3-((2S,5S)-5-((3R,5R)-3-Hydroxy-6-iodo-5-methylhept-6-en-1-yl)-4-methylenetetrahydrofuran-2-yl)propylpivalate

97%

Reagent Code: #237819
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CAS Number 157322-47-9

science Other reagents with same CAS 157322-47-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 478.4 g/mol
Formula C₂₁H₃₅IO₄
inventory_2 Storage & Handling
Storage -20°C

description Product Description

Used in the synthesis of complex natural products and bioactive molecules, particularly in pharmaceutical research targeting enzyme inhibitors or receptor modulators. Its structural complexity, including stereochemistry and functional groups like the iodinated alkene and pivalate ester, makes it a valuable intermediate in asymmetric synthesis and fragment coupling reactions. Commonly employed in late-stage functionalization due to the reactivity of the iodine moiety, enabling cross-coupling reactions such as Suzuki or Heck reactions. The tetrahydrofuran core with defined stereocenters also supports its use in constructing chiral building blocks for drug development.

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inventory 100mg
10-20 days ฿37,130.00

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3-((2S,5S)-5-((3R,5R)-3-Hydroxy-6-iodo-5-methylhept-6-en-1-yl)-4-methylenetetrahydrofuran-2-yl)propylpivalate
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Used in the synthesis of complex natural products and bioactive molecules, particularly in pharmaceutical research targeting enzyme inhibitors or receptor modulators. Its structural complexity, including stereochemistry and functional groups like the iodinated alkene and pivalate ester, makes it a valuable intermediate in asymmetric synthesis and fragment coupling reactions. Commonly employed in late-stage functionalization due to the reactivity of the iodine moiety, enabling cross-coupling reactions suc

Used in the synthesis of complex natural products and bioactive molecules, particularly in pharmaceutical research targeting enzyme inhibitors or receptor modulators. Its structural complexity, including stereochemistry and functional groups like the iodinated alkene and pivalate ester, makes it a valuable intermediate in asymmetric synthesis and fragment coupling reactions. Commonly employed in late-stage functionalization due to the reactivity of the iodine moiety, enabling cross-coupling reactions such as Suzuki or Heck reactions. The tetrahydrofuran core with defined stereocenters also supports its use in constructing chiral building blocks for drug development.

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