Category: 151509-01-2

Heterocyclic compounds can be divided into two categories: alicyclic heterocycles and aromatic heterocycles. Compounds whose heterocycles in the molecular skeleton cannot reflect aromaticity are called alicyclic heterocyclic compounds. Compound: 151509-01-2, is researched, Molecular C8H11ClN2O2, about Acetic formic anhydride, the main research direction is review acetic formic anhydride formylation alc phenol amine.Formula: C8H11ClN2O2.

A review. Preparation, properties and applications of acetic formic anhydride as a formylating agent for hydroxyl, phenol and amine groups as well as other heteroatoms has been reviewed. Acetic formic anhydride is useful for the synthesis of aldehydes from aromatic Grignard reagents and for preparation of formyl fluoride and diazoacetaldehyde.

As far as I know, this compound(151509-01-2)Formula: C8H11ClN2O2 can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem

Most of the natural products isolated at present are heterocyclic compounds, so heterocyclic compounds occupy an important position in the research of organic chemistry. A compound: 151509-01-2, is researched, SMILESS is O=C(OC)C1=C(CN)N=CC=C1.[H]Cl, Molecular C8H11ClN2O2Journal, Journal of Heterocyclic Chemistry called Synthesis of a new 1,4-dihydropyridine containing the imidazo[1,5-a]pyridine nucleus, Author is Fos, Empar; Bosca, Francisco; Mauleon, David; Carganico, Germano, the main research direction is imidazopyridinyl dihydropyridine preparation calcium channel blocker; antithrombotic imidazopyridinyl dihydropyridine preparation; pyridine imidazopyridinyl preparation; nifedipine imidazopyridinyl analog preparation.Electric Literature of C8H11ClN2O2.

The preparation of the new dihydropyridine di-Et 1,4-dihydro-4-(imidazo[1,5-a]pyridin-8-yl)-2,6-dimethylpyridine-3,5-dicarboxylate (I) is described. After many attempts to prepare the key intermediate aldehyde II by different approaches, this compound was obtained in good yields from Me 2-cyano-3-pyridinecarboxylate. A 3-step procedure involving reduction to the amine, formylation with concomitant cyclization and reduction of the ester group was used. I had activity as calcium antagonist but it was devoid of activity as thromboxane inhibitor.

When you point to this article, it is believed that you are also very interested in this compound(151509-01-2)Electric Literature of C8H11ClN2O2 and due to space limitations, I can only present the most important information.

Reference:
Oxazolidine – Wikipedia,
Oxazolidine | C3H7NO – PubChem