Ethyl cis-3-Bromoacrylate

98%

Reagent Code: #183144
fingerprint
CAS Number 31930-34-4

science Other reagents with same CAS 31930-34-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.01 g/mol
Formula C₅H₇BrO₂
badge Registry Numbers
MDL Number MFCD00674501
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in reactions where a reactive α,β-unsaturated ester system is needed. Its bromine functionality allows for cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in Michael additions and palladium-catalyzed transformations to form carbon-carbon bonds. Also utilized in the preparation of heterocyclic compounds due to its ability to act as a dienophile in cycloaddition reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿3,890.00
inventory 1g
10-20 days ฿9,250.00
inventory 5g
10-20 days ฿29,580.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl cis-3-Bromoacrylate
No image available

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in reactions where a reactive α,β-unsaturated ester system is needed. Its bromine functionality allows for cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in Michael additions and palladium-catalyzed transformations to form carbon-carbon bonds. Also utilized in the preparation of heterocyclic compounds due to its ability to act as a dienophile in cycloadditi

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in reactions where a reactive α,β-unsaturated ester system is needed. Its bromine functionality allows for cross-coupling reactions, making it valuable in building complex organic molecules. Commonly employed in Michael additions and palladium-catalyzed transformations to form carbon-carbon bonds. Also utilized in the preparation of heterocyclic compounds due to its ability to act as a dienophile in cycloaddition reactions.

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...