(3-bromo-2-methylprop-1-enyl)benzene

95%

Reagent Code: #141565
fingerprint
CAS Number 79655-52-0

science Other reagents with same CAS 79655-52-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 211.1 g/mol
Formula C₁₀H₁₁Br
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. The bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic and alkenyl systems. The vinyl bromide moiety is particularly useful in forming carbon-carbon bonds under palladium catalysis. Its styrenyl structure with a brominated alkene side chain makes it suitable for polymer modification and development of specialty materials. Also employed in the synthesis of bioactive molecules where the bromine serves as a leaving group or a site for further functionalization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿22,500.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(3-bromo-2-methylprop-1-enyl)benzene
No image available

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. The bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic and alkenyl systems. The vinyl bromide moiety is particularly useful in forming carbon-carbon bonds under palladium catalysis. Its styrenyl structure with a brominated alkene side chain makes it suitable for polymer modification and development of specialty materials. Also employed

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. The bromine functionality allows for cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic and alkenyl systems. The vinyl bromide moiety is particularly useful in forming carbon-carbon bonds under palladium catalysis. Its styrenyl structure with a brominated alkene side chain makes it suitable for polymer modification and development of specialty materials. Also employed in the synthesis of bioactive molecules where the bromine serves as a leaving group or a site for further functionalization.

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...