Ethyl 3-iodopropanoate

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Reagent Code: #182315
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CAS Number 6414-69-3

science Other reagents with same CAS 6414-69-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.03 g/mol
Formula C₅H₉IO₂
thermostat Physical Properties
Boiling Point 203°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactivity allows for the introduction of ester and alkyl iodide functionalities, making it valuable in carbon chain extension reactions. Commonly employed in the synthesis of heterocyclic compounds and active pharmaceutical ingredients (APIs) where a three-carbon spacer with reactive handles is needed. Also utilized in the preparation of propanoic acid derivatives through hydrolysis or reduction. Its iodine moiety facilitates coupling reactions, including palladium-catalyzed cross-couplings, useful in medicinal chemistry and agrochemical research.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿480.00
inventory 25g
10-20 days ฿8,150.00
inventory 5g
10-20 days ฿1,670.00
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Ethyl 3-iodopropanoate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactivity allows for the introduction of ester and alkyl iodide functionalities, making it valuable in carbon chain extension reactions. Commonly employed in the synthesis of heterocyclic compounds and active pharmaceutical ingredients (APIs) where a three-carbon spacer with reactive handles is needed. Also utilized in the preparation of propanoic acid derivatives through hydrolysis o

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. Its reactivity allows for the introduction of ester and alkyl iodide functionalities, making it valuable in carbon chain extension reactions. Commonly employed in the synthesis of heterocyclic compounds and active pharmaceutical ingredients (APIs) where a three-carbon spacer with reactive handles is needed. Also utilized in the preparation of propanoic acid derivatives through hydrolysis or reduction. Its iodine moiety facilitates coupling reactions, including palladium-catalyzed cross-couplings, useful in medicinal chemistry and agrochemical research.

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