Application of 3395-91-3

This compound(Methyl 3-bromopropanoate)Safety of Methyl 3-bromopropanoate was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

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: 3395-91-3, is researched, Molecular C4H7BrO2, about Reductive sp3-sp2 Coupling Reactions Enable Late-Stage Modification of Pharmaceuticals, the main research direction is chloroaminopyrimidine bromide alkyl halide chemoselective cross electrophile reductive coupling.Safety of Methyl 3-bromopropanoate.

Late-stage derivatization of pharmaceutically relevant scaffolds relies on the availability of highly functional-group tolerant reactions. Reactions that increase the sp3 character of mols. enable the pursuit of more selective and well-tolerated pharmaceuticals. Herein, we report the use of sp3-sp2 cross-electrophile reductive couplings to modify a generic ATP-competitive kinase inhibitor with a broad range of primary and secondary alkyl halide coupling partners.

This compound(Methyl 3-bromopropanoate)Safety of Methyl 3-bromopropanoate was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Benzothiophene – Wikipedia,
Benzothiophene | C8H6S – PubChem