(4-Isobutyramidophenyl)boronic acid

98%

Reagent Code: #200918
fingerprint
CAS Number 874219-50-8

science Other reagents with same CAS 874219-50-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.04 g/mol
Formula C₁₀H₁₄BNO₃
badge Registry Numbers
MDL Number MFCD08235068
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of proteasome inhibitors like bortezomib, which is employed in cancer therapy. Its boronic acid functional group enables reversible interactions with biological targets containing diols or active serine residues, making it valuable in medicinal chemistry. Also utilized in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks in drug discovery and in the design of sensors for carbohydrates due to its affinity for diol-containing molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿4,270.00
inventory 1g
10-20 days ฿11,500.00
inventory 5g
10-20 days ฿40,250.00

Cart

No products

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

Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of proteasome inhibitors like bortezomib, which is employed in cancer therapy. Its boronic acid functional group enables reversible interactions with biological targets containing diols or active serine residues, making it valuable in medicinal chemistry. Also utilized in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks in drug discovery and in the design of sensors for carbohydrates d

Used in organic synthesis as a building block for pharmaceuticals, particularly in the development of proteasome inhibitors like bortezomib, which is employed in cancer therapy. Its boronic acid functional group enables reversible interactions with biological targets containing diols or active serine residues, making it valuable in medicinal chemistry. Also utilized in Suzuki-Miyaura cross-coupling reactions to construct biaryl frameworks in drug discovery and in the design of sensors for carbohydrates due to its affinity for diol-containing molecules.

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...