Thiazolium, 4,5-dihydro-2-(3-chlorophenyl)-3-methyl-, iodide

Base Information

Chemical Name:Thiazolium, 4,5-dihydro-2-(3-chlorophenyl)-3-methyl-, iodide
CAS No.:96160-04-2
Molecular Formula:C₁₀H₁₁ClNS*I
Molecular Weight:339.628
Hs Code.:2934100090
DSSTox Substance ID:DTXSID40914632
Mol file:96160-04-2.mol

Synonyms:Thiazolium, 4,5-dihydro-2-(3-chlorophenyl)-3-methyl-, iodide;96160-04-2;4,5-Dihydro-2-(3-chlorophenyl)-3-methylthiazolium iodide;DTXSID40914632;2-(3-CHLOROPHENYL)-3-METHYL-4,5-DIHYDRO-1,3-THIAZOL-3-IUM IODIDE

Suppliers and Price of Thiazolium, 4,5-dihydro-2-(3-chlorophenyl)-3-methyl-, iodide

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
THIAZOLIUM, 4,5-DIHYDRO-2-(3-CHLOROPHENYL)-3-METHYL-, IODIDE 95.00%
5MG
$ 498.98

Total 2 raw suppliers

Chemical Property of Thiazolium, 4,5-dihydro-2-(3-chlorophenyl)-3-methyl-, iodide

Chemical Property:

PSA：28.31000
LogP:-0.56150
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:338.93455
Heavy Atom Count:14
Complexity:227

Purity/Quality:: THIAZOLIUM, 4,5-DIHYDRO-2-(3-CHLOROPHENYL)-3-METHYL-, IODIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C[N+]1=C(SCC1)C2=CC(=CC=C2)Cl.[I-]

Technology Process of Thiazolium, 4,5-dihydro-2-(3-chlorophenyl)-3-methyl-, iodide

There total 4 articles about Thiazolium, 4,5-dihydro-2-(3-chlorophenyl)-3-methyl-, iodide 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: 58.0%

: 49672-23-3
(chloro-3' phenyl)-2 Δ-2 thiazoline

: 74-88-4
methyl iodide

: 96160-04-2
2-(3-Chloro-phenyl)-3-methyl-4,5-dihydro-thiazol-3-ium; iodide

Guidance literature:: at 80 ℃; for 10h;

Reference yield:

: 587-04-2
m-Chlorobenzaldehyde

: 96160-04-2
2-(3-Chloro-phenyl)-3-methyl-4,5-dihydro-thiazol-3-ium; iodide

Guidance literature:: Multi-step reaction with 3 steps

1: 73 percent / S / dioxane / 3 h / Heating

2: 1.) P₄S₁₀; 2.) Na₂CO₃ / 1.) 150 deg C; 2.) reflux, 2 h

3: 58 percent / 10 h / 80 °C

With tetraphosphorus decasulfide; sodium carbonate; sulfur; In 1,4-dioxane;

Reference yield:

: 766-84-7
3-chloro-benzonitrile

: 96160-04-2
2-(3-Chloro-phenyl)-3-methyl-4,5-dihydro-thiazol-3-ium; iodide

Guidance literature:: Multi-step reaction with 2 steps

1: 64 percent / ethanol / 5 h / Heating

2: 58 percent / 10 h / 80 °C

In ethanol;