N-(3-Aminophenyl)-4-methoxybenzamide

Base Information

Chemical Name:N-(3-Aminophenyl)-4-methoxybenzamide
CAS No.:41378-23-8
Molecular Formula:C₁₄H₁₄N₂O₂
Molecular Weight:242.277
Hs Code.:2924299090
DSSTox Substance ID:DTXSID80588199
Wikidata:Q82480721
Mol file:41378-23-8.mol

Synonyms:N-(3-AMINOPHENYL)-4-METHOXYBENZAMIDE;41378-23-8;CHEMBRDG-BB 4024638;SCHEMBL1337655;DTXSID80588199;MFCD08691693;AKOS000128050;BS-37679;CS-0367751

Suppliers and Price of N-(3-Aminophenyl)-4-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

Matrix Scientific
N-(3-Aminophenyl)-4-methoxybenzamide
500mg
$ 199.00

Crysdot
N-(3-Aminophenyl)-4-methoxybenzamide 95+%
5g
$ 627.00

ChemBridge Corporation
N-(3-aminophenyl)-4-methoxybenzamide 95%
5 g
$ 133.00

ChemBridge Corporation
N-(3-aminophenyl)-4-methoxybenzamide 95%
1 g
$ 46.00

American Custom Chemicals Corporation
N-(3-AMINOPHENYL)-4-METHOXYBENZAMIDE 95.00%
5MG
$ 505.99

AK Scientific
N-(3-Aminophenyl)-4-methoxybenzamide
500mg
$ 318.00

Total 7 raw suppliers

Chemical Property of N-(3-Aminophenyl)-4-methoxybenzamide

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:359.927°C at 760 mmHg
Flash Point:171.478°C
PSA：64.35000
Density:1.245g/cm³
LogP:3.18390
XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:242.105527694
Heavy Atom Count:18
Complexity:275

Purity/Quality:

98%min ^*data from raw suppliers

N-(3-Aminophenyl)-4-methoxybenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C(=O)NC2=CC=CC(=C2)N

Technology Process of N-(3-Aminophenyl)-4-methoxybenzamide

There total 1 articles about N-(3-Aminophenyl)-4-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:

: 41378-23-8
N-(3-amino-phenyl)-4-methoxy-benzamide

Guidance literature:

Reference yield:

: 98-88-4
benzoyl chloride

: 41378-23-8
N-(3-amino-phenyl)-4-methoxy-benzamide

: 625407-44-5
C₂₁H₁₈N₂O₃

Guidance literature:: With triethylamine; In acetonitrile; at 80 ℃; for 5h;
DOI:10.1016/j.bmcl.2014.06.032

Reference yield:

: 6939-63-5
(3,4,5-trimethoxy)benzoyl isothiocyanate

: 41378-23-8
N-(3-amino-phenyl)-4-methoxy-benzamide

: 1192927-84-6
3,4,5-trimethoxy-N-[(3-(4-methoxybenzoyl)aminophenylamino)carbonyl]benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: acetone / 1 h / Inert atmosphere; Reflux

2: copper(l) chloride; sodium hydroxide / acetonitrile / 0.1 h / 120 °C / 2585.81 Torr / Inert atmosphere; Microwave irradiation

With copper(l) chloride; sodium hydroxide; In acetone; acetonitrile;
DOI:10.1021/jm2013369