5-Fluoro-2-hydroxy-3-methylbenzaldehyde

95%

Reagent Code: #188325
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CAS Number 704884-74-2

science Other reagents with same CAS 704884-74-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 154.1384 g/mol
Formula C₈H₇FO₂
badge Registry Numbers
MDL Number MFCD04039244
thermostat Physical Properties
Melting Point 44 - 49 ℃ - lit.
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its structure supports the construction of complex molecules in medicinal chemistry, especially in the design of kinase inhibitors and anti-inflammatory agents. The aldehyde and hydroxyl functional groups allow for versatile derivatization, enabling use in condensation reactions, heterocycle formation, and as a building block in multi-step organic syntheses. Also employed in the preparation of fluorescent probes and agrochemicals due to the electron-withdrawing effect of the fluorine atom, which influences reactivity and binding characteristics.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿690.00
inventory 1g
10-20 days ฿2,760.00
inventory 5g
10-20 days ฿13,640.00

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5-Fluoro-2-hydroxy-3-methylbenzaldehyde
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of fluorinated organic compounds with enhanced metabolic stability and bioavailability. Its structure supports the construction of complex molecules in medicinal chemistry, especially in the design of kinase inhibitors and anti-inflammatory agents. The aldehyde and hydroxyl functional groups allow for versatile derivatization, enabling use in condensation reactions, heterocycle formation, and as a building block in multi-step organic syntheses. Also employed in the preparation of fluorescent probes and agrochemicals due to the electron-withdrawing effect of the fluorine atom, which influences reactivity and binding characteristics.
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