4-(2-Aminoethyl)benzenesulfonamide

99%

Reagent Code: #110609
label
Alias 4-(2-aminoethyl)benzenesulfonamide
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CAS Number 35303-76-5

science Other reagents with same CAS 35303-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.26 g/mol
Formula H₂NCH₂CH₂C₆H₄SO₂NH₂
badge Registry Numbers
EC Number 252-501-0
MDL Number MFCD00010301
thermostat Physical Properties
Melting Point 150-152 °C(lit.)
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various sulfonamide-based drugs, which are widely used as antibiotics, diuretics, and anti-inflammatory agents. Its structure allows for modifications that can enhance the efficacy and specificity of the resulting drugs. Additionally, it is employed in biochemical studies to investigate enzyme inhibition mechanisms, particularly those involving carbonic anhydrase, due to its sulfonamide functional group. Its applications also extend to the development of diagnostic agents and in the study of cellular processes related to ion transport and pH regulation.

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Test Parameter Specification
Loss on Drying 0-1.5
Melting Point 145-150
Purity 99-100%
Water (Karl Fischer) 0-1
Appearance White to yellow crystals or powder or crystalline powder
Infrared Spectrum Conforms To Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿580.00
inventory 100g
10-20 days ฿2,200.00
inventory 500g
10-20 days ฿10,120.00

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4-(2-Aminoethyl)benzenesulfonamide
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various sulfonamide-based drugs, which are widely used as antibiotics, diuretics, and anti-inflammatory agents. Its structure allows for modifications that can enhance the efficacy and specificity of the resulting drugs. Additionally, it is employed in biochemical studies to investigate enzyme inhibition mechanisms, particularly those involving carbonic

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various sulfonamide-based drugs, which are widely used as antibiotics, diuretics, and anti-inflammatory agents. Its structure allows for modifications that can enhance the efficacy and specificity of the resulting drugs. Additionally, it is employed in biochemical studies to investigate enzyme inhibition mechanisms, particularly those involving carbonic anhydrase, due to its sulfonamide functional group. Its applications also extend to the development of diagnostic agents and in the study of cellular processes related to ion transport and pH regulation.

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