Szczepanski, Jacek et al. published their research in Molbank in 2020 | CAS: 92972-48-0

2,4-Dichlorothiazole-5-carbaldehyde (cas: 92972-48-0) belongs to thiazole derivatives. Thiazoles frequently appear in peptide studies. Thiazoles can also be used as protected formyl groups, which can be released in later stages of complex natural product synthesis. Thiazole sulfonation occurs only under forcing conditions: the action of oleum at 250 °C for 3 hours in the presence of mercury(II) sulfate leads to 65% formation of 5-thiazole sulfonic acid.Related Products of 92972-48-0

Synthesis of a new [3-(4-chlorophenyl)-4-oxo-1, 3-thiazolidin-5-ylidene]acetic acid derivative was written by Szczepanski, Jacek;Tuszewska, Helena;Trotsko, Nazar. And the article was included in Molbank in 2020.Related Products of 92972-48-0 This article mentions the following:

The new I was synthesized from II using di-Me acetylenedicarboxylate as thia-Michael reaction acceptor. In the experiment, the researchers used many compounds, for example, 2,4-Dichlorothiazole-5-carbaldehyde (cas: 92972-48-0Related Products of 92972-48-0).

2,4-Dichlorothiazole-5-carbaldehyde (cas: 92972-48-0) belongs to thiazole derivatives. Thiazoles frequently appear in peptide studies. Thiazoles can also be used as protected formyl groups, which can be released in later stages of complex natural product synthesis. Thiazole sulfonation occurs only under forcing conditions: the action of oleum at 250 °C for 3 hours in the presence of mercury(II) sulfate leads to 65% formation of 5-thiazole sulfonic acid.Related Products of 92972-48-0

Referemce:
Thiazole | C3H3NS – PubChem,
Thiazole | chemical compound | Britannica