Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarboxylate

97%

Reagent Code: #182455
fingerprint
CAS Number 1049004-32-1

science Other reagents with same CAS 1049004-32-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.17 g/mol
Formula C₁₅H₂₅BO₄
thermostat Physical Properties
Boiling Point 312.6±52.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for forming carbon-carbon bonds in organic synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in the preparation of complex organic molecules, particularly in pharmaceutical and agrochemical research. The presence of a cyclohexene ring with an ester functionality allows for further structural modifications, enabling the synthesis of diverse cyclic compounds. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,920.00
inventory 5g
10-20 days ฿7,680.00
inventory 25g
10-20 days ฿28,800.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)cyclohex-3-enecarboxylate
No image available

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for forming carbon-carbon bonds in organic synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in the preparation of complex organic molecules, particularly in pharmaceutical and agrochemical research. The presence of a cyclohexene ring with an ester functionality allows for further structural modifications, enabling the

Widely used in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for forming carbon-carbon bonds in organic synthesis. Its boronate ester group readily participates in palladium-catalyzed couplings with aryl or vinyl halides, making it valuable in the preparation of complex organic molecules, particularly in pharmaceutical and agrochemical research. The presence of a cyclohexene ring with an ester functionality allows for further structural modifications, enabling the synthesis of diverse cyclic compounds. Its stability and reactivity profile make it suitable for use in late-stage functionalization during drug discovery and development.

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...