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Thiazolidine, hydrochloride (1:1)

Base Information Edit
  • Chemical Name:Thiazolidine, hydrochloride (1:1)
  • CAS No.:14446-47-0
  • Molecular Formula:C3H7NS.ClH
  • Molecular Weight:125.622
  • Hs Code.:2934999090
  • Mol file:14446-47-0.mol
Thiazolidine, hydrochloride (1:1)

Synonyms:thiazolidine, hydrochloride;thiazolidinium chloride;Thiazolidin, Hydrochlorid;

Suppliers and Price of Thiazolidine, hydrochloride (1:1)
Supply Marketing:Edit
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
  • TRC
  • ThiazolidineHydrochloride
  • 500mg
  • $ 75.00
  • SynQuest Laboratories
  • Thiazolidinehydrochloride 95%
  • 25 g
  • $ 512.00
  • SynQuest Laboratories
  • Thiazolidinehydrochloride 95%
  • 5 g
  • $ 184.00
  • Crysdot
  • Thiazolidinehydrochloride 97%
  • 100g
  • $ 131.00
  • Chemenu
  • ThiazolidineHydrochloride 97%
  • 100g
  • $ 107.00
  • Ark Pharm
  • Thiazolidine hydrochloride 97%
  • 25g
  • $ 31.00
  • Ark Pharm
  • Thiazolidine hydrochloride 97%
  • 10g
  • $ 15.00
  • Ark Pharm
  • Thiazolidine hydrochloride 97%
  • 5g
  • $ 9.00
  • Ark Pharm
  • Thiazolidine hydrochloride 97%
  • 100g
  • $ 96.00
  • Ark Pharm
  • Thiazolidine hydrochloride 97%
  • 500g
  • $ 353.00
Total 45 raw suppliers
Chemical Property of Thiazolidine, hydrochloride (1:1) Edit
Chemical Property:
  • Melting Point:180 °C(Solv: water (7732-18-5)) 
  • PSA:37.33000 
  • LogP:1.41110 
Purity/Quality:

97% *data from raw suppliers

ThiazolidineHydrochloride *data from reagent suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
Technology Process of Thiazolidine, hydrochloride (1:1)

There total 1 articles about Thiazolidine, hydrochloride (1:1) 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:
Guidance literature:
N-tert-butoxycarbonyl-4-oxo-L-proline; With triethylamine; In dichloromethane; at -5 - 5 ℃; for 0.5h;
thiazolidine hydrochloride; With pivaloyl chloride; triethylamine; In dichloromethane; at -5 - 5 ℃; for 4h;
Guidance literature:
With lithium aluminium tetrahydride; In tetrahydrofuran; for 2h; Inert atmosphere; Reflux;
DOI:10.1016/j.bbrc.2010.11.052
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