Ethyl 3-fluoro-4-formylbenzoate

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Reagent Code: #183700
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CAS Number 1640117-38-9

science Other reagents with same CAS 1640117-38-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.18 g/mol
Formula C₁₀H₉FO₃
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MDL Number MFCD28795855
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its aldehyde and ester functional groups allow for versatile chemical modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions and condensation processes to introduce fluorinated aromatic moieties into drug candidates. Also utilized in the development of agrochemicals and specialty polymers where fluorine substitution enhances stability and reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,370.00
inventory 250mg
10-20 days ฿2,460.00
inventory 1g
10-20 days ฿6,620.00
inventory 5g
10-20 days ฿23,170.00

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Ethyl 3-fluoro-4-formylbenzoate
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its aldehyde and ester functional groups allow for versatile chemical modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions and condensation processes to introduce fluorinated aromatic moieties into drug candidates. Also utilized in the development of agro

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the production of non-steroidal anti-inflammatory drugs (NSAIDs) and other bioactive molecules. Its aldehyde and ester functional groups allow for versatile chemical modifications, enabling the construction of complex aromatic structures. Commonly employed in cross-coupling reactions and condensation processes to introduce fluorinated aromatic moieties into drug candidates. Also utilized in the development of agrochemicals and specialty polymers where fluorine substitution enhances stability and reactivity.

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