Ethyl 3-(3-fluoropyridin-2-yl)propanoate

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Reagent Code: #184925
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CAS Number 1427360-81-3

science Other reagents with same CAS 1427360-81-3

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Weight 197.21 g/mol
Formula C₁₀H₁₂FNO₂
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MDL Number MFCD23709077
inventory_2 Storage & Handling
Storage Room temperature

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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables effective binding to enzyme active sites, making it valuable in creating compounds with high selectivity and potency. Commonly employed in medicinal chemistry for constructing fluorinated heterocyclic systems, which improve metabolic stability and bioavailability in drug candidates. Also utilized in the preparation of neuroactive compounds due to its ability to cross the blood-brain barrier.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,880.00
inventory 250mg
10-20 days ฿6,430.00
inventory 1g
10-20 days ฿20,750.00

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Ethyl 3-(3-fluoropyridin-2-yl)propanoate
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables effective binding to enzyme active sites, making it valuable in creating compounds with high selectivity and potency. Commonly employed in medicinal chemistry for constructing fluorinated heterocyclic systems, which improve metabolic stability and bioavailability in drug candidates. Also utilized in the preparation of neuroactive c

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure enables effective binding to enzyme active sites, making it valuable in creating compounds with high selectivity and potency. Commonly employed in medicinal chemistry for constructing fluorinated heterocyclic systems, which improve metabolic stability and bioavailability in drug candidates. Also utilized in the preparation of neuroactive compounds due to its ability to cross the blood-brain barrier.

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