N-(4-aminophenyl)-N-methylbenzamide

Base Information

Chemical Name:N-(4-aminophenyl)-N-methylbenzamide
CAS No.:63721-85-7
Molecular Formula:C14H14N2O
Molecular Weight:226.278
Hs Code.:
DSSTox Substance ID:DTXSID20395985
Wikidata:Q82196419

Synonyms:N-(4-aminophenyl)-N-methylbenzamide;63721-85-7;n-(4-amino-phenyl)-n-methyl-benzamide;Oprea1_629582;SCHEMBL3454509;DTXSID20395985;STK367001;AKOS001588347;FT-0728603;SR-01000078253;SR-01000078253-1

Suppliers and Price of N-(4-aminophenyl)-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 N-(4-aminophenyl)-N-methylbenzamide

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:226.110613074
Heavy Atom Count:17
Complexity:253

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of N-(4-aminophenyl)-N-methylbenzamide

There total 4 articles about N-(4-aminophenyl)-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:

: 33672-82-1
N-(4-nitrophenyl)-N-methylbenzamide

: 63721-85-7
benzoic acid-(4-amino-N-methyl-anilide)

Guidance literature:: With hydrogenchloride; iron;

Reference yield:

: 100-15-2
N-methyl(p-nitroaniline)

: 63721-85-7
benzoic acid-(4-amino-N-methyl-anilide)

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 0 - 20 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; ethanol;
DOI:10.1021/jm3002108

Reference yield:

: 98-88-4
benzoyl chloride

: 63721-85-7
benzoic acid-(4-amino-N-methyl-anilide)

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / tetrahydrofuran / 0 - 20 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; In tetrahydrofuran; ethanol;
DOI:10.1021/jm3002108