Ethyl 2-(3-iodopyridin-2-yl)acetate

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Reagent Code: #45572
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CAS Number 1245645-70-8

science Other reagents with same CAS 1245645-70-8

blur_circular Chemical Specifications

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Weight 291.08567 g/mol
Formula C₉H₁₀INO₂
inventory_2 Storage & Handling
Storage 2-8℃, dry, airtight

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs). Its structure is valuable for constructing complex molecules, often utilized in the synthesis of heterocyclic compounds. Additionally, it finds application in research settings for studying enzyme inhibition and receptor binding activities, aiding in the discovery of new therapeutic agents. Its iodine moiety makes it useful in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in medicinal chemistry for building diverse molecular architectures.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,214.00
inventory 50mg
10-20 days ฿11,214.00
inventory 10mg
10-20 days ฿3,492.00

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Ethyl 2-(3-iodopyridin-2-yl)acetate
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Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs). Its structure is valuable for constructing complex molecules, often utilized in the synthesis of heterocyclic compounds. Additionally, it finds application in research settings for studying enzyme inhibition and receptor binding activities, aiding in the discovery of new therapeutic agents. Its iodine moiety makes

Used primarily in organic synthesis, this compound serves as a key intermediate in the development of pharmaceuticals, particularly in the creation of active pharmaceutical ingredients (APIs). Its structure is valuable for constructing complex molecules, often utilized in the synthesis of heterocyclic compounds. Additionally, it finds application in research settings for studying enzyme inhibition and receptor binding activities, aiding in the discovery of new therapeutic agents. Its iodine moiety makes it useful in cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in medicinal chemistry for building diverse molecular architectures.

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