1,4-Benzodioxane-6-boronic acid

97%

Reagent Code: #144584
fingerprint
CAS Number 164014-95-3

science Other reagents with same CAS 164014-95-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.97 g/mol
Formula C₈H₉BO₄
badge Registry Numbers
MDL Number MFCD01009696
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of bioactive molecules. Commonly employed in the preparation of drug intermediates where the benzodioxane scaffold is present, contributing to improved metabolic stability and binding affinity in target compounds. Also utilized in materials science for constructing functional organic frameworks and conjugated systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿144.00
inventory 5g
10-20 days ฿1,570.00
inventory 25g
10-20 days ฿7,690.00
inventory 1g
10-20 days ฿380.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1,4-Benzodioxane-6-boronic acid
No image available

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of bioactive molecules. Commonly employed in the preparation of drug intermediates where the benzodioxane scaffold is present, contributing to improved metabolic stability and binding affinity in target compounds. Also utilized in m

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of bioactive molecules. Commonly employed in the preparation of drug intermediates where the benzodioxane scaffold is present, contributing to improved metabolic stability and binding affinity in target compounds. Also utilized in materials science for constructing functional organic frameworks and conjugated systems.

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...