Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide

Base Information

Chemical Name:Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide
CAS No.:17091-45-1
Molecular Formula:Br*C₁₂H₁₄NS
Molecular Weight:284.22
Hs Code.:2934100090
DSSTox Substance ID:DTXSID10884959
Mol file:17091-45-1.mol

Synonyms:17091-45-1;3-benzyl-2,4-dimethyl-1,3-thiazol-3-ium bromide;Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide;2,4-Dimethyl-3-benzyl-thiazolium bromide;3-benzyl-2,4-dimethyl-1,3-thiazol-3-ium;bromide;Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide (1:1);Cromolynsodium;C12H14NS.Br;C12-H14-N-S.Br;DTXSID10884959;3-Benzyl-2,4-dimethylthiazol-3-ium bromide;FT-0696645;Thiazolium,2,4-dimethyl-3-(phenylmethyl)-,bromide(1:1)

Suppliers and Price of Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide

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
3-BENZYL-2,4-DIMETHYL-1,3-THIAZOL-3-IUM BROMIDE 95.00%
5MG
$ 500.95

Total 8 raw suppliers

Chemical Property of Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide

Chemical Property:

Melting Point:171 °C(Solv: ethanol (64-17-5); ethyl ether (60-29-7))
Boiling Point:°Cat760mmHg
Flash Point:°C
PSA：32.12000
Density:g/cm³
LogP:-0.29530
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:283.00303
Heavy Atom Count:15
Complexity:177

Purity/Quality:

99% ^*data from raw suppliers

3-BENZYL-2,4-DIMETHYL-1,3-THIAZOL-3-IUM BROMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=CSC(=[N+]1CC2=CC=CC=C2)C.[Br-]

Technology Process of Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide

There total 1 articles about Thiazolium, 2,4-dimethyl-3-(phenylmethyl)-, bromide 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: