N-(2-carbamoylphenyl)-3,4,5-trimethoxybenzamide

Base Information

Chemical Name:N-(2-carbamoylphenyl)-3,4,5-trimethoxybenzamide
CAS No.:55695-67-5
Molecular Formula:C₁₇H₁₈N₂O₅
Molecular Weight:330.34
Hs Code.:
DSSTox Substance ID:DTXSID40357823
Nikkaji Number:J1.508.569J
Wikidata:Q82137967
ChEMBL ID:CHEMBL153209

Synonyms:N-(2-carbamoylphenyl)-3,4,5-trimethoxybenzamide;55695-67-5;ST50646632;CBMicro_028716;Oprea1_831843;CHEMBL153209;SCHEMBL8638460;DTXSID40357823;STK413097;AKOS003000678;BIM-0028763.P001;SR-01000217743;SR-01000217743-1;Z57407839

Suppliers and Price of N-(2-carbamoylphenyl)-3,4,5-trimethoxybenzamide

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of N-(2-carbamoylphenyl)-3,4,5-trimethoxybenzamide

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:330.12157168
Heavy Atom Count:24
Complexity:431

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OC)OC)C(=O)NC2=CC=CC=C2C(=O)N

Technology Process of N-(2-carbamoylphenyl)-3,4,5-trimethoxybenzamide

There total 4 articles about N-(2-carbamoylphenyl)-3,4,5-trimethoxybenzamide 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:

: 552-16-9,104810-18-6
ortho-nitrobenzoic acid

: 55695-67-5
N-(2-Carbamoyl-phenyl)-3,4,5-trimethoxy-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: diphenylphosphoryl chloride; Et₃N / CHCl₃

1.2: NH₃

2.1: H₂ / 5 percent Pd/C / ethanol

3.1: Et₃N / CH₂Cl₂

With hydrogen; triethylamine; Diphenylphosphinic chloride; palladium on activated charcoal; In ethanol; dichloromethane; chloroform;
DOI:10.1016/S0960-894X(00)00717-4

Reference yield:

: 610-15-1
2-nitrobenzamide

: 55695-67-5
N-(2-Carbamoyl-phenyl)-3,4,5-trimethoxy-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: H₂ / 5 percent Pd/C / ethanol

2: Et₃N / CH₂Cl₂

With hydrogen; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1016/S0960-894X(00)00717-4