n-(2-Hydroxyphenyl)-n-methylbenzamide

Base Information

Chemical Name:n-(2-Hydroxyphenyl)-n-methylbenzamide
CAS No.:3743-16-6
Molecular Formula:C14H13NO2
Molecular Weight:227.2585
Hs Code.:
NSC Number:86997
DSSTox Substance ID:DTXSID20293053
Nikkaji Number:J3.311.379J
Wikidata:Q82031621

Synonyms:n-(2-hydroxyphenyl)-n-methylbenzamide;3743-16-6;NSC86997;NCIOpen2_005161;SCHEMBL8812454;DTXSID20293053;NSC-86997

Suppliers and Price of n-(2-Hydroxyphenyl)-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 5 raw suppliers

Chemical Property of n-(2-Hydroxyphenyl)-n-methylbenzamide

Chemical Property:

Vapor Pressure:3.14E-06mmHg at 25°C
Boiling Point:377.3°C at 760 mmHg
Flash Point:182°C
Density:1.226g/cm³
XLogP3:2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:227.094628657
Heavy Atom Count:17
Complexity:261

Purity/Quality:: 95% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(C1=CC=CC=C1O)C(=O)C2=CC=CC=C2

Technology Process of n-(2-Hydroxyphenyl)-n-methylbenzamide

There total 5 articles about n-(2-Hydroxyphenyl)-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: 62.0%

: 100-61-8
N-methylaniline

: 94-36-0
dibenzoyl peroxide

: 3743-16-6
benzoic acid-(2-hydroxy-N-methyl-anilide)

Guidance literature:: With sodium acetate; at 80 ℃; for 20h; Reagent/catalyst;
DOI:10.1021/ol501293c

Reference yield: 61.0%

: 1934-92-5
N-methyl-N-phenyl-benzamide

: 3743-16-6
benzoic acid-(2-hydroxy-N-methyl-anilide)

Guidance literature:: With dipotassium peroxodisulfate; palladium diacetate; trifluoroacetic acid; trifluoroacetic anhydride; at 60 ℃; for 1.5h; Reagent/catalyst; regioselective reaction; Mechanism;
DOI:10.1039/c5sc03905c