6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline

97%

Reagent Code: #130560
fingerprint
CAS Number 675576-26-8

science Other reagents with same CAS 675576-26-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.12 g/mol
Formula C₁₅H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD11227091
thermostat Physical Properties
Melting Point 179-184°C
Boiling Point 397.5±15.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex isoquinoline derivatives. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in pharmaceutical research and development. It is commonly employed to construct biaryl systems found in bioactive molecules, including potential drug candidates targeting cancer, inflammation, and central nervous system disorders. Due to its stability and reactivity, it is also utilized in the preparation of organic electronic materials and fluorescent probes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,540.00
inventory 250mg
10-20 days ฿6,030.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline
No image available

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex isoquinoline derivatives. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in pharmaceutical research and development. It is commonly employed to construct biaryl systems found in bioactive molecules, including potential drug candidates targeting cancer, inflammation, and central nervous system disorders. D

Used primarily in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block in the synthesis of complex isoquinoline derivatives. Its boronate ester group enables efficient carbon-carbon bond formation under palladium catalysis, making it valuable in pharmaceutical research and development. It is commonly employed to construct biaryl systems found in bioactive molecules, including potential drug candidates targeting cancer, inflammation, and central nervous system disorders. Due to its stability and reactivity, it is also utilized in the preparation of organic electronic materials and fluorescent probes.

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...