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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)-

2-Thiazolidinethione, 3-acetyl-4-(1-methylethyl)-, (4R)-

CC([C@@H]1CSC(=S)N1C(=O)C)C Request for Quotation
Chemical Name: 2-Thiazolidinethione, 3-acetyl-4-(1-methylethyl)-, (4R)-
CAS Number: 121929-87-1
Product Number: AG0016F6(AGN-PC-0O0CKY)
Synonyms:
MDL No:
Molecular Formula: C8H13NOS2
Molecular Weight: 203.3249

Identification/Properties

Computed Properties
Molecular Weight:
203.318g/mol
XLogP3:
2.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
203.044g/mol
Monoisotopic Mass:
203.044g/mol
Topological Polar Surface Area:
77.7A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
215
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:
H302-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


The (R)-1-(4-isopropyl-2-thioxothiazolidin-3-yl)ethanone compound is a valuable and versatile substance commonly used in chemical synthesis. Its application in organic chemistry lies in its ability to serve as a key building block for the creation of various complex molecules and pharmaceuticals. Through strategic manipulation of its functional groups and reactivity, this compound can participate in a range of reactions such as nucleophilic additions, condensations, and asymmetric synthesis. Chemists often rely on the unique properties of (R)-1-(4-isopropyl-2-thioxothiazolidin-3-yl)ethanone to introduce specific structural motifs or stereochemical elements into target molecules, facilitating the efficient and precise production of desired compounds. By incorporating this compound into synthetic pathways, researchers can access new avenues for chemical innovation and the development of novel materials with enhanced properties.