N-(3-hydroxy-1,2,4-thiadiazol-5-yl)benzenecarboxamide

Base Information

Chemical Name:N-(3-hydroxy-1,2,4-thiadiazol-5-yl)benzenecarboxamide
CAS No.:69775-48-0
Molecular Formula:C9H7N3O2S
Molecular Weight:221.239
Hs Code.:
ChEMBL ID:CHEMBL259516
DSSTox Substance ID:DTXSID30404193
Nikkaji Number:J432.402A
Wikidata:Q82208238

Synonyms:69775-48-0;N-(3-hydroxy-1,2,4-thiadiazol-5-yl)benzenecarboxamide;N-(3-oxo-1,2,4-thiadiazol-5-yl)benzamide;N-(3-Oxo-2,3-dihydro-1,2,4-thiadiazol-5-yl)benzamide;MLS000736063;3M-519S;SMR000338613;N-(3-Hydroxy-1,2,4-thiadiazol-5-yl)benzamide;CHEMBL259516;BDBM60185;cid_4553009;DTXSID30404193;HMS2647O15;MFCD04125105;AKOS005088597;AKOS030240369;N-(3-keto-1,2,4-thiadiazol-5-yl)benzamide;SR-01000309106;SR-01000309106-1;N-(3-oxidanylidene-1,2,4-thiadiazol-5-yl)benzamide

Suppliers and Price of N-(3-hydroxy-1,2,4-thiadiazol-5-yl)benzenecarboxamide

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 3 raw suppliers

Chemical Property of N-(3-hydroxy-1,2,4-thiadiazol-5-yl)benzenecarboxamide

Chemical Property:

XLogP3:1.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:221.02589765
Heavy Atom Count:15
Complexity:311

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC2=NC(=O)NS2

Technology Process of N-(3-hydroxy-1,2,4-thiadiazol-5-yl)benzenecarboxamide

There total 4 articles about N-(3-hydroxy-1,2,4-thiadiazol-5-yl)benzenecarboxamide 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: 76.0%

: 34277-78-6
N-(carbamoylcarbamothioyl)benzamide

: 69775-48-0
N-(3-oxo-2,3-dihydro-1,2,4-thiadiazol-5-yl)benzamide

Guidance literature:: With N-Bromosuccinimide; In methanol; for 12h; Heating;
DOI:10.1016/j.bmc.2008.04.036

Reference yield:

: 98-88-4
benzoyl chloride

: 69775-48-0
N-(3-oxo-2,3-dihydro-1,2,4-thiadiazol-5-yl)benzamide

Guidance literature:: Multi-step reaction with 3 steps

1: acetone / 3.5 h / 50 °C

2: acetone / 5 h

3: N-Bromosuccinimide / methanol / 70 °C

With N-Bromosuccinimide; In methanol; acetone;
DOI:10.1016/j.bmc.2021.115998