4-amino-N-benzyl-N-methylbenzamide

Base Information

Chemical Name:4-amino-N-benzyl-N-methylbenzamide
CAS No.:85592-78-5
Molecular Formula:C15H16N2O
Molecular Weight:240.30000
Hs Code.:
ChEMBL ID:CHEMBL164649
DSSTox Substance ID:DTXSID50602659
Wikidata:Q82499801
Mol file:85592-78-5.mol

Synonyms:4-amino-N-benzyl-N-methylbenzamide;85592-78-5;Benzamide, 4-amino-N-methyl-N-(phenylmethyl)-;CHEMBL164649;SCHEMBL19630546;DTXSID50602659;BBL031499;STK899004;AKOS000151422;VS-10548

Suppliers and Price of 4-amino-N-benzyl-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

Matrix Scientific
4-Amino-N-benzyl-N-methylbenzamide
500mg
$ 199.00

Total 3 raw suppliers

Chemical Property of 4-amino-N-benzyl-N-methylbenzamide

Chemical Property:

PSA：46.33000
LogP:3.12220
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:240.126263138
Heavy Atom Count:18
Complexity:266

Purity/Quality:

98%min ^*data from raw suppliers

4-Amino-N-benzyl-N-methylbenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CC1=CC=CC=C1)C(=O)C2=CC=C(C=C2)N

Technology Process of 4-amino-N-benzyl-N-methylbenzamide

There total 2 articles about 4-amino-N-benzyl-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:

: 122-04-3
4-nitro-benzoyl chloride

: 85592-78-5
N-benzyl-N-methyl-4-(2-oxo-2-phenylacetamido)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / 20percent (w/v) K₂CO₃ / tetrahydrofuran / 12 h / Heating

2: 80 percent / H₂ / 5percent Pd/C / ethanol / 3 h / 2327.2 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00372a013

Reference yield:

: 103-67-3
benzyl-methyl-amine

: 85592-78-5
N-benzyl-N-methyl-4-(2-oxo-2-phenylacetamido)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / 20percent (w/v) K₂CO₃ / tetrahydrofuran / 12 h / Heating

2: 80 percent / H₂ / 5percent Pd/C / ethanol / 3 h / 2327.2 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00372a013

Reference yield:

: 85592-78-5
N-benzyl-N-methyl-4-(2-oxo-2-phenylacetamido)benzamide

: 611-73-4
Benzoylformic acid

: 1618080-56-0
N-benzyl-N-methyl-4-(2-oxo-2-phenylacetamido)benzamide

Guidance literature:: Benzoylformic acid; With thionyl chloride; triethylamine; In dichloromethane; at 0 ℃; for 0.333333h; Inert atmosphere;

N-benzyl-N-methyl-4-(2-oxo-2-phenylacetamido)benzamide; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1039/c4cc02744b