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Ethyl L-thiazolidine-4-carboxylate hydrochloride

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Ethyl L-thiazolidine-4-carboxylate hydrochloride Basic information

Product Name:
Ethyl L-thiazolidine-4-carboxylate hydrochloride
Synonyms:
  • (R)-4-Thiazolidinecarboxylic acid ethyl ester hydrochloride
  • ETHYL L-THIAZOLIDINE-4-CARBOXYLATE HYDROCHLORIDE
  • 4-thiazolidinecarboxylic acid ethyl ester hydrochloride
  • ETHYL L-THIAZOLIDINE-4-CARBOXYLATE HCL
  • Thiazolidine-4-carboxylate hydrochloride
  • ethylthiazolidine-4-carboxylatehydrochloride
  • Ethyl (4R)-thiazolidine-4-carboxylate hydrochloride
  • Pidotimod Impurity 3 HCl
CAS:
86028-91-3
MF:
C6H12ClNO2S
MW:
197.68
EINECS:
1806241-263-5
Mol File:
86028-91-3.mol
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Ethyl L-thiazolidine-4-carboxylate hydrochloride Chemical Properties

storage temp. 
Inert atmosphere,Room Temperature
Appearance
White to off-white Solid
optical activity
Consistent with structure
InChI
InChI=1/C6H11NO2S.ClH/c1-2-9-6(8)5-3-10-4-7-5;/h5,7H,2-4H2,1H3;1H/t5-;/s3
InChIKey
SQRLNYSSTHJCIU-USHJBNIQNA-N
SMILES
[C@H]1(CSCN1)C(OCC)=O.Cl |&1:0,r|
CAS DataBase Reference
86028-91-3(CAS DataBase Reference)
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Safety Information

HS Code 
2934999090
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Ethyl L-thiazolidine-4-carboxylate hydrochloride Usage And Synthesis

Description

Ethyl L-thiazolidine-4-carboxylate hydrochloride (formula, C6H11NO2S·HCl, abbreviation ET4CH),  is one of the analogues of L-proline, which can act as an important intermediate for the synthesis of pidotimod.[1]

References

[1] Qiu, J., Wang*, P., Hu, S., He, H., Huang, H., Zhao, Y., Han, J., Liu, H., & Guo, Y. (2021). 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. Journal of Chemical & Engineering Data, 66 4, 1821–1830. https://doi.org/10.1021/acs.jced.1c00079

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