7-Methylquinoline-8-sulfonyl chloride

95%

Reagent Code: #210427
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CAS Number 17999-75-6

science Other reagents with same CAS 17999-75-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.69 g/mol
Formula C₁₀H₈ClNO₂S
badge Registry Numbers
MDL Number MFCD18791270
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of fluorescent dyes and probes due to its ability to form stable sulfonamide bonds with amines. Its structure allows for strong UV or visible light absorption, making it valuable in developing sensors for biological molecules. Commonly employed in labeling peptides and proteins for detection in analytical and diagnostic applications. Also utilized in the preparation of sulfa drugs and other bioactive compounds where quinoline derivatives exhibit antimicrobial or antitumor activity. Its sulfonyl chloride group readily reacts with nucleophiles, enabling versatile use in organic synthesis and medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,120.00
inventory 250mg
10-20 days ฿13,550.00
inventory 1g
10-20 days ฿27,100.00
7-Methylquinoline-8-sulfonyl chloride
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Used as a key intermediate in the synthesis of fluorescent dyes and probes due to its ability to form stable sulfonamide bonds with amines. Its structure allows for strong UV or visible light absorption, making it valuable in developing sensors for biological molecules. Commonly employed in labeling peptides and proteins for detection in analytical and diagnostic applications. Also utilized in the preparation of sulfa drugs and other bioactive compounds where quinoline derivatives exhibit antimicrobial o

Used as a key intermediate in the synthesis of fluorescent dyes and probes due to its ability to form stable sulfonamide bonds with amines. Its structure allows for strong UV or visible light absorption, making it valuable in developing sensors for biological molecules. Commonly employed in labeling peptides and proteins for detection in analytical and diagnostic applications. Also utilized in the preparation of sulfa drugs and other bioactive compounds where quinoline derivatives exhibit antimicrobial or antitumor activity. Its sulfonyl chloride group readily reacts with nucleophiles, enabling versatile use in organic synthesis and medicinal chemistry.

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