N-(2-Aminoethyl)benzenesulfonamide hydrochloride

95%

Reagent Code: #219874
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CAS Number 53672-99-4

science Other reagents with same CAS 53672-99-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 236.72 g/mol
Formula C₈H₁₃ClN₂O₂S
badge Registry Numbers
MDL Number MFCD09834110
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting neurological and cardiovascular conditions. Its structure supports the creation of sulfonamide-based drugs, which are known for their antimicrobial and enzyme-inhibiting properties. Also employed in research settings to develop novel ligands for receptor binding studies due to the presence of both amine and sulfonamide functional groups. Additionally, it serves as a building block in the preparation of fluorescent probes and imaging agents, where the amine group can be easily conjugated to dyes or labels. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,460.00
inventory 1g
10-20 days ฿6,810.00
inventory 5g
10-20 days ฿31,900.00
inventory 250mg
10-20 days ฿2,320.00

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N-(2-Aminoethyl)benzenesulfonamide hydrochloride
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Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting neurological and cardiovascular conditions. Its structure supports the creation of sulfonamide-based drugs, which are known for their antimicrobial and enzyme-inhibiting properties. Also employed in research settings to develop novel ligands for receptor binding studies due to the presence of both amine and sulfonamide functional groups. Additionally, it serves as a buil

Used as an intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting neurological and cardiovascular conditions. Its structure supports the creation of sulfonamide-based drugs, which are known for their antimicrobial and enzyme-inhibiting properties. Also employed in research settings to develop novel ligands for receptor binding studies due to the presence of both amine and sulfonamide functional groups. Additionally, it serves as a building block in the preparation of fluorescent probes and imaging agents, where the amine group can be easily conjugated to dyes or labels. Its hydrochloride salt form enhances solubility and stability, making it suitable for use in aqueous reaction systems.

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