Benzamide, N-[2-(propylthio)phenyl]-

Base Information

Chemical Name:Benzamide, N-[2-(propylthio)phenyl]-
CAS No.:73153-65-8
Molecular Formula:C16H17NOS
Molecular Weight:271.383
Hs Code.:

Synonyms:Benzoesaeure-(2-propylmercapto-anilid);2-Benzamidophenyl-propyl-sulfid;N-[2-(propylthio)phenyl]benzamide;benzoic acid-(2-propylsulfanyl-anilide);Benzamide,N-[2-(propylthio)phenyl];

Suppliers and Price of Benzamide, N-[2-(propylthio)phenyl]-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of Benzamide, N-[2-(propylthio)phenyl]-

Chemical Property:

PSA：57.89000
LogP:4.82500

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Benzamide, N-[2-(propylthio)phenyl]-

There total 6 articles about Benzamide, N-[2-(propylthio)phenyl]- 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: 98.0%

: 79792-95-3
2-(propylthio)aniline

: 98-88-4
benzoyl chloride

: 73153-65-8
N-[2-(propylthio)phenyl]benzamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1021/jo035835h

Reference yield:

: 76697-38-6
1-propylsulfanyl-2-nitrobenzene

: 73153-65-8
N-[2-(propylthio)phenyl]benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 74 percent / iron; AcOH / H₂O / 0.5 h / 100 °C

2: 98 percent / triethylamine / CH₂Cl₂ / 1 h / 20 °C

With iron; acetic acid; triethylamine; In dichloromethane; water;
DOI:10.1021/jo035835h

Reference yield:

: 88-73-3
2-Chloronitrobenzene

: 73153-65-8
N-[2-(propylthio)phenyl]benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: 96 percent / NaOH / ethanol / 2 h / 20 °C

2: 74 percent / iron; AcOH / H₂O / 0.5 h / 100 °C

3: 98 percent / triethylamine / CH₂Cl₂ / 1 h / 20 °C

With sodium hydroxide; iron; acetic acid; triethylamine; In ethanol; dichloromethane; water;
DOI:10.1021/jo035835h