N-(4-Methoxyphenyl)Benzenesulfonamide

98%

Reagent Code: #220084
fingerprint
CAS Number 7471-26-3

science Other reagents with same CAS 7471-26-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.31 g/mol
Formula C₁₃H₁₃NO₃S
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide-based compounds, which are known for their biological activity. Commonly employed in the design of enzyme inhibitors due to the sulfonamide group's ability to interact with active sites. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates. Its methoxyphenyl moiety can enhance lipophilicity and influence metabolic stability in drug molecules.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,750.00
N-(4-Methoxyphenyl)Benzenesulfonamide
No image available

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide-based compounds, which are known for their biological activity. Commonly employed in the design of enzyme inhibitors due to the sulfonamide group's ability to interact with active sites. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates. Its methoxyphenyl mo

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of sulfonamide-based compounds, which are known for their biological activity. Commonly employed in the design of enzyme inhibitors due to the sulfonamide group's ability to interact with active sites. Also utilized in medicinal chemistry for structure-activity relationship (SAR) studies, helping optimize drug candidates. Its methoxyphenyl moiety can enhance lipophilicity and influence metabolic stability in drug 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...