2-Benzyl-2H-1,4-benzoxazin-3(4H)-one

Base Information

Chemical Name:2-Benzyl-2H-1,4-benzoxazin-3(4H)-one
CAS No.:62490-89-5
Molecular Formula:C15H13NO2
Molecular Weight:239.274
Hs Code.:
DSSTox Substance ID:DTXSID60493075

Synonyms:62490-89-5;2-Benzyl-2H-1,4-benzoxazin-3(4H)-one;2h-1,4-benzoxazin-3(4h)-one,2-(phenylmethyl)-;SCHEMBL5670687;DTXSID60493075

Suppliers and Price of 2-Benzyl-2H-1,4-benzoxazin-3(4H)-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 0 raw suppliers

Chemical Property of 2-Benzyl-2H-1,4-benzoxazin-3(4H)-one

Chemical Property:

XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:239.094628657
Heavy Atom Count:18
Complexity:299

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)CC2C(=O)NC3=CC=CC=C3O2

Technology Process of 2-Benzyl-2H-1,4-benzoxazin-3(4H)-one

There total 8 articles about 2-Benzyl-2H-1,4-benzoxazin-3(4H)-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: 88.0%

: C₂₃H₂₁NO₃

: 62490-89-5
2-benzyl-2H-benzo[b][1,4]oxazin-3(4H)-one

Guidance literature:: With trifluoroacetic acid; In chloroform; at 70 ℃; for 22h;
DOI:10.1055/a-1523-1597

Reference yield:

: C₂₃H₁₉NO₃

: 62490-89-5
2-benzyl-2H-benzo[b][1,4]oxazin-3(4H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen; palladium 10% on activated carbon / 1,4-dioxane / 20 °C

2: trifluoroacetic acid / chloroform / 22 h / 70 °C

With palladium 10% on activated carbon; hydrogen; trifluoroacetic acid; In 1,4-dioxane; chloroform;
DOI:10.1055/a-1523-1597