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Usage

Uses

Used in Organic Synthesis:
(3-phenoxypropyl)boronic acid is used as a reagent or catalyst in organic synthesis reactions, such as Suzuki-Miyaura cross-coupling reactions, for the formation of carbon-carbon bonds. Its reactivity and selectivity make it a valuable tool in the construction of complex organic molecules.
Used in Medicinal Chemistry:
(3-phenoxypropyl)boronic acid is used as a building block in the development of pharmaceuticals due to its ability to form strong and selective interactions with biological targets.
Used in Material Science:
(3-phenoxypropyl)boronic acid is used in the development of new materials due to its ability to form strong and selective interactions with specific functional groups in materials.

Upstream product

• 177950-03-7 2-(3-phenoxypropyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane 
• 588-63-6 3-phenoxypropyl bromide 
• 1746-13-0 allyl phenyl ether 

Downstream Products

• 1440956-09-1 (4,4,4-trifluoro-butoxy)-benzene 
• 622-85-5 propoxybenzene 
• 1746-13-0 allyl phenyl ether 
• 64806-63-9 3-phenoxypropylbenzene 

Relevant academic research and scientific papers

Coupling of Trifluoroacetaldehyde N-Triftosylhydrazone with Organoboronic Acids for the Synthesis of gem-Difluoroalkenes

The synthesis of alkyl gem-difluoroalkenes remains a difficult task in organic synthesis. Here, we report a general and efficient approach for tackling this problem by gem-difluoroolefination of trifluoroacetaldehyde N-triftosylhydrazone with organoboronic acids. This protocol is operationally simple, free of transition metals, and suitable for a broad range of organoboronic acids. Moreover, the utility of the products was demonstrated by further conversion of the gem-difluorovinyl group.

Copper-catalyzed trifluoromethylthiolation of primary and secondary alkylboronic acids

A Cu-catalyzed trifluoromethylthiolation of primary and secondary alkylboronic acids with an electrophilic trifluoromethylthiolating reagent is described. Tolerance for a variety of functional groups was observed.

Copper-promoted trifluoromethylation of primary and secondary alkylboronic acids

New couple: The Cu-promoted trifluoromethylation of primary and secondary alkylboronic acids with TMSCF3 extends the scope of transition-metal-catalyzed trifluoromethylation reactions to sp 3-hybridized carbon centers. It also repres