Triethyl 4-phosphonocrotonate

cis and trans,94%

Reagent Code: #240555
fingerprint
CAS Number 10236-14-3

science Other reagents with same CAS 10236-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.23 g/mol
Formula C₁₀H₁₉O₅P
badge Registry Numbers
MDL Number MFCD00009192
thermostat Physical Properties
Boiling Point 135°C 0.4mm Hg (Lit.)
inventory_2 Storage & Handling
Density 1.1280
Storage Room temperature, seal, dry

description Product Description

Used as a key reagent in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) olefination reactions to form α,β-unsaturated esters and other conjugated systems. Its phosphonate group stabilizes carbanions, enabling efficient carbon-carbon bond formation under mild conditions. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and natural products where precise alkene geometry is required. The ethyl ester groups enhance solubility in organic solvents, facilitating reaction handling and purification. Also employed in the preparation of bioactive molecules and functional materials due to its versatility and reliability in constructing olefinic frameworks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,550.00
inventory 5g
10-20 days ฿10,140.00
Triethyl 4-phosphonocrotonate
No image available

Used as a key reagent in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) olefination reactions to form α,β-unsaturated esters and other conjugated systems. Its phosphonate group stabilizes carbanions, enabling efficient carbon-carbon bond formation under mild conditions. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and natural products where precise alkene geometry is required. The ethyl ester groups enhance solubility in organic solvents, facilitating reaction ha

Used as a key reagent in organic synthesis, particularly in Horner-Wadsworth-Emmons (HWE) olefination reactions to form α,β-unsaturated esters and other conjugated systems. Its phosphonate group stabilizes carbanions, enabling efficient carbon-carbon bond formation under mild conditions. Commonly applied in the synthesis of pharmaceuticals, agrochemicals, and natural products where precise alkene geometry is required. The ethyl ester groups enhance solubility in organic solvents, facilitating reaction handling and purification. Also employed in the preparation of bioactive molecules and functional materials due to its versatility and reliability in constructing olefinic frameworks.

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...