2-((6-Iodohex-2-Yn-1-Yl)Oxy)Tetrahydro-2H-Pyran

95%

Reagent Code: #200578
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CAS Number 532414-06-5

science Other reagents with same CAS 532414-06-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.16 g/mol
Formula C₁₁H₁₇O₂I
badge Registry Numbers
MDL Number MFCD29917061
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its alkyne functionality allows for click chemistry applications, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in bioorthogonal labeling and drug discovery. The iodine atom serves as a reactive handle for cross-coupling reactions, including Sonogashira and Suzuki couplings, facilitating the construction of larger molecular architectures. The tetrahydropyran ring provides structural stability and can mimic sugar moieties, making it useful in the synthesis of glycosidic analogs and bioactive molecules with enhanced metabolic resistance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,120.00
inventory 250mg
10-20 days ฿26,460.00
2-((6-Iodohex-2-Yn-1-Yl)Oxy)Tetrahydro-2H-Pyran
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Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its alkyne functionality allows for click chemistry applications, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in bioorthogonal labeling and drug discovery. The iodine atom serves as a reactive handle for cross-coupling reactions, including Sonogashira and Suzuki couplings, facilitating the construction of larger molecular archite

Used as a key intermediate in organic synthesis, particularly in the preparation of complex natural products and pharmaceuticals. Its alkyne functionality allows for click chemistry applications, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), enabling efficient conjugation in bioorthogonal labeling and drug discovery. The iodine atom serves as a reactive handle for cross-coupling reactions, including Sonogashira and Suzuki couplings, facilitating the construction of larger molecular architectures. The tetrahydropyran ring provides structural stability and can mimic sugar moieties, making it useful in the synthesis of glycosidic analogs and bioactive molecules with enhanced metabolic resistance.

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