Ethyl L-thiazolidine-4-carboxylate hydrochloride

Base Information

• Chemical Name: Ethyl L-thiazolidine-4-carboxylate hydrochloride
• CAS No.: 86028-91-3
• Molecular Formula: C6H12ClNO2S
• Molecular Weight: 197.686
• Hs Code.: 2934999090
• Mol file: 86028-91-3.mol

Synonyms:4-Thiazolidinecarboxylicacid, ethyl ester, hydrochloride, (4R)- (9CI);4-Thiazolidinecarboxylic acid,ethyl ester, hydrochloride, (R)-;(4R)-Thiazolidinecarboxylic acid ethyl esterhydrochloride;Ethyl L-thiazolidine-4-carboxylate hydrochloride;

Chemical Property of Ethyl L-thiazolidine-4-carboxylate hydrochloride

Chemical Property:

• Vapor Pressure: 0.00164mmHg at 25°C
• Boiling Point: 289.7 °C at 760 mmHg
• Flash Point: 129 °C
• PSA: 63.63000
• LogP: 1.34280
• Storage Temp.: Inert atmosphere,Room Temperature

Purity/Quality:

99% ^*data from raw suppliers

EthylL-Thiazolidine-4-carboxylateHydrochloride ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

Technology Process of Ethyl L-thiazolidine-4-carboxylate hydrochloride

There total 1 articles about Ethyl L-thiazolidine-4-carboxylate hydrochloride 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:

ethanol (64-17-5) + (R)-thiazolidine-4-carboxylic acid hydrochloride (67089-84-3) → L-thiazolidine-4-carboxylic acid ethyl ester hydrochloride (86028-91-3)

Guidance literature:

With hydrogenchloride;

DOI:10.1016/0009-3084(94)90113-9

Reference yield: 96.0%

L-thiazolidine-4-carboxylic acid ethyl ester hydrochloride (86028-91-3) → ethyl (4R)-1,3-thiazolidine-4-carboxylate (60664-15-5)

Guidance literature:

With sodium carbonate;

DOI:10.1081/SCC-100103989

Reference yield: 86.0%

formaldehyd (50-00-0,30525-89-4,61233-19-0) + L-thiazolidine-4-carboxylic acid ethyl ester hydrochloride (86028-91-3) → CH2(C3H5NSCOOCH2CH3)2

Guidance literature:

With trifluoroacetic acid; at 20 ℃; for 6h;

DOI:10.1081/SCC-100103989

upstream raw materials:

ethanol

(R)-thiazolidine-4-carboxylic acid hydrochloride

Downstream raw materials:

ethyl (R)-3-methyl-1,3-thiazolidine-4-carboxylate

L-(N-hexadecanoyl)-thiazolidine-4-carboxylic acid ethyl ester

ethyl (4R)-1,3-thiazolidine-4-carboxylate

L-(N-hexadecanoyl)-thiazolidine-S-dioxide-4-carboxylic acid ethyl ester

Refernces