N-Phenylbenzimidic acid phenyl ester

Base Information

Chemical Name:N-Phenylbenzimidic acid phenyl ester
CAS No.:15940-86-0
Molecular Formula:C19H15NO
Molecular Weight:273.334
Hs Code.:2925290090
Mol file:15940-86-0.mol

Synonyms:N-Phenyl-benzimidsaeure-phenylester;N-Phenyl-benziminophenylaether;Isobenzanilid-O-phenylaether;Benzenecarboximidic acid,N-phenyl-,phenyl ester;N-phenyl-benzimidic acid phenyl ester;phenyl N-phenylbenzenecarboximidoate;

Suppliers and Price of N-Phenylbenzimidic acid phenyl ester

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

Sigma-Aldrich
N-PHENYL-BENZIMIDIC ACID PHENYL ESTER Aldrich
100mg
$ 144.00

Total 4 raw suppliers

Chemical Property of N-Phenylbenzimidic acid phenyl ester

Chemical Property:

Melting Point:105 °C
Boiling Point:403.4±28.0 °C(Predicted)
PKA:1.23±0.50(Predicted)
PSA：21.59000
Density:1.03±0.1 g/cm3(Predicted)
LogP:4.84390

Purity/Quality:

99% ^*data from raw suppliers

N-PHENYL-BENZIMIDIC ACID PHENYL ESTER Aldrich ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of N-Phenylbenzimidic acid phenyl ester

There total 9 articles about N-Phenylbenzimidic acid phenyl ester 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: 87.4%

: 4903-36-0
N-phenyl-benzimidoyl chloride

: 108-95-2,27073-41-2
phenol

: 15940-86-0
phenyl N-phenylbenzenecarboximidoate

Guidance literature:: With sodium; In 1,4-dioxane; ethanol; for 15h;
DOI:10.1134/S1070427206030190

Reference yield:

: 4903-36-0
N-phenyl-benzimidoyl chloride

: 108-95-2,27073-41-2
phenol

: 93-98-1,5705-51-1
N-phenyl benzoyl amide

: 15940-86-0
phenyl N-phenylbenzenecarboximidoate

Guidance literature:: at 150 - 160 ℃;

Reference yield:

: 93-98-1,5705-51-1
N-phenyl benzoyl amide

: 15940-86-0
phenyl N-phenylbenzenecarboximidoate

Guidance literature:: Multi-step reaction with 2 steps

1.1: thionyl chloride / Reflux

2.1: sodium / ethanol / 0.5 h

2.2: 20 °C

With thionyl chloride; sodium; In ethanol;
DOI:10.1016/j.mencom.2015.03.016