N-(2-Bromophenyl)quinoline-8-sulfonamide

98%

Reagent Code: #215565
fingerprint
CAS Number 326914-66-3

science Other reagents with same CAS 326914-66-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.23 g/mol
Formula C₁₅H₁₁BrN₂O₂S
thermostat Physical Properties
Boiling Point 520.1±56.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.635±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting kinase inhibition. Its structure supports the development of selective inhibitors for protein kinases involved in cellular signaling pathways, making it valuable in cancer research and anti-inflammatory drug design. The compound’s sulfonamide linkage and aromatic framework enhance binding affinity to enzyme active sites. Additionally, it serves as a building block in medicinal chemistry for optimizing drug candidates due to its favorable electronic and steric properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,200.00
inventory 250mg
10-20 days ฿20,750.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
N-(2-Bromophenyl)quinoline-8-sulfonamide
No image available
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting kinase inhibition. Its structure supports the development of selective inhibitors for protein kinases involved in cellular signaling pathways, making it valuable in cancer research and anti-inflammatory drug design. The compound’s sulfonamide linkage and aromatic framework enhance binding affinity to enzyme active sites. Additionally, it serves as a building block in medicinal chemistry fo
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting kinase inhibition. Its structure supports the development of selective inhibitors for protein kinases involved in cellular signaling pathways, making it valuable in cancer research and anti-inflammatory drug design. The compound’s sulfonamide linkage and aromatic framework enhance binding affinity to enzyme active sites. Additionally, it serves as a building block in medicinal chemistry for optimizing drug candidates due to its favorable electronic and steric 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...