4-Thiazolidinecarboxylic acid, (4R)-


Chemical Name: 4-Thiazolidinecarboxylic acid, (4R)-
CAS Number: 34592-47-7
Product Number: AG00352T(AGN-PC-0O95LU)
Synonyms:
MDL No:
Molecular Formula: C4H7NO2S
Molecular Weight: 133.1689

Identification/Properties


Properties
MP:
190-200 °C (dec.);(lit.);
BP:
350.3°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Refractive Index:
-200 ° (C=1, 1mol/L NaOH)
Computed Properties
Molecular Weight:
133.165g/mol
XLogP3:
-2.3
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
133.02g/mol
Monoisotopic Mass:
133.02g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
106
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
1
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
2811
Hazard Statements:
H301-H312+H332-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P310+P330-P302+P352+P312-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P403+P233-P405-P501
Class:
6.1
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



L-4-Thiazolidinecarboxylic acid, also known as thiazolidine-4-carboxylic acid, is a versatile compound commonly employed in chemical synthesis. Its unique structure containing a thiazolidine ring and a carboxylic acid functional group lends itself well to various synthetic reactions, making it a valuable building block in organic chemistry.In chemical synthesis, L-4-Thiazolidinecarboxylic acid can be utilized as a starting material for the preparation of diverse compounds with pharmaceutical, agrochemical, and material science applications. Its reactivity allows for the introduction of different functional groups through processes such as acylation, alkylation, and condensation reactions, enabling the creation of complex molecules.Moreover, the thiazolidine ring present in L-4-Thiazolidinecarboxylic acid offers an opportunity for further modification, providing access to a range of structurally diverse products. This versatility makes it a key component in the development of novel compounds with potential biological activities or therapeutic properties.Overall, the application of L-4-Thiazolidinecarboxylic acid in chemical synthesis showcases its importance as a valuable intermediate in the creation of functional molecules with various industrial and research applications.