(2-(N-(tert-Butyl)sulfamoyl)-5-isobutylthiophen-3-yl)boronic acid

95%

Reagent Code: #220752
fingerprint
CAS Number 163520-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.25 g/mol
Formula C₁₂H₂₂BNO₄S₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a boronic acid reagent for constructing biaryl compounds in medicinal chemistry. Its structure enables selective coupling under mild conditions, making it valuable in synthesizing drug candidates targeting inflammation and central nervous system disorders. The sulfamoyl and thiophene groups enhance stability and electronic properties, improving reaction efficiency and selectivity. Commonly applied in late-stage functionalization of complex molecules in pharmaceutical development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,550.00
inventory 250mg
10-20 days ฿7,760.00
inventory 1g
10-20 days ฿22,600.00
(2-(N-(tert-Butyl)sulfamoyl)-5-isobutylthiophen-3-yl)boronic acid
Used in Suzuki-Miyaura cross-coupling reactions as a boronic acid reagent for constructing biaryl compounds in medicinal chemistry. Its structure enables selective coupling under mild conditions, making it valuable in synthesizing drug candidates targeting inflammation and central nervous system disorders. The sulfamoyl and thiophene groups enhance stability and electronic properties, improving reaction efficiency and selectivity. Commonly applied in late-stage functionalization of complex molecules in pharmaceutical 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...

Cart

No products

Subtotal: ฿0.00
Total ฿0.00 THB