N-(2-cyanophenyl)-2-methoxybenzamide

Base Information

Chemical Name:N-(2-cyanophenyl)-2-methoxybenzamide
CAS No.:708289-25-2
Molecular Formula:C₁₅H₁₂N₂O₂
Molecular Weight:252.272
Hs Code.:
DSSTox Substance ID:DTXSID80356411
Wikidata:Q82135728
Mol file:708289-25-2.mol

Synonyms:N-(2-cyanophenyl)-2-methoxybenzamide;708289-25-2;DTXSID80356411;STL062979;AKOS000185192;AG-670/36127040;SR-01000280210;SR-01000280210-1

Suppliers and Price of N-(2-cyanophenyl)-2-methoxybenzamide

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 1 raw suppliers

Chemical Property of N-(2-cyanophenyl)-2-methoxybenzamide

Chemical Property:

PSA：65.61000
LogP:3.20318
XLogP3:3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:252.089877630
Heavy Atom Count:19
Complexity:360

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=CC=C1C(=O)NC2=CC=CC=C2C#N

Technology Process of N-(2-cyanophenyl)-2-methoxybenzamide

There total 1 articles about N-(2-cyanophenyl)-2-methoxybenzamide 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:

: 21615-34-9
2-Methoxybenzoyl chloride

: 1885-29-6
anthranilic acid nitrile

: 708289-25-2
C₁₅H₁₂N₂O₂

Guidance literature:: With potassium carbonate; In diethyl ether; for 24h; Reflux;
DOI:10.1021/jm101150b

Reference yield: 33.0%

: 708289-25-2
C₁₅H₁₂N₂O₂

: 1028-96-2
2-(2-methoxyphenyl)quinazolin-4-ol

Guidance literature:: With dihydrogen peroxide; sodium hydroxide; In water; for 20h; Reflux;
DOI:10.1021/jm101150b

Reference yield:

: 708289-25-2
C₁₅H₁₂N₂O₂

: C₂₄H₂₈N₄O₃

Guidance literature:: Multi-step reaction with 4 steps

1: dihydrogen peroxide; sodium hydroxide / water / 20 h / Reflux

2: trichlorophosphate / 4.5 h / Reflux

3: boron tribromide / dichloromethane / 24 h

4: triethylamine / dichloromethane

With dihydrogen peroxide; boron tribromide; triethylamine; sodium hydroxide; trichlorophosphate; In dichloromethane; water;
DOI:10.1021/jm101150b