2-(2-Amino[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol

Base Information

Chemical Name:2-(2-Amino[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol
CAS No.:137609-25-7
Molecular Formula:C₁₀H₉N₃OS₂
Molecular Weight:251.333
Hs Code.:
DSSTox Substance ID:DTXSID201194658

Synonyms:137609-25-7;2-(2-amino-5H-thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol;2-(2-amino[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol;2-(2-amino-5H-[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol;2-{2-AMINO-5H-[1,3]THIAZOLO[4,3-B][1,3,4]THIADIAZOL-5-YL}PHENOL;starbld0037647;2-(2-Amino[1,3]thiazolo[4,3-b]-[1,3,4]thiadiazol-5-yl)phenol;DTXSID201194658;AKOS015960037;VS-09122;2-(2-Amino-5H-thiazolo[4,3-b]-1,3,4-thiadiazol-5-yl)phenol

Suppliers and Price of 2-(2-Amino[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol

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-(2-AMINO[1,3]THIAZOLO[4,3-B][1,3,4]THIADIAZOL-5-YL)PHENOL 95.00%
5MG
$ 504.26

Total 2 raw suppliers

Chemical Property of 2-(2-Amino[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol

Chemical Property:

XLogP3:2.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:1
Exact Mass:251.01870427
Heavy Atom Count:16
Complexity:358

Purity/Quality:

98%min ^*data from raw suppliers

2-(2-AMINO[1,3]THIAZOLO[4,3-B][1,3,4]THIADIAZOL-5-YL)PHENOL 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C2N3C(=CS2)SC(=N3)N)O

Technology Process of 2-(2-Amino[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol

There total 2 articles about 2-(2-Amino[1,3]thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)phenol 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: 72.0%

: 137609-06-4
[2-(2-Hydroxy-phenyl)-4-oxo-thiazolidin-3-yl]-thiourea

: 137609-25-7
2-(2-Amino-thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)-phenol

Guidance literature:: With sulfuric acid;

Reference yield:

: 5351-90-6,17149-00-7
salicylaldehyde thiosemicarbazone

: 137609-25-7
2-(2-Amino-thiazolo[4,3-b][1,3,4]thiadiazol-5-yl)-phenol

Guidance literature:: Multi-step reaction with 2 steps

1: 70.3 percent / dioxane / Heating

2: 72 percent / conc. H₂SO₄

With sulfuric acid; In 1,4-dioxane;