Can You Really Do Chemisty Experiments About C8H9NO2

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The dynamic chemical diversity of the numerous elements, ions and molecules that constitute the basis of life provides wide challenges and opportunities for research,SDS of cas: 22013-33-8, In a article, mentioned the application of 22013-33-8, molecular formula is C8H9NO2

Novel benzothiazole derivatives have been synthesised via the corresponding imino-1,2,3-dithiazoles. The cytotoxicity of some of these polyheterocyclic compounds was studied. Our results show that 2-cyano derivatives exhibit a medium in vitro antitumour activity.

Balanced chemical reaction does not necessarily reveal either the individual elementary reactions by which a reaction occurs or its rate law.SDS of cas: 22013-33-8. This is the end of this tutorial post, and I hope it has helped your research about 22013-33-8

Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

What Kind of Chemistry Facts Are We Going to Learn About C8H9NO2

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In light of the importance of N-fused heterocycles in pharmaceuticals, there is continuing interest in research on N-fused heterocycles and their preparation. A new and efficient reductive dearomatization-initiated intramolecular cyclization reaction with a broad scope has been developed, affording 3,4,6,7-tetrahydro-2H-pyrimido[1,6-c]quinazolin-2-imine derivatives. Notably, this type of compound showed good inhibitory activity against specific kinases and human cancer cell lines. These results might mean a new molecular scaffold for the development of new antitumor agents.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Downstream Synthetic Route Of C8H9NO2

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The invention relates to triazines and the use thereof to inhibit lysophosphatidic acid acyltransferase beta (LPAAT-beta) activity. The invention further relates to methods of treating cancer using said triazines. The invention also relates to methods for screening for LPAAT-beta activity

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Extended knowledge of 2,3-Dihydrobenzo[b][1,4]dioxin-6-amine

You can get involved in discussing the latest developments in this exciting area about 22013-33-8. Formula: C8H9NO2

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A gold-catalyzed post-Ugi cascade transformation for the synthesis of 2-pyridones is described. The process involves furan?alkyne cyclization followed by furan ring-opening and cleavage of the isocyanide-originated fragment. The initially formed cis double bond can isomerize into a more stable trans double bond upon prolonged exposure to a strong Br°nsted acid. Thus, the overall strategy provides a viable access towards two types of 2-pyridones.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem

Downstream Synthetic Route Of C10H10O3

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A copper-catalyzed asymmetric oxidative cross-coupling reaction of 2-naphthols with aryl methyl ketones has been developed. This transformation provides an efficient route to various functionalized naphtho[2,1-b]furan-1(2H)-ones in an enantiomerically enriched manner with molecular oxygen in air as the oxidant (52-89% yields, up to 87% ee). The reaction leads to the formation of a new quaternary carbon center within 3(2H)-furanones.

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Reference:
Benzodioxan,
1,4-Benzodioxane | C8H8O2 – PubChem