3-Chloro-4-methoxy-1,2,5-thiadiazole

Base Information

Chemical Name:3-Chloro-4-methoxy-1,2,5-thiadiazole
CAS No.:5728-16-5
Molecular Formula:C3H3ClN2OS
Molecular Weight:150.589
Hs Code.:
European Community (EC) Number:944-002-8
DSSTox Substance ID:DTXSID50592586
Wikidata:Q82486768
Mol file:5728-16-5.mol

Synonyms:3-CHLORO-4-METHOXY-1,2,5-THIADIAZOLE;5728-16-5;3-methoxy-4-chloro-1,2,5-thiadiazole;SCHEMBL4030569;DTXSID50592586;SNLDYFHPRJMKLQ-UHFFFAOYSA-N;4-chloro-3-methoxy-1,2,5-thiadiazole

Suppliers and Price of 3-Chloro-4-methoxy-1,2,5-thiadiazole

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

TRC
3-Chloro-4-methoxy-1,2,5-thiadiazole
10g
$ 1320.00

Total 5 raw suppliers

Chemical Property of 3-Chloro-4-methoxy-1,2,5-thiadiazole

Chemical Property:

PSA：63.25000
LogP:1.20010
XLogP3:1.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:149.9654616
Heavy Atom Count:8
Complexity:83.7

Purity/Quality:

99% ^*data from raw suppliers

3-Chloro-4-methoxy-1,2,5-thiadiazole ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=NSN=C1Cl
Uses 3-Chloro-4-methoxy-1,2,5-thiadiazole has been used as a reactant for the preparation of selective ligands at human 5-HT1A receptors.

Technology Process of 3-Chloro-4-methoxy-1,2,5-thiadiazole

There total 4 articles about 3-Chloro-4-methoxy-1,2,5-thiadiazole 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: 27.0%

: 124-41-4
sodium methylate

: 5728-20-1
3,4-dichloro-1,2,5-thiadiazole

: 5728-16-5
3-methoxy-4-chloro-1,2,5-thiadiazole

Guidance literature:: In methanol; Heating;
DOI:10.1016/S0960-894X(01)00151-2

Reference yield: 10.1%

: 67-56-1
methanol

: 5728-20-1
3,4-dichloro-1,2,5-thiadiazole

: 5728-16-5
3-methoxy-4-chloro-1,2,5-thiadiazole

Guidance literature:: methanol; With sodium hydride; for 1h; Heating;

3,4-dichloro-1,2,5-thiadiazole; In tetrahydrofuran; methanol; at 20 ℃; for 24h;
DOI:10.1021/jm0301235