tert-Butyl4-bromopent-4-enoate

97%

Reagent Code: #155867
fingerprint
CAS Number 92975-38-7

science Other reagents with same CAS 92975-38-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.12 g/mol
Formula C₉H₁₅BrO₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules through palladium-catalyzed coupling reactions. Its vinyl bromide functionality allows it to participate in cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of carbon-carbon bonds. The tert-butyl ester group provides stability and can be easily deprotected under mild acidic conditions to reveal the corresponding carboxylic acid, making it valuable in multi-step synthesis of pharmaceuticals and natural products. Its structure also lends itself to use in ring-closing metathesis reactions, where the terminal alkene is utilized to form cyclic frameworks. Commonly employed in the development of bioactive compounds and functionalized polymers.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,570.00
inventory 250mg
10-20 days ฿6,180.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl4-bromopent-4-enoate
No image available

Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules through palladium-catalyzed coupling reactions. Its vinyl bromide functionality allows it to participate in cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of carbon-carbon bonds. The tert-butyl ester group provides stability and can be easily deprotected under mild acidic conditions to reveal the corresponding carboxylic acid, making it valuable in multi-step synthes

Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules through palladium-catalyzed coupling reactions. Its vinyl bromide functionality allows it to participate in cross-coupling reactions such as Suzuki or Heck reactions, enabling the construction of carbon-carbon bonds. The tert-butyl ester group provides stability and can be easily deprotected under mild acidic conditions to reveal the corresponding carboxylic acid, making it valuable in multi-step synthesis of pharmaceuticals and natural products. Its structure also lends itself to use in ring-closing metathesis reactions, where the terminal alkene is utilized to form cyclic frameworks. Commonly employed in the development of bioactive compounds and functionalized polymers.

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...