Ethyl 3-fluoro-4-methoxybenzoylformate

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Reagent Code: #185083
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CAS Number 345-72-2

science Other reagents with same CAS 345-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.21 g/mol
Formula C₁₁H₁₁FO₄
badge Registry Numbers
MDL Number MFCD06201699
inventory_2 Storage & Handling
Storage -20°C, argon-filled

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its structure allows for selective derivatization, making it valuable in building complex molecules with enhanced metabolic stability and bioavailability. Commonly employed in the preparation of active ingredients in crop protection agents and in the development of fluorinated analogs of bioactive compounds. The ester and keto functionalities enable coupling reactions and cyclizations, facilitating its use in heterocycle formation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿840.00
inventory 1g
10-20 days ฿4,010.00
inventory 250mg
10-20 days ฿1,020.00

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Ethyl 3-fluoro-4-methoxybenzoylformate
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its structure allows for selective derivatization, making it valuable in building complex molecules with enhanced metabolic stability and bioavailability. Commonly employed in the preparation of active ingredients in crop protection agents and in the development of fluorinated analogs of bioactive compounds. The ester and keto functionalities enable coupling reactions and cyclizations, facilitating its use in he

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its structure allows for selective derivatization, making it valuable in building complex molecules with enhanced metabolic stability and bioavailability. Commonly employed in the preparation of active ingredients in crop protection agents and in the development of fluorinated analogs of bioactive compounds. The ester and keto functionalities enable coupling reactions and cyclizations, facilitating its use in heterocycle formation.

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