[5-(dimethylsulfamoyl)-2-methylphenyl]boronic acid

98%

Reagent Code: #179204
fingerprint
CAS Number 871332-99-9

science Other reagents with same CAS 871332-99-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 243.09 g/mol
Formula C₉H₁₄BNO₄S
badge Registry Numbers
MDL Number MFCD08056363
thermostat Physical Properties
Melting Point 86-92 °C
Boiling Point 440.7 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.33±0.1 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used in Suzuki-Miyaura cross-coupling reactions as a key building block for synthesizing biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The dimethylsulfamoyl group enhances solubility and directs regioselectivity during coupling, improving reaction yields. Commonly employed in the development of drug candidates targeting enzymes and receptors due to its stability and functional group compatibility. Also utilized in materials science for constructing conjugated organic frameworks with electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,240.00
inventory 1g
10-20 days ฿12,000.00
inventory 5g
10-20 days ฿55,990.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
[5-(dimethylsulfamoyl)-2-methylphenyl]boronic acid
No image available

Used in Suzuki-Miyaura cross-coupling reactions as a key building block for synthesizing biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The dimethylsulfamoyl group enhances solubility and directs regioselectivity during coupling, improving reaction yields. Commonly employed in the development of drug candidates targeting enzymes and receptors due to its stability and functional group compatibility.

Used in Suzuki-Miyaura cross-coupling reactions as a key building block for synthesizing biaryl compounds in pharmaceutical and agrochemical research. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. The dimethylsulfamoyl group enhances solubility and directs regioselectivity during coupling, improving reaction yields. Commonly employed in the development of drug candidates targeting enzymes and receptors due to its stability and functional group compatibility. Also utilized in materials science for constructing conjugated organic frameworks with electronic properties.

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...