2-(Bromomethyl)-1-Fluoro-4-Methoxybenzene

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Reagent Code: #151099
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CAS Number 91319-42-5

science Other reagents with same CAS 91319-42-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.05 g/mol
Formula C₈H₈BrFO
badge Registry Numbers
MDL Number MFCD11617285
thermostat Physical Properties
Boiling Point 252.5±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.488±0.06 g/cm3(Predicted)
Storage Room temperature, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the bromomethyl group enables further functionalization through cross-coupling reactions. Its structure supports the introduction of fluorine, which can enhance metabolic stability and bioavailability in active pharmaceutical ingredients. Also employed in the preparation of agrochemicals and specialty organic compounds requiring selective substitution patterns on aromatic rings. The compound’s reactivity makes it valuable in building complex molecules in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,430.00
inventory 250mg
10-20 days ฿5,460.00
inventory 1g
10-20 days ฿11,500.00
inventory 5g
10-20 days ฿34,500.00

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2-(Bromomethyl)-1-Fluoro-4-Methoxybenzene
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the bromomethyl group enables further functionalization through cross-coupling reactions. Its structure supports the introduction of fluorine, which can enhance metabolic stability and bioavailability in active pharmaceutical ingredients. Also employed in the preparation of agrochemicals and specialty organic compounds requiring selective substitution patterns on aromatic ring
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated drug candidates where the bromomethyl group enables further functionalization through cross-coupling reactions. Its structure supports the introduction of fluorine, which can enhance metabolic stability and bioavailability in active pharmaceutical ingredients. Also employed in the preparation of agrochemicals and specialty organic compounds requiring selective substitution patterns on aromatic rings. The compound’s reactivity makes it valuable in building complex molecules in medicinal chemistry research.
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