Ethyl 3-Bromo-2-(bromomethyl)propionate

>97.0%(GC)

Reagent Code: #183023
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CAS Number 58539-11-0

science Other reagents with same CAS 58539-11-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.95 g/mol
Formula C₆H₁₀Br₂O₂
badge Registry Numbers
MDL Number MFCD00034154
thermostat Physical Properties
Boiling Point 86 °C/0.3kPa
inventory_2 Storage & Handling
Density 1.72g/mL
Storage Room temperature, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its dual bromine functionality allows for selective substitution reactions, making it valuable in constructing complex molecules, including cyclopropane derivatives through reactions with nucleophilic carbon compounds like enolates or alkenes via double alkylation processes. Commonly employed in the development of active pharmaceutical ingredients where a propionate backbone with reactive sites is needed. Also utilized in the synthesis of specialty polymers and functionalized esters for fine chemical applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,180.00
inventory 25g
10-20 days ฿14,100.00
inventory 5g
10-20 days ฿2,084.50
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Ethyl 3-Bromo-2-(bromomethyl)propionate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its dual bromine functionality allows for selective substitution reactions, making it valuable in constructing complex molecules, including cyclopropane derivatives through reactions with nucleophilic carbon compounds like enolates or alkenes via double alkylation processes. Commonly employed in the development of active pharmaceutical ingredients where a propionate backbone with reactiv

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its dual bromine functionality allows for selective substitution reactions, making it valuable in constructing complex molecules, including cyclopropane derivatives through reactions with nucleophilic carbon compounds like enolates or alkenes via double alkylation processes. Commonly employed in the development of active pharmaceutical ingredients where a propionate backbone with reactive sites is needed. Also utilized in the synthesis of specialty polymers and functionalized esters for fine chemical applications.

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