3-amino-N-(4-chlorophenyl)benzamide

Base Information

Chemical Name:3-amino-N-(4-chlorophenyl)benzamide
CAS No.:115175-17-2
Molecular Formula:C13H11ClN2O
Molecular Weight:246.696
Hs Code.:2924299090
DSSTox Substance ID:DTXSID00588393
Wikidata:Q82481042
Mol file:115175-17-2.mol

Synonyms:3-amino-N-(4-chlorophenyl)benzamide;115175-17-2;Benzamide, 3-amino-N-(4-chlorophenyl)-;3-AMINO-N-(4-CHLOROPHENYL)BENZAMIDE 95%;SCHEMBL1355088;DTXSID00588393;PFLYFNYASPUBRC-UHFFFAOYSA-N;MFCD01112158;STK360037;AKOS000136475;MCULE-1406695793;3-amino-N-(4-chloro-phenyl)-benzamide;BS-35636

Suppliers and Price of 3-amino-N-(4-chlorophenyl)benzamide

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

TRC
3-Amino-N-(4-chlorophenyl)benzamide
100mg
$ 75.00

Matrix Scientific
3-Amino-N-(4-chlorophenyl)benzamide
500mg
$ 199.00

Crysdot
3-Amino-N-(4-chlorophenyl)benzamide 95+%
5g
$ 627.00

ChemBridge Corporation
3-amino-N-(4-chlorophenyl)benzamide 95%
1 g
$ 46.00

American Custom Chemicals Corporation
3-AMINO-N-(4-CHLOROPHENYL)BENZAMIDE 95.00%
500MG
$ 795.80

AK Scientific
3-Amino-N-(4-chlorophenyl)benzamide
500mg
$ 318.00

Total 7 raw suppliers

Chemical Property of 3-amino-N-(4-chlorophenyl)benzamide

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:351.271°C at 760 mmHg
Flash Point:166.243°C
PSA：55.12000
Density:1.351g/cm³
LogP:3.82870
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:246.0559907
Heavy Atom Count:17
Complexity:264

Purity/Quality:

97% ^*data from raw suppliers

3-Amino-N-(4-chlorophenyl)benzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 3-amino-N-(4-chlorophenyl)benzamide

There total 3 articles about 3-amino-N-(4-chlorophenyl)benzamide 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: 97.0%

: 99514-24-6
N-(4-chloro-phenyl)-3-nitro-benzamide

: 115175-17-2
3-amino-N-(4-chloro-phenyl)-benzamide

Guidance literature:: With iron; ammonium chloride; In methanol; for 7h; Reflux;
DOI:10.3390/molecules21050676

Reference yield:

: 121-92-6
3-nitrobenzoic acid

: 115175-17-2
3-amino-N-(4-chloro-phenyl)-benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: oxalyl dichloride; triethylamine / benzene / 1 h / Reflux

2: triethylamine / benzene / 3 h / 20 °C

3: ammonium chloride; iron / methanol / 7 h / Reflux

With oxalyl dichloride; iron; ammonium chloride; triethylamine; In methanol; benzene;
DOI:10.3390/molecules21050676

Reference yield:

: 121-90-4
m-nitrobenzoic acid chloride

: 115175-17-2
3-amino-N-(4-chloro-phenyl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / benzene / 3 h / 20 °C

2: ammonium chloride; iron / methanol / 7 h / Reflux

With iron; ammonium chloride; triethylamine; In methanol; benzene;
DOI:10.3390/molecules21050676