5-(Aminomethyl)Thiophene-2-Sulfonamide Hydrochloride

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Reagent Code: #138769
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CAS Number 21151-36-0

science Other reagents with same CAS 21151-36-0

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Weight 228.72 g/mol
Formula C₅H₉ClN₂O₂S₂
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Storage Room temperature

description Product Description

Used primarily in pharmaceutical synthesis, this compound serves as a key intermediate in the development of sulfonamide-based drugs. Its structure supports the creation of bioactive molecules with potential antidiabetic, antimicrobial, and anti-inflammatory properties. The aminomethyl group enables coupling reactions in medicinal chemistry, facilitating the construction of more complex drug candidates. It is also employed in research settings to design enzyme inhibitors, particularly targeting carbonic anhydrase due to the sulfonamide functionality. Its hydrochloride salt form improves solubility and stability, making it suitable for use in aqueous reaction systems and biological assays.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿6,510.00
inventory 1g
10-20 days ฿22,870.00

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5-(Aminomethyl)Thiophene-2-Sulfonamide Hydrochloride
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Used primarily in pharmaceutical synthesis, this compound serves as a key intermediate in the development of sulfonamide-based drugs. Its structure supports the creation of bioactive molecules with potential antidiabetic, antimicrobial, and anti-inflammatory properties. The aminomethyl group enables coupling reactions in medicinal chemistry, facilitating the construction of more complex drug candidates. It is also employed in research settings to design enzyme inhibitors, particularly targeting carbonic

Used primarily in pharmaceutical synthesis, this compound serves as a key intermediate in the development of sulfonamide-based drugs. Its structure supports the creation of bioactive molecules with potential antidiabetic, antimicrobial, and anti-inflammatory properties. The aminomethyl group enables coupling reactions in medicinal chemistry, facilitating the construction of more complex drug candidates. It is also employed in research settings to design enzyme inhibitors, particularly targeting carbonic anhydrase due to the sulfonamide functionality. Its hydrochloride salt form improves solubility and stability, making it suitable for use in aqueous reaction systems and biological assays.

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