2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-N-(3-chlorophenyl)acetamide

Base Information

Chemical Name:2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-N-(3-chlorophenyl)acetamide
CAS No.:502998-40-5
Molecular Formula:C₁₀H₉ClN₄OS₂
Molecular Weight:300.793
Hs Code.:
DSSTox Substance ID:DTXSID101329199
ChEMBL ID:CHEMBL1512445
Mol file:502998-40-5.mol

Synonyms:2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-N-(3-chlorophenyl)acetamide;2-((5-amino-1,3,4-thiadiazol-2-yl)thio)-N-(3-chlorophenyl)acetamide;502998-40-5;Oprea1_442646;Oprea1_814908;MLS002164766;CHEMBL1512445;DTXSID101329199;HMS3026H06;AKOS000112119;SMR001247137;CS-0306150;AN-919/41439974;Z18452832;2-(5-amino-1,3,4-thiadiazol-2-ylthio)-N-(3-chlorophenyl)acetamide;2-(5-amino-1,3,4-thiadi azol-2-ylthio)-N-(3-chlo rophenyl)acetamide;n-(3-Chlorophenyl)-2-((5-imino-4,5-dihydro-1,3,4-thiadiazol-2-yl)thio)acetamide

Suppliers and Price of 2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-N-(3-chlorophenyl)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

American Custom Chemicals Corporation
2-[(5-AMINO-1,3,4-THIADIAZOL-2-YL)SULFANYL]-N-(3-CHLOROPHENYL)ACETAMIDE 95.00%
5MG
$ 496.31

Total 0 raw suppliers

Chemical Property of 2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-N-(3-chlorophenyl)acetamide

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:299.9906310
Heavy Atom Count:18
Complexity:297

Purity/Quality:: 2-[(5-AMINO-1,3,4-THIADIAZOL-2-YL)SULFANYL]-N-(3-CHLOROPHENYL)ACETAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Cl)NC(=O)CSC2=NN=C(S2)N

Technology Process of 2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-N-(3-chlorophenyl)acetamide

There total 2 articles about 2-[(5-amino-1,3,4-thiadiazol-2-yl)sulfanyl]-N-(3-chlorophenyl)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: 86.0%

: 2564-05-8
2-chloro-N-(3-chlorophenyl)acetamide

: 2349-67-9
2-Amino-5-mercapto-1,3,4-thiadiazole

: 502998-40-5
2-((5-amino-1,3,4-thiadiazol-2-yl)thio)-N-(3-chlorophenyl)acetamide

Guidance literature:: With sodium hydroxide; In ethanol; water; at 20 ℃;
DOI:10.2174/1573406412666160201120806

Reference yield:

: 108-42-9
3-chloro-aniline

: 502998-40-5
2-((5-amino-1,3,4-thiadiazol-2-yl)thio)-N-(3-chlorophenyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dichloromethane

2: sodium hydroxide / ethanol; water / 20 °C

With potassium carbonate; sodium hydroxide; In ethanol; dichloromethane; water;
DOI:10.2174/1573406412666160201120806