Pyridine-3-sulfonyl chloride hydrochloride

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Reagent Code: #227196
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Alias 3-pyridinesulfonyl chloride hydrochloride
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CAS Number 42899-76-3

science Other reagents with same CAS 42899-76-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 214.07 g/mol
Formula C₅H₅ClNO₂S
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MDL Number MFCD04035552
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a key reagent in organic synthesis, particularly in the preparation of sulfonamides, which are important in pharmaceutical development. It readily reacts with amines to form pyridine-3-sulfonamide derivatives, many of which exhibit biological activity, including antimicrobial and antiviral properties. Commonly employed in medicinal chemistry for modifying drug candidates to enhance solubility, stability, and target binding affinity. Also utilized in agrochemical synthesis and as a derivatizing agent in analytical chemistry for detection of amine-containing compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿990.00
inventory 1g
10-20 days ฿3,560.00
inventory 5g
10-20 days ฿9,200.00
inventory 25g
10-20 days ฿15,470.00

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Pyridine-3-sulfonyl chloride hydrochloride
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Used as a key reagent in organic synthesis, particularly in the preparation of sulfonamides, which are important in pharmaceutical development. It readily reacts with amines to form pyridine-3-sulfonamide derivatives, many of which exhibit biological activity, including antimicrobial and antiviral properties. Commonly employed in medicinal chemistry for modifying drug candidates to enhance solubility, stability, and target binding affinity. Also utilized in agrochemical synthesis and as a derivatizing agent
Used as a key reagent in organic synthesis, particularly in the preparation of sulfonamides, which are important in pharmaceutical development. It readily reacts with amines to form pyridine-3-sulfonamide derivatives, many of which exhibit biological activity, including antimicrobial and antiviral properties. Commonly employed in medicinal chemistry for modifying drug candidates to enhance solubility, stability, and target binding affinity. Also utilized in agrochemical synthesis and as a derivatizing agent in analytical chemistry for detection of amine-containing compounds.
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