2-benzoyl-N-methylbenzamide

Base Information

Chemical Name:2-benzoyl-N-methylbenzamide
CAS No.:32557-55-4
Molecular Formula:C₁₅H₁₃NO₂
Molecular Weight:239.274
Hs Code.:
European Community (EC) Number:666-230-4
DSSTox Substance ID:DTXSID80877717
Nikkaji Number:J940.554B
Wikidata:Q82859563

Synonyms:2-benzoyl-N-methylbenzamide;32557-55-4;SCHEMBL11504870;DTXSID80877717;AKOS024336456

Suppliers and Price of 2-benzoyl-N-methylbenzamide

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 2-benzoyl-N-methylbenzamide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:239.094628657
Heavy Atom Count:18
Complexity:308

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CNC(=O)C1=CC=CC=C1C(=O)C2=CC=CC=C2

Technology Process of 2-benzoyl-N-methylbenzamide

There total 1 articles about 2-benzoyl-N-methylbenzamide 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:

: 32557-55-4
2-methylcarbamoylbenzophenone

Guidance literature:

Reference yield:

: 32557-55-4
2-methylcarbamoylbenzophenone

: 22686-81-3
3-methyl-2-phenyl-4(3H)-quinazolinone

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) SOCl₂ 2.) tetrabutylammonium azide / 1.) SOCl₂, benzene, 48 h, RT 2.) tetrabutylammonium azide, acetonitrile, 1 h, RT

2: 33 percent / xylene / Heating

With thionyl chloride; tetrabutylammoniun azide; In xylene;

Reference yield:

: 32557-55-4
2-methylcarbamoylbenzophenone

: 84628-31-9,100880-33-9
2,3-dihydro-2-methyl-3-phenyliminoisoindol-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 1.) SOCl₂ 2.) tetrabutylammonium azide / 1.) SOCl₂, benzene, 48 h, RT 2.) tetrabutylammonium azide, acetonitrile, 1 h, RT

2: 28 percent / xylene / Heating

With thionyl chloride; tetrabutylammoniun azide; In xylene;