Ethyl 3-(5-Methylfuran-2-Yl)-3-Oxopropanoate

Reagent Code: #185523
fingerprint
CAS Number 5896-37-7

science Other reagents with same CAS 5896-37-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.2 g/mol
Formula C₁₀H₁₂O₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. Commonly employed in condensation reactions to form heterocyclic compounds, which are prevalent in bioactive molecules. Also utilized in the development of flavor and fragrance compounds due to its furan moiety, which contributes to aromatic characteristics. Its ketoester functionality enables it to participate in Claisen and Michael addition reactions, broadening its utility in synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,700.00
Ethyl 3-(5-Methylfuran-2-Yl)-3-Oxopropanoate
No image available

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. Commonly employed in condensation reactions to form heterocyclic compounds, which are prevalent in bioactive molecules. Also utilized in the development of flavor and fragrance compounds due to its furan moiety, which contributes to aromatic characteristics. Its ketoester f

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. Commonly employed in condensation reactions to form heterocyclic compounds, which are prevalent in bioactive molecules. Also utilized in the development of flavor and fragrance compounds due to its furan moiety, which contributes to aromatic characteristics. Its ketoester functionality enables it to participate in Claisen and Michael addition reactions, broadening its utility in synthetic pathways.

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...