2-((6-Iodohex-2-Yn-1-Yl)Oxy)Tetrahydro-2H-Pyran
95%
- Product Code: 200578
CAS:
532414-06-5
| Molecular Weight: | 308.16 g./mol | Molecular Formula: | C₁₁H₁₇O₂I |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD29917061 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Room temperature, sealed, dry |
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.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | €397.69 |
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| 250mg | 10-20 days | €695.95 |
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2-((6-Iodohex-2-Yn-1-Yl)Oxy)Tetrahydro-2H-Pyran
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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