2-Thiophenecarboxamide, N-(3-chlorophenyl)-

Base Information

Chemical Name:2-Thiophenecarboxamide, N-(3-chlorophenyl)-
CAS No.:79822-82-5
Molecular Formula:C11H8ClNOS
Molecular Weight:237.71
Hs Code.:
Mol file:79822-82-5.mol

Synonyms:3'-chloro-2-thiophenecarboxanilide;thiophene-2-carboxylic acid-(3-chloro-anilide);Thiophen-2-carbonsaeure-(3-chlor-anilid);Thiophene-2-carboxylic acid (3-chloro-phenyl)-amide;

Suppliers and Price of 2-Thiophenecarboxamide, N-(3-chlorophenyl)-

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

American Custom Chemicals Corporation
N-(3-CHLOROPHENYL)-2-THIOPHENECARBOXAMIDE 95.00%
5MG
$ 500.93

Total 0 raw suppliers

Chemical Property of 2-Thiophenecarboxamide, N-(3-chlorophenyl)-

Chemical Property:

Melting Point:139 - 140 °C
PSA：57.34000
LogP:3.72680

Purity/Quality:: N-(3-CHLOROPHENYL)-2-THIOPHENECARBOXAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-Thiophenecarboxamide, N-(3-chlorophenyl)-

There total 3 articles about 2-Thiophenecarboxamide, N-(3-chlorophenyl)- 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:

: 5271-67-0
2-Thiophenecarbonyl chloride

: 108-42-9
3-chloro-aniline

: 79822-82-5
N-(3-chlorophenyl)thiophene-2-carboxamide

Guidance literature:: With pyridine;

Reference yield:

: 527-72-0
2-thiophenylcarboxylic acid

: 79822-82-5
N-(3-chlorophenyl)thiophene-2-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 0.5 h / Heating

2: triethylamine / CH₂Cl₂ / 1 h / Heating

With thionyl chloride; triethylamine; In dichloromethane;
DOI:10.1002/jhet.5570390616