N-Phenyl-2-(5-pyridin-4-yl-2H-[1,2,4]triazol-3-ylsulfanyl)-acetamide

Base Information

Chemical Name:N-Phenyl-2-(5-pyridin-4-yl-2H-[1,2,4]triazol-3-ylsulfanyl)-acetamide
CAS No.:335218-59-2
Molecular Formula:C₁₅H₁₃N₅OS
Molecular Weight:311.367
Hs Code.:
DSSTox Substance ID:DTXSID401329100
ChEMBL ID:CHEMBL1321608

Synonyms:MLS001221158;CHEMBL1321608;SCHEMBL13831257;DTXSID401329100;HMS2911C24;STK388355;AKOS000591636;AKOS005432035;N-Phenyl-2-(5-pyridin-4-yl-2H-[1,2,4]triazol-3-ylsulfanyl)-acetamide;N-phenyl-2-[(5-pyridin-4-yl-1H-1,2,4-triazol-3-yl)sulfanyl]acetamide;WAY-304871;335218-59-2;SMR000611260;SR-01000316366;SR-01000316366-1;Z17197017;N-phenyl-2-{[5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl]sulfanyl}acetamide

Suppliers and Price of N-Phenyl-2-(5-pyridin-4-yl-2H-[1,2,4]triazol-3-ylsulfanyl)-acetamide

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 0 raw suppliers

Chemical Property of N-Phenyl-2-(5-pyridin-4-yl-2H-[1,2,4]triazol-3-ylsulfanyl)-acetamide

Chemical Property:

XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:311.08408123
Heavy Atom Count:22
Complexity:358

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=O)CSC2=NNC(=N2)C3=CC=NC=C3

Technology Process of N-Phenyl-2-(5-pyridin-4-yl-2H-[1,2,4]triazol-3-ylsulfanyl)-acetamide

There total 5 articles about N-Phenyl-2-(5-pyridin-4-yl-2H-[1,2,4]triazol-3-ylsulfanyl)-acetamide 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:

: 55-22-1
pyridine-4-carboxylic acid

: 335218-59-2
N-phenyl-5-(4-pyridyl-1,3,4-triazolyl)thioacetamide

Guidance literature:: Multi-step reaction with 5 steps

1: sulfuric acid

2: hydrazine hydrate

3: potassium hydroxide

4: potassium hydroxide / Reflux

5: sodium acetate / ethanol; water / 6 h / Reflux

With sulfuric acid; sodium acetate; hydrazine hydrate; potassium hydroxide; In ethanol; water;
DOI:10.1002/cmdc.201402249

Reference yield:

: 2459-09-8
4-pyridinecarboxylic acid, methyl ester

: 335218-59-2
N-phenyl-5-(4-pyridyl-1,3,4-triazolyl)thioacetamide

Guidance literature:: Multi-step reaction with 4 steps

1: hydrazine hydrate

2: potassium hydroxide

3: potassium hydroxide / Reflux

4: sodium acetate / ethanol; water / 6 h / Reflux

With sodium acetate; hydrazine hydrate; potassium hydroxide; In ethanol; water;
DOI:10.1002/cmdc.201402249

Reference yield:

: 54-85-3,7640-37-1
isoniazid

: 335218-59-2
N-phenyl-5-(4-pyridyl-1,3,4-triazolyl)thioacetamide

Guidance literature:: Multi-step reaction with 3 steps

1: potassium hydroxide

2: potassium hydroxide / Reflux

3: sodium acetate / ethanol; water / 6 h / Reflux

With sodium acetate; potassium hydroxide; In ethanol; water;
DOI:10.1002/cmdc.201402249