N-(4-hydroxyphenyl)-4-methylbenzamide

Base Information

Chemical Name:N-(4-hydroxyphenyl)-4-methylbenzamide
CAS No.:23646-69-7
Molecular Formula:C14H13NO2
Molecular Weight:227.263
Hs Code.:
DSSTox Substance ID:DTXSID00400329
Wikidata:Q82203243
ChEMBL ID:CHEMBL274961
Mol file:23646-69-7.mol

Synonyms:N-(4-hydroxyphenyl)-4-methylbenzamide;23646-69-7;Oprea1_546834;Oprea1_659647;CHEMBL274961;SCHEMBL7606680;DTXSID00400329;AKOS002270538;EN300-65872;Z57160834

Suppliers and Price of N-(4-hydroxyphenyl)-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-(4-Hydroxyphenyl)-4-methylbenzamide
250mg
$ 220.00

AK Scientific
N-(4-Hydroxyphenyl)-4-methylbenzamide
2.5g
$ 664.00

AK Scientific
N-(4-Hydroxyphenyl)-4-methylbenzamide
1g
$ 387.00

Total 1 raw suppliers

Chemical Property of N-(4-hydroxyphenyl)-4-methylbenzamide

Chemical Property:

Melting Point:190 °C
Boiling Point:330.3±35.0 °C(Predicted)
PSA：52.82000
Density:1.241±0.06 g/cm3(Predicted)
LogP:3.33690
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:227.094628657
Heavy Atom Count:17
Complexity:251

Purity/Quality:: N-(4-Hydroxyphenyl)-4-methylbenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC=C(C=C1)C(=O)NC2=CC=C(C=C2)O

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

There total 10 articles about N-(4-hydroxyphenyl)-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: 89.0%

: 14235-95-1
N(hydroxy-4 phenyl) carbamate de phenyle

: 5084-80-0
tri(4-tolyl)boroxine

: 23646-69-7
N-(4-hydroxyphenyl)-4-methylbenzamide

Guidance literature:: With [Rh(OH)(cod)]2; triethylamine; In tetrahydrofuran; at 50 ℃; chemoselective reaction;
DOI:10.1021/acscatal.9b02641

Reference yield: 84.0%

: 201230-82-2
carbon monoxide

: 624-31-7
4-tolyl iodide

: 123-30-8
4-amino-phenol

: 81418-61-3
4-methyl-4-[(4-methylbenzoyl)amino]phenyl ester benzoic acid

: 23646-69-7
N-(4-hydroxyphenyl)-4-methylbenzamide

: 4-methylbenzoic acid 4-aminophenyl ester

Guidance literature:: With palladium diacetate; potassium carbonate; 1,4-di(diphenylphosphino)-butane; In acetonitrile; at 100 ℃; for 15h; under 10343.2 Torr; Reagent/catalyst; Solvent; chemoselective reaction; Autoclave; Inert atmosphere;
DOI:10.1021/ja508588b

Reference yield: 79.0%

: 23646-69-7
N-(4-hydroxyphenyl)-4-methylbenzamide

Guidance literature:: With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;