(4-Bromobutyl)boronic acid

95%

Reagent Code: #155876
fingerprint
CAS Number 61632-72-2

science Other reagents with same CAS 61632-72-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.837 g/mol
Formula C₄H₁₀BBrO₂
thermostat Physical Properties
Melting Point 73-83 °C
Boiling Point 283.2±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.450±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used primarily in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its bromo and boronic acid functional groups allow dual reactivity, making it valuable for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. The compound serves as a versatile linker in the design of bioactive compounds and functional materials where controlled molecular extension is required. Its reactivity profile supports the development of intermediates in drug discovery and polymer chemistry.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,960.00
inventory 1g
10-20 days ฿16,750.00
inventory 5g
10-20 days ฿68,400.00
inventory 100mg
10-20 days ฿3,660.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(4-Bromobutyl)boronic acid
No image available

Used primarily in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its bromo and boronic acid functional groups allow dual reactivity, making it valuable for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. The compound serves as a versatile linker in the design of bioactive compounds and functional materials where controlled molecular extension is required. Its reactivity profi

Used primarily in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its bromo and boronic acid functional groups allow dual reactivity, making it valuable for constructing complex organic molecules, especially in pharmaceutical and agrochemical research. The compound serves as a versatile linker in the design of bioactive compounds and functional materials where controlled molecular extension is required. Its reactivity profile supports the development of intermediates in drug discovery and polymer chemistry.

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...