1-Propanesulfonamide N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]

95%

Reagent Code: #39790
fingerprint
CAS Number 1469930-91-3

science Other reagents with same CAS 1469930-91-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 325.23136 g/mol
Formula C₁₅H₂₄BNO₄S
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry and drug development. It serves as a key intermediate in the preparation of biologically active compounds, especially those targeting specific enzymes or receptors. The boronate ester functional group in its structure makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex molecules. Additionally, its sulfonamide moiety can contribute to the development of compounds with potential antibacterial or anti-inflammatory properties. Its applications extend to materials science, where it can be used in the design of advanced polymers or sensors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿83,592.00
inventory 250mg
10-20 days ฿14,292.00
inventory 1g
10-20 days ฿27,792.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Propanesulfonamide N-[3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]
No image available

This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry and drug development. It serves as a key intermediate in the preparation of biologically active compounds, especially those targeting specific enzymes or receptors. The boronate ester functional group in its structure makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex molecules. Additionally, its sulfonamide

This chemical is primarily utilized in organic synthesis, particularly in the field of medicinal chemistry and drug development. It serves as a key intermediate in the preparation of biologically active compounds, especially those targeting specific enzymes or receptors. The boronate ester functional group in its structure makes it valuable for Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds in the synthesis of complex molecules. Additionally, its sulfonamide moiety can contribute to the development of compounds with potential antibacterial or anti-inflammatory properties. Its applications extend to materials science, where it can be used in the design of advanced polymers or sensors.

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...