2-((9-Iodonon-2-Yn-1-Yl)Oxy)Tetrahydro-2H-Pyran

95%

Reagent Code: #200607
fingerprint
CAS Number 106853-43-4

science Other reagents with same CAS 106853-43-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.24 g/mol
Formula C₁₄H₂₃IO₂
badge Registry Numbers
MDL Number MFCD29917062
inventory_2 Storage & Handling
Storage Room temperature

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, especially in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, making it valuable in bioconjugation and drug discovery research. The iodo group enables further functionalization through cross-coupling reactions such as Sonogashira or Stille couplings. Additionally, the tetrahydropyran moiety provides structural stability and is commonly found in bioactive molecules, enhancing its utility in medicinal chemistry for building oxygen-containing heterocycles.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,990.00
inventory 250mg
10-20 days ฿23,960.00
inventory 1g
10-20 days ฿47,930.00
2-((9-Iodonon-2-Yn-1-Yl)Oxy)Tetrahydro-2H-Pyran
No image available

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, especially in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, making it valuable in bioconjugation and drug discovery research. The iodo group enables further functionalization through cross-coupling reactions such as Sonogashira or Stille couplings. Additionally, the tetrahydropyran moiety provid

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, especially in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, making it valuable in bioconjugation and drug discovery research. The iodo group enables further functionalization through cross-coupling reactions such as Sonogashira or Stille couplings. Additionally, the tetrahydropyran moiety provides structural stability and is commonly found in bioactive molecules, enhancing its utility in medicinal chemistry for building oxygen-containing heterocycles.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...