2-(2-Iodoethyl)-1, 3-dioxolane

95%

Reagent Code: #200771
fingerprint
CAS Number 83665-55-8

science Other reagents with same CAS 83665-55-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 228.03 g/mol
Formula C₅H₉IO₂
badge Registry Numbers
MDL Number MFCD25964997
inventory_2 Storage & Handling
Storage -20°C, Sealed, Dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its iodoalkyl group enables alkylation reactions, making it valuable for introducing functionalized side chains. The dioxolane ring acts as a protected form of a carbonyl compound, allowing controlled deprotection to reveal aldehydes or ketones during multistep syntheses. Commonly employed in the development of central nervous system agents and antitumor compounds due to its ability to cross cell membranes and participate in targeted molecular constructions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿990.00
inventory 1g
10-20 days ฿2,580.00
inventory 5g
10-20 days ฿11,040.00
2-(2-Iodoethyl)-1, 3-dioxolane
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its iodoalkyl group enables alkylation reactions, making it valuable for introducing functionalized side chains. The dioxolane ring acts as a protected form of a carbonyl compound, allowing controlled deprotection to reveal aldehydes or ketones during multistep syntheses. Commonly employed in the development of central nervous system agents and antitumor compounds due to its ability t

Used as an intermediate in organic synthesis, particularly in the preparation of bioactive molecules and pharmaceuticals. Its iodoalkyl group enables alkylation reactions, making it valuable for introducing functionalized side chains. The dioxolane ring acts as a protected form of a carbonyl compound, allowing controlled deprotection to reveal aldehydes or ketones during multistep syntheses. Commonly employed in the development of central nervous system agents and antitumor compounds due to its ability to cross cell membranes and participate in targeted molecular constructions.

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...