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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-Thiazolidinone, 5-[[4-(diethylamino)phenyl]methylene]-2-thioxo-

CCN(c1ccc(cc1)/C=C/1SC(=S)NC1=O)CC Request for Quotation
Chemical Name: 4-Thiazolidinone, 5-[[4-(diethylamino)phenyl]methylene]-2-thioxo-
CAS Number: 35778-58-6
Product Number: AG003M5S(AGN-PC-0K2EIH)
Synonyms:
MDL No:
Molecular Formula: C14H16N2OS2
Molecular Weight: 292.4196

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Computed Properties
Molecular Weight:
292.415g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
4
Exact Mass:
292.07g/mol
Monoisotopic Mass:
292.07g/mol
Topological Polar Surface Area:
89.7A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
383
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
1
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


5-(4-(Diethylamino)benzylidene)-2-thioxothiazolidin-4-one, commonly known as $name$, is a versatile compound that finds extensive utility in chemical synthesis. One of its key applications is as a catalyst in organic reactions, where it serves as a powerful tool for promoting various transformations with high efficiency and selectivity. This compound has been particularly valued for its ability to mediate the formation of carbon-carbon and carbon-heteroatom bonds, essential steps in the synthesis of complex organic molecules. In addition, $name$ has shown promise in asymmetric synthesis, enabling the production of chiral compounds with high enantiomeric purity. Its unique structure, combining a thiazolidinone ring with a diethylamino-substituted benzylidene moiety, imparts specific reactivity that can be harnessed in a wide range of chemical transformations. Whether used in traditional organic synthesis or cutting-edge catalysis, $name$ continues to demonstrate its significance as a valuable tool for synthetic chemists striving to access new molecules and expand the frontiers of chemical knowledge.