BenzaMide, N-[2-(aMinocarbonyl)phenyl]-3-Methoxy-

Base Information

Chemical Name:BenzaMide, N-[2-(aMinocarbonyl)phenyl]-3-Methoxy-
CAS No.:330657-87-9
Molecular Formula:C15H14N2O3
Molecular Weight:270.288
Hs Code.:
Mol file:330657-87-9.mol

Synonyms:BenzaMide, N-[2-(aMinocarbonyl)phenyl]-3-Methoxy-;N-(2-carbaMoylphenyl)-3-MethoxybenzaMide

Suppliers and Price of BenzaMide, N-[2-(aMinocarbonyl)phenyl]-3-Methoxy-

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

ChemScene
Benzamide,N-[2-(aminocarbonyl)phenyl]-3-methoxy-
1g
$ 150.00

Total 7 raw suppliers

Chemical Property of BenzaMide, N-[2-(aMinocarbonyl)phenyl]-3-Methoxy-

Chemical Property:

PSA：81.42000
LogP:2.81970

Purity/Quality:

99% ^*data from raw suppliers

Benzamide,N-[2-(aminocarbonyl)phenyl]-3-methoxy- ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of BenzaMide, N-[2-(aMinocarbonyl)phenyl]-3-Methoxy-

There total 4 articles about BenzaMide, N-[2-(aMinocarbonyl)phenyl]-3-Methoxy- 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: 100.0%

: 1711-05-3
m-anisoyl chloride

: 28144-70-9,88-68-6
anthranilic acid amide

: 330657-87-9
N-(2-carbamoylphenyl)-3-methoxybenzamide

Guidance literature:: With pyridine; In chloroform; at 20 ℃; for 6h;

Reference yield:

: 67836-50-4
2-[(3-methoxybenzoyl)amino]benzoic acid methyl ester

: 330657-87-9
N-(2-carbamoylphenyl)-3-methoxybenzamide

Guidance literature:: With ammonia; In methanol; water;
DOI:10.1016/j.bmc.2006.06.046

Reference yield:

: 1711-05-3
m-anisoyl chloride

: 330657-87-9
N-(2-carbamoylphenyl)-3-methoxybenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: Et₃N / tetrahydrofuran

2: ammonia / H₂O; methanol

With ammonia; triethylamine; In tetrahydrofuran; methanol; water;
DOI:10.1016/j.bmc.2006.06.046