Now Is The Time For You To Know The Truth About 52287-51-1

As far as I know, this compound(52287-51-1)Recommanded Product: 6-Bromo-2,3-dihydrobenzo[b][1,4]dioxine can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Recommanded Product: 6-Bromo-2,3-dihydrobenzo[b][1,4]dioxine. Aromatic heterocyclic compounds can also be classified according to the number of heteroatoms contained in the heterocycle: single heteroatom, two heteroatoms, three heteroatoms and four heteroatoms. Compound: 6-Bromo-2,3-dihydrobenzo[b][1,4]dioxine, is researched, Molecular C8H7BrO2, CAS is 52287-51-1, about Ceramic boron carbonitrides for unlocking organic halides with visible light. Author is Yuan, Tao; Zheng, Meifang; Antonietti, Markus; Wang, Xinchen.

Here, boron carbonitride (BCN) ceramics were such a system and can reduce organic halides, including (het)aryl and alkyl halides, with visible light irradn was reported. Cross-coupling of halides to afford new C-H, C-C, and C-S bonds was proceeded at ambient reaction conditions. Hydrogen, (het)aryl, and sulfonyl groups were introduced into the arenes and heteroarenes at the designed positions by means of mesolytic C-X (carbon-halogen) bond cleavage in the absence of any metal-based catalysts or ligands. BCN was used not only for half reactions, like reduction reactions with a sacrificial agent, but also redox reactions through oxidative and reductive interfacial electron transfer. The BCN photocatalyst showed tolerance to different substituents and conserved activity after five recycles. The apparent metal-free system opened new opportunities for a wide range of organic catalysts using light energy and sustainable materials, which were metal-free, inexpensive and stable.

As far as I know, this compound(52287-51-1)Recommanded Product: 6-Bromo-2,3-dihydrobenzo[b][1,4]dioxine can be applied in many ways, which is helpful for the development of experiments. Therefore many people are doing relevant researches.

Reference:
Pyrazole – Wikipedia,
Pyrazoles – an overview | ScienceDirect Topics