86028-91-3

  • Product NameEthyl L-thiazolidine-4-carboxylate hydrochloride
  • Molecular FormulaC6H12ClNO2S
  • Molecular Weight197.686
  • Purity99%
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Product Details

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  • CasNo: 86028-91-3
  • Molecular Formula: C6H12ClNO2S
  • Purity: 99%

Export High Quality Ethyl L-thiazolidine-4-carboxylate hydrochloride 86028-91-3

  • Molecular Formula:C6H12ClNO2S
  • Molecular Weight:197.686
  • 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 

Ethyl L-thiazolidine-4-carboxylate hydrochloride(Cas 86028-91-3) Usage

(R)-Ethyl thiazolidine-4-carboxylate hydrochloride is an activating reagent that can be used in the synthesis of a variety of organic compounds. The product is for non-human research only. Not for therapeutic or veterinary use.

InChI:InChI=1/C6H11NO2S.ClH/c1-2-9-6(8)5-3-10-4-7-5;/h5,7H,2-4H2,1H3;1H

86028-91-3 Relevant articles

Solubility Behavior of Ethyl l-Thiazolidine-4-carboxylate Hydrochloride in 15 Neat Solvents and Ethanol + Methyl Acetate Binary Solvent from 283.15 to 323.15 K

Jingxuan Qiu, Peng Wang*, Shen Hu, Hui He, Haishuang Huang, Yue Zhao, Jiaming Han, Haoyou Liu, and Ying Guo

J. Chem. Eng. Data 2021, 66, 4, 1821–1830

The solid phase of ethyl l-thiazolidine-4-carboxylate hydrochloride in the investigated solvent systems was characterized by the powder X-ray diffraction test.

Synthesis of the new immunostimulating agent pidotimod (3‐L‐pyroglutamyl‐L‐thiazolidine‐4‐carboxylic acid) labelled with 14C‐ and 35S‐isotopes

Patrizia Ferraboschi, Paride Grisenti, Enzo Santaniello, Claudio Giachetti, Giovanni Zanolo, Giovanni Signorelli, Germano Coppi

Journal of Labelled Compounds and Radiopharmaceuticals, Volume31, Issue12 December 1992 Pages 973-980

Biological response modifiers have a rationale for use in … For the preparative use, 50 mg of labelled Pidotimod 1 was … unlabelled ethyl L-thiazolidine-4-carboxylate 3 and the ethyl ester 4 …

86028-91-3 Process route

ethanol
64-17-5

ethanol

(R)-thiazolidine-4-carboxylic acid hydrochloride
67089-84-3

(R)-thiazolidine-4-carboxylic acid hydrochloride

L-thiazolidine-4-carboxylic acid ethyl ester hydrochloride
86028-91-3

L-thiazolidine-4-carboxylic acid ethyl ester hydrochloride

Conditions
Conditions Yield
With hydrogenchloride;
 
L-thiazolidine-4-carboxylic acid ethyl ester hydrochloride
86028-91-3

L-thiazolidine-4-carboxylic acid ethyl ester hydrochloride

ethyl (4R)-1,3-thiazolidine-4-carboxylate
60664-15-5

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

Conditions
Conditions Yield
With sodium carbonate;
96%

86028-91-3 Upstream products

  • 64-17-5
    64-17-5

    ethanol

  • 67089-84-3
    67089-84-3

    (R)-thiazolidine-4-carboxylic acid hydrochloride

86028-91-3 Downstream products

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

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    161859-44-5

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

  • 60664-15-5
    60664-15-5

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

  • 161859-48-9
    161859-48-9

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

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