Thiazolo(2,3-c)-1,2,4-triazole, 5-phenyl-3-(3,4,5-trimethoxyphenyl)-

Base Information

Chemical Name:Thiazolo(2,3-c)-1,2,4-triazole, 5-phenyl-3-(3,4,5-trimethoxyphenyl)-
CAS No.:140423-93-4
Molecular Formula:C19H17 N3 O3 S
Molecular Weight:367.4216
Hs Code.:
DSSTox Substance ID:DTXSID60161383
Nikkaji Number:J455.230J
Wikidata:Q83029781

Synonyms:BRN 4885016;140423-93-4;Thiazolo(2,3-c)-1,2,4-triazole, 5-phenyl-3-(3,4,5-trimethoxyphenyl)-;5-Phenyl-3-(3,4,5-trimethoxyphenyl)thiazolo(2,3-c)-1,2,4-triazole;DTXSID60161383;LS-152228;3-(3,4,5-Trimethoxyphenyl)-5-(phenyl)thiazolo[2,3-c]-1,2,4-triazole

Suppliers and Price of Thiazolo(2,3-c)-1,2,4-triazole, 5-phenyl-3-(3,4,5-trimethoxyphenyl)-

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 4 raw suppliers

Chemical Property of Thiazolo(2,3-c)-1,2,4-triazole, 5-phenyl-3-(3,4,5-trimethoxyphenyl)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.33g/cm³
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:367.09906259
Heavy Atom Count:26
Complexity:451

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OC)OC)C2=NN=C3N2C(=CS3)C4=CC=CC=C4

Technology Process of Thiazolo(2,3-c)-1,2,4-triazole, 5-phenyl-3-(3,4,5-trimethoxyphenyl)-

There total 4 articles about Thiazolo(2,3-c)-1,2,4-triazole, 5-phenyl-3-(3,4,5-trimethoxyphenyl)- 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: 78.0%

: 140405-96-5
1-Phenyl-2-[5-(3,4,5-trimethoxy-phenyl)-4H-[1,2,4]triazol-3-ylsulfanyl]-ethanone

: 140423-93-4
5-Phenyl-3-(3,4,5-trimethoxy-phenyl)-thiazolo[2,3-c][1,2,4]triazole

Guidance literature:: With trichlorophosphate; In xylene; Heating;
DOI:10.1016/0223-5234(91)90135-A

Reference yield:

: 77803-52-2
2-<2-(3,4,5-trimetossibenzoil)>idrazino-4-feniltiazolo

: 140423-93-4
5-Phenyl-3-(3,4,5-trimethoxy-phenyl)-thiazolo[2,3-c][1,2,4]triazole

Guidance literature:: With trichlorophosphate; at 120 - 130 ℃; for 3h;
DOI:10.1016/0223-5234(91)90135-A

Reference yield:

: 70-11-1
α-bromoacetophenone

: 140423-93-4
5-Phenyl-3-(3,4,5-trimethoxy-phenyl)-thiazolo[2,3-c][1,2,4]triazole

Guidance literature:: Multi-step reaction with 2 steps

1: 85 percent / KOH, MeOH / 0.5 h / Heating

2: 78 percent / POCl₃ / xylene / Heating

With methanol; potassium hydroxide; trichlorophosphate; In xylene;
DOI:10.1016/0223-5234(91)90135-A