Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 2-(3,4,5-trimethoxyphenyl)-

Base Information

Chemical Name:Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 2-(3,4,5-trimethoxyphenyl)-
CAS No.:77803-67-9
Molecular Formula:C13H13 N3 O4 S
Molecular Weight:0
Hs Code.:2934100090
DSSTox Substance ID:DTXSID30228432
Wikidata:Q83108425
Mol file:77803-67-9.mol

Synonyms:BRN 5350364;77803-67-9;Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 2-(3,4,5-trimethoxyphenyl)-;2-(3,4,5-Trimethoxyphenyl)thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one;6-(3,4,5-Trimetossifenil)triazol(3,2-b)-s-triazol-3-(2H)-one [Italian];6-(3,4,5-Trimetossifenil)triazol(3,2-b)-s-triazol-3-(2H)-one;DTXSID30228432;LS-152245

Suppliers and Price of Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 2-(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 3 raw suppliers

Chemical Property of Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 2-(3,4,5-trimethoxyphenyl)-

Chemical Property:

Vapor Pressure:1.41E-10mmHg at 25°C
Boiling Point:511.5°C at 760 mmHg
Flash Point:263.1°C
PSA：100.77000
Density:1.49g/cm³
LogP:1.71680
XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:7
Rotatable Bond Count:4
Exact Mass:307.06267708
Heavy Atom Count:21
Complexity:386

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=NN3C(=O)CSC3=N2

Technology Process of Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 2-(3,4,5-trimethoxyphenyl)-

There total 5 articles about Thiazolo(3,2-b)(1,2,4)triazol-6(5H)-one, 2-(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: 70.0%

: 79-04-9
chloroacetyl chloride

: 14803-86-2
3-(3,4,5-trimethoxyphenyl)-4H-5-mercapto-1,2,4-triazole

: 77803-67-9
6-(3,4,5-trimetossifenil)tiazolo<3,2-b>-s-triazol-3(2H)-one

Guidance literature:: With pyridine; In benzene; for 4h; Heating;

Reference yield: 62.0%

: 77803-55-5
2-((5-(3,4,5-trimethoxyphenyl)-4H-1,2,4-triazol-3-yl)mercapto)acetic acid

: 77803-67-9
6-(3,4,5-trimetossifenil)tiazolo<3,2-b>-s-triazol-3(2H)-one

Guidance literature:: With acetic anhydride; for 2h; Heating;

Reference yield:

: 7658-75-5
1-(3,4,5-trimethoxybenzoyl)thiosemicarbazide

: 77803-67-9
6-(3,4,5-trimetossifenil)tiazolo<3,2-b>-s-triazol-3(2H)-one

Guidance literature:: Multi-step reaction with 3 steps

1: 90 percent / 5percent NaOH / H₂O / 4 h / Heating

2: 75 percent / 1/10 N NaOH / H₂O / 2 h / Heating

3: 62 percent / acetic acid anhydride / 2 h / Heating

With sodium hydroxide; acetic anhydride; In water;