Awesome and Easy Science Experiments about 10097-02-6

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 10097-02-6. HPLC of Formula: C6H12O4.

Chemistry is the experimental science by definition. We want to make observations to prove hypothesis. For this purpose, we perform experiments in the lab. , HPLC of Formula: C6H12O4, 10097-02-6, Name is 2,2-Bis(hydroxymethyl)butyric acid, molecular formula is C6H12O4, belongs to thiazolidines compound. In a document, author is Hossaini, Mahshid, introduce the new discover.

Synthesis and crystal structures of novel (4-phenylthiazol-2(3H)-ylidene) benzamide and ((benzoylimino)-3-(9,10-dioxo-9,10-dihydroanthracen-1-yl)-4-oxothiazolidin-5-ylidene)acetate derivatives

A new approach to the synthesis of new heterocyclic compounds with benzoylisothiocyanate, amines, and 2-bromoacetophenone (phenacyl bromide) fragments in one molecule has been developed. The synthesis method comprises condensation reaction for the preparation of novel (4-phenylthiazol-2(3H)-ylidene) benzamide derivatives. These new compounds were synthesized via one-pot and multicomponent reaction of 2-furanmethylamine, 5-chloro-2-phenoxyaniline, and 1-naphthylamine with phenacyl bromide and substituted benzoylisothiocyanates. Moreover, new series of anthraquinone-thiazole hybrids have been synthesized. These compounds were prepared from unsymmetrical thiourea containing anthraquinone and dialkyl acetylenedicarboxylate. The nature of the compounds was confirmed by IR, (HNMR)-H-1, (CNMR)-C-13, mass spectrometry, and CHNS elemental analysis. The structural elucidation was accomplished by single-crystal X-ray diffraction methods.

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 10097-02-6. HPLC of Formula: C6H12O4.

Reference:
Thiazolidine – Wikipedia,
,Thiazolidine – ScienceDirect.com