Thiazole, 4,5-dihydro-2,4,4-trimethyl-

Base Information

Chemical Name:Thiazole, 4,5-dihydro-2,4,4-trimethyl-
CAS No.:4145-94-2
Molecular Formula:C6H11NS
Molecular Weight:129.2232
Hs Code.:
DSSTox Substance ID:DTXSID20194359
Nikkaji Number:J2.109.307F
Wikipedia:Trimethylthiazoline
Wikidata:Q83067120
Mol file:4145-94-2.mol

Synonyms:Thiazole, 4,5-dihydro-2,4,4-trimethyl-;BRN 0107669;4145-94-2;4,5-Dihydro-2,4,4-trimethylthiazole;trimethylthiazoline;2,4,4-Trimethyl-2-thiazoline;SCHEMBL13278423;DTXSID20194359;2,4,4-Trimethyl-delta2-thiazoline;2,4,4-Trimethyl-delta^2-thiazoline;AKOS024366474;2,4,4-Trimethyl-4,5-dihydrothiazole;LS-150968;4-27-00-00931 (Beilstein Handbook Reference)

Suppliers and Price of Thiazole, 4,5-dihydro-2,4,4-trimethyl-

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 6 raw suppliers

Chemical Property of Thiazole, 4,5-dihydro-2,4,4-trimethyl-

Chemical Property:

Vapor Pressure:5.71mmHg at 25°C
Boiling Point:147°C at 760 mmHg
Flash Point:47.2°C
Density:1.05g/cm³
XLogP3:0.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:129.06122053
Heavy Atom Count:8
Complexity:127

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=NC(CS1)(C)C

Technology Process of Thiazole, 4,5-dihydro-2,4,4-trimethyl-

There total 7 articles about Thiazole, 4,5-dihydro-2,4,4-trimethyl- 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: 50.0%

: 1569-96-6
N-(1-hydroxy-2-methylpropan-2-yl)acetamide

: 4145-94-2
2,4,4-trimethylthiazolidine

Guidance literature:: With tetraphosphorus decasulfide; at 120 - 130 ℃; for 1.5h; suspension in mineral acid;

Reference yield:

: 124-68-5
2-Amino-2-methyl-1-propanol

: 75-36-5
acetyl chloride

: 4145-94-2
2,4,4-trimethylthiazolidine

Guidance literature:: 2-Amino-2-methyl-1-propanol; acetyl chloride; With triethylamine; In dichloromethane; at 0 ℃; for 0.5h;

With Lawessons reagent; In toluene; for 0.25h; Further stages.; Heating;
DOI:10.1016/j.tetlet.2004.09.182