID:DTXSID10178749
Nikkaji Number:J236.726B
Wikidata:Q83049225
ChEMBL ID:CHEMBL2138619
Mol file:24016-11-3.mol

Synonyms:N-Benzyl-3-benzyloxy-2-pyridone;24016-11-3;MLS003115681;EINECS 245-984-4;1-Benzyl-3-benzyloxy-2(1H)-pyridone;2(1H)-Pyridone, 1-benzyl-3-(benzyloxy)-;NSC294819;SCHEMBL271730;CHEMBL2138619;DTXSID10178749;NSC 294819;NSC-294819;1-Benzyl-3-benzyloxy-1H-pyridin-2-one;1-Benzyl-3-(benzyloxy)-2(1H)-pyridone;SMR001831252;1-Benzyl-3-(benzyloxy)pyridine-2(1H)-one;1-Benzyl-3-(benzyloxy)-2(1H)-pyridinone #;1-benzyl-3-(benzyloxy)-1,2-dihydropyridin-2-one;2(1H)-Pyridinone, 3-(phenylmethoxy)-1-(phenylmethyl)-

Suppliers and Price of N-Benzyl-3-benzyloxy-2-pyridone

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 5 raw suppliers

Chemical Property of N-Benzyl-3-benzyloxy-2-pyridone

Chemical Property:

Vapor Pressure:2.36E-11mmHg at 25°C
Melting Point:113-116oC
Boiling Point:530.9°Cat760mmHg
Flash Point:274.9°C
PSA：31.23000
Density:1.2g/cm³
LogP:3.47560
XLogP3:3.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:291.125928785
Heavy Atom Count:22
Complexity:429

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

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: S24/25:Avoid contact with skin and eyes.;

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN2C=CC=C(C2=O)OCC3=CC=CC=C3

Technology Process of N-Benzyl-3-benzyloxy-2-pyridone

There total 3 articles about N-Benzyl-3-benzyloxy-2-pyridone 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: 66.0%