Ethyl 3-bromo-2-oxopentanoate

98%

Reagent Code: #182340
fingerprint
CAS Number 113264-43-0

science Other reagents with same CAS 113264-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.06 g/mol
Formula C₇H₁₁BrO₃
thermostat Physical Properties
Boiling Point 232.307°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its α-bromo ketoester structure makes it valuable for introducing functionalized side chains in heterocyclic compounds. Commonly employed in condensation reactions to build complex molecules, including active pharmaceutical ingredients (APIs). Also utilized in the synthesis of α-substituted carbonyl compounds through nucleophilic substitution or metal-catalyzed coupling reactions. Its reactivity allows for easy modification in multi-step synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿2,440.00
inventory 100mg
10-20 days ฿5,920.00
inventory 1g
10-20 days ฿22,150.00
inventory 5g
10-20 days ฿83,990.00
inventory 250mg
10-20 days ฿8,870.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 3-bromo-2-oxopentanoate
No image available

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its α-bromo ketoester structure makes it valuable for introducing functionalized side chains in heterocyclic compounds. Commonly employed in condensation reactions to build complex molecules, including active pharmaceutical ingredients (APIs). Also utilized in the synthesis of α-substituted carbonyl compounds through nucleophilic substitution or metal-catalyzed coupling reactions. Its react

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its α-bromo ketoester structure makes it valuable for introducing functionalized side chains in heterocyclic compounds. Commonly employed in condensation reactions to build complex molecules, including active pharmaceutical ingredients (APIs). Also utilized in the synthesis of α-substituted carbonyl compounds through nucleophilic substitution or metal-catalyzed coupling reactions. Its reactivity allows for easy modification in multi-step 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...