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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

4-Thiazolidinecarboxylic acid, 2-thioxo-, (4R)-

OC(=O)[C@@H]1CSC(=S)N1 Request for Quotation
Chemical Name: 4-Thiazolidinecarboxylic acid, 2-thioxo-, (4R)-
CAS Number: 98169-56-3
Product Number: AG003BWR(AGN-PC-0OOTV8)
Synonyms:
MDL No:
Molecular Formula: C4H5NO2S2
Molecular Weight: 163.2180

Identification/Properties

Properties
MP:
165-170°C
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
163.209g/mol
XLogP3:
0.5
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
1
Exact Mass:
162.976g/mol
Monoisotopic Mass:
162.976g/mol
Topological Polar Surface Area:
107A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
159
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:
Warning
UN#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


(R)-2-Thioxothiazolidine-4-carboxylic acid, a versatile compound widely used in chemical synthesis, serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and advanced materials. In organic synthesis, this compound acts as a key intermediate in the production of diverse functional molecules by participating in a range of reactions, such as cyclization, condensation, and oxidation processes. Its unique structural features make it a preferred choice for introducing sulfur-based functionalities into target molecules, thereby enhancing their biological activities or material properties. Additionally, the presence of a thiazolidine ring in the structure imparts specific stereochemistry, further expanding the utility of (R)-2-Thioxothiazolidine-4-carboxylic acid in the design of chiral compounds with defined spatial arrangements. This compound's role as a synthetic tool in organic chemistry highlights its significance in enabling the rapid and efficient construction of complex chemical compounds for various scientific and industrial applications.