Chemistry is the science of change. But why do chemical reactions take place? Why do chemicals react with each other? The answer is in thermodynamics and kinetics, Quality Control of 3-(3,5-Di-tert-butyl-1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)propanoic acid, 83237-15-4, Name is 3-(3,5-Di-tert-butyl-1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)propanoic acid, SMILES is O=C(CCC1(C=C(C(C)(C)C)C(=O)C(C(C)(C)C)=C1)O)O, belongs to thiazolidines compound. In a document, author is Ousidi, Abdellah N’ait, introduce the new discover.
New polysubstituted monoterpenic thiazolidinones: synthesis, spectroscopic and crystal structure studies
The synthesis of three new polysubstituted monoterpenic thiazolidin-4-ones, namely (Z)-3-methyl-2-{(E)-[(1R, 4R)-1,7,7-trimethylbicyclo[2.2.1]heptan-2-yl-idene]hydrazinylidene}thiazolidin-4-one, C14H21N3OS (2), (2Z, 5Z)-5-[(dimethylamino)methylidene]-2-{(E)-[(1R, 4R)-1,7,7-trimethylbicyclo[2.2.1]heptan2- ylidene]hydrazinylidene}thiazolidin-4-one, C16H24N4OS (3), and (2Z, 5Z)-5[(dimethylamino)methylidene]-3-methyl-2-{(E)-[(1R, 4R)-1,7,7-trimethylbicyclo[ 2.2.1]heptan-2-ylidene]hydrazinylidene}thiazolidin-4-one, C17H26N4OS (4), is reported, starting from the corresponding thiosemicarbazones obtained from naturally occurring (R)-camphor. All the newly obtained thiazolidin-4-ones have been fully characterized by HRMS and H-1 and C-13 (1D and 2D) NMR spectroscopy. Two of them, i.e. 2 and 3, were identified by single-crystal X- ray crystallography, confirming the synthetic pathway and the spectroscopic analyses. In 3, there are two roughly identical molecules within the asymmetric unit with the same absolute configuration. These two molecules are linked through N-H center dot center dot center dot O hydrogen bonds, building an R-2(2)(8) graph-set motif.
A reaction mechanism is the microscopic path by which reactants are transformed into products. Each step is an elementary reaction. In my other articles, you can also check out more blogs about 83237-15-4. Quality Control of 3-(3,5-Di-tert-butyl-1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)propanoic acid.
Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com