N-(2-aminophenyl)-4-methylbenzamide

Base Information

Chemical Name:N-(2-aminophenyl)-4-methylbenzamide
CAS No.:71255-53-3
Molecular Formula:C14H14N2O
Molecular Weight:226.278
Hs Code.:2924299090
DSSTox Substance ID:DTXSID30401006
Wikidata:Q82204073
Mol file:71255-53-3.mol

Synonyms:N-(2-aminophenyl)-4-methylbenzamide;71255-53-3;Oprea1_673036;SCHEMBL8242923;DTXSID30401006;NSC773316;AKOS000128641;NSC-773316;CS-0246109;EU-0000088;EN300-31746;SR-01000389423;SR-01000389423-1;Z239120464

Suppliers and Price of N-(2-aminophenyl)-4-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

TRC
N-(2-Aminophenyl)-4-methylbenzamide
250mg
$ 265.00

American Custom Chemicals Corporation
N-(2-AMINOPHENYL)-4-METHYLBENZAMIDE 95.00%
5G
$ 1421.65

American Custom Chemicals Corporation
N-(2-AMINOPHENYL)-4-METHYLBENZAMIDE 95.00%
2.5G
$ 1147.43

American Custom Chemicals Corporation
N-(2-AMINOPHENYL)-4-METHYLBENZAMIDE 95.00%
1G
$ 808.89

AK Scientific
N-(2-Aminophenyl)-4-methylbenzamide
100mg
$ 189.00

AK Scientific
N-(2-Aminophenyl)-4-methylbenzamide
1g
$ 445.00

AK Scientific
N-(2-Aminophenyl)-4-methylbenzamide
500mg
$ 334.00

Total 3 raw suppliers

Chemical Property of N-(2-aminophenyl)-4-methylbenzamide

Chemical Property:

Boiling Point:321.6±35.0 °C(Predicted)
PKA:13.37±0.70(Predicted)
PSA：55.12000
Density:1.210±0.06 g/cm3(Predicted)
LogP:3.48370
XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:226.110613074
Heavy Atom Count:17
Complexity:259

Purity/Quality:

98%Min ^*data from raw suppliers

N-(2-Aminophenyl)-4-methylbenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=O)NC2=CC=CC=C2N
Uses N-(2-aminophenyl)-4-methylbenzamide is used in biological studies for chemoproteomics profiling of HDAC inhibitors reveals selective targeting of HDAC complexes.

Technology Process of N-(2-aminophenyl)-4-methylbenzamide

There total 6 articles about N-(2-aminophenyl)-4-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: 88.0%

: 349089-26-5
N-(2-iodophenyl)-4-methyl-benzamide

: 71255-53-3
2'-amino-4-methylbenzanilide

Guidance literature:: With ammonium hydroxide; potassium phosphate; copper(II) bis(trifluoromethanesulfonate); vasicine; In ethanol; at 70 ℃; for 12h; regioselective reaction; Sealed tube;
DOI:10.1016/j.tetlet.2021.153001

Reference yield: 84.0%

: 346720-06-7
N-(2-bromophenyl)-4-methylbenzamide

: 71255-53-3
2'-amino-4-methylbenzanilide

Guidance literature:: With ammonium hydroxide; potassium phosphate; copper(II) bis(trifluoromethanesulfonate); vasicine; In ethanol; at 70 ℃; for 12h; regioselective reaction; Sealed tube;
DOI:10.1016/j.tetlet.2021.153001