N-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide

Base Information

Chemical Name:N-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide
CAS No.:73084-05-6
Molecular Formula:C₇H₅N₃OS₂
Molecular Weight:211.268
Hs Code.:
NSC Number:291616
DSSTox Substance ID:DTXSID80315048
Wikidata:Q82067731

Synonyms:N-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide;73084-05-6;NSC 291616;NSC291616;N-(1,3,4-thiadiazol-2-yl)-2-thienylcarboxamide;DTXSID80315048;STK175592;AKOS000729482;NSC-291616;2-Thiophenecarboxamide,3,4-thiadiazole-2-yl;2-Thiophenecarboxamide,3,4-thiadiazol-2-yl-;SR-01000528985;N-(1,3,4-Thiadiazol-2-yl)-2-thiophenecarboxamide;SR-01000528985-1;N-(1,3,4-Thiadiazol-2-yl)-2-thiophenecarboxamide #;Z56874583;Thiophene-2-carboxamide, N-(1,3,4-thiadiazol-2-yl)-

Suppliers and Price of N-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide

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-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.579g/cm³
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:210.98740414
Heavy Atom Count:13
Complexity:202

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CSC(=C1)C(=O)NC2=NN=CS2

Technology Process of N-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide

There total 1 articles about N-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide 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: 94.0%

: 3437-95-4,149762-92-5
2-Iodothiophene

: 4005-51-0
[1,3,4]Thiadiazol-2-ylamin

: 124-38-9,18923-20-1
carbon dioxide

: 73084-05-6
N-(1,3,4-thiadiazol-2-yl)thiophene-2-carboxamide

Guidance literature:: With palladium diacetate; triethylamine; triphenylphosphine; In N,N-dimethyl-formamide; at 70 ℃; chemoselective reaction; Inert atmosphere; Reflux;
DOI:10.1016/j.tet.2018.03.007