1-(Benzyloxy)-2-bromo-4-fluorobenzene

98%

Reagent Code: #153463
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CAS Number 660842-05-7

science Other reagents with same CAS 660842-05-7

blur_circular Chemical Specifications

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Weight 281.13 g/mol
Formula C₁₃H₁₀BrFO
badge Registry Numbers
MDL Number MFCD09839108
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its structure, featuring a bromine substituent suitable for cross-coupling reactions and a fluorine for introducing fluorinated motifs, allows for selective functionalization in multi-step reactions, making it valuable in creating bioactive molecules. The benzyloxy group serves as a protecting group for the phenolic hydroxy functionality, which can be deprotected under controlled conditions later in the synthesis. Commonly employed in palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds, it helps build complex aromatic systems found in drug candidates. Also utilized in the preparation of benzoxazole derivatives and other heterocyclic compounds with potential medicinal properties.

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inventory 1g
10-20 days ฿1,680.00

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1-(Benzyloxy)-2-bromo-4-fluorobenzene
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its structure, featuring a bromine substituent suitable for cross-coupling reactions and a fluorine for introducing fluorinated motifs, allows for selective functionalization in multi-step reactions, making it valuable in creating bioactive molecules. The benzyloxy group serves as a protecting group for the phenolic hydroxy functionality, which can be deprotecte

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds. Its structure, featuring a bromine substituent suitable for cross-coupling reactions and a fluorine for introducing fluorinated motifs, allows for selective functionalization in multi-step reactions, making it valuable in creating bioactive molecules. The benzyloxy group serves as a protecting group for the phenolic hydroxy functionality, which can be deprotected under controlled conditions later in the synthesis. Commonly employed in palladium-catalyzed cross-coupling reactions to form carbon-carbon bonds, it helps build complex aromatic systems found in drug candidates. Also utilized in the preparation of benzoxazole derivatives and other heterocyclic compounds with potential medicinal properties.

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