3-Iodo-1-(Tetrahydro-2H-Pyran-2-Yl)-1H-Pyrazole-4-Carbaldehyde

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Reagent Code: #200986
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CAS Number 1627924-19-9

science Other reagents with same CAS 1627924-19-9

blur_circular Chemical Specifications

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Weight 306.1 g/mol
Formula C₉H₁₁IN₂O₂
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Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in the development of kinase inhibitors and other targeted therapies. The aldehyde group enables further derivatization through reactions such as Wittig, reductive amination, or condensation, facilitating the creation of diverse compound libraries for drug discovery. Additionally, the iodine moiety supports cross-coupling reactions like Suzuki or Sonogashira, expanding its utility in building complex heterocyclic systems. Commonly employed in medicinal chemistry for optimizing lead compounds with improved potency and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,530.00
inventory 250mg
10-20 days ฿17,330.00
inventory 1g
10-20 days ฿33,260.00

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3-Iodo-1-(Tetrahydro-2H-Pyran-2-Yl)-1H-Pyrazole-4-Carbaldehyde
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in the development of kinase inhibitors and other targeted therapies. The aldehyde group enables further derivatization through reactions such as Wittig, reductive amination, or condensation, facilitating the creation of diverse compound libraries for drug discovery. Additionally, the iodine moiety supports cross-co

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceutical research. Its structure allows for selective functionalization, making it valuable in the development of kinase inhibitors and other targeted therapies. The aldehyde group enables further derivatization through reactions such as Wittig, reductive amination, or condensation, facilitating the creation of diverse compound libraries for drug discovery. Additionally, the iodine moiety supports cross-coupling reactions like Suzuki or Sonogashira, expanding its utility in building complex heterocyclic systems. Commonly employed in medicinal chemistry for optimizing lead compounds with improved potency and selectivity.

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