2-Naphthalenesulfonyl chloride

98%

Reagent Code: #216999
label
Alias β-naphthalenesulfonyl chloride;naphthalene-2-sulfonyl chloride
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CAS Number 93-11-8

science Other reagents with same CAS 93-11-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.67 g/mol
Formula C₁₀H₇ClO₂S
badge Registry Numbers
MDL Number MFCD00004087
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Widely used in organic synthesis, particularly as a derivatizing agent for amines and amino acids. It reacts selectively with primary and secondary amines to form sulfonamides, which are useful intermediates in pharmaceutical manufacturing and analytical chemistry. Commonly employed in the preparation of fluorescent probes and tags due to the naphthalene ring’s inherent fluorescence properties. Also serves as a precursor in the synthesis of dyes, agrochemicals, and certain protease inhibitors. Its reactivity makes it valuable in peptide chemistry for protecting group strategies and in the development of enzyme inhibitors where sulfonyl groups enhance binding affinity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿690.00
inventory 100g
10-20 days ฿2,200.00
2-Naphthalenesulfonyl chloride
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Widely used in organic synthesis, particularly as a derivatizing agent for amines and amino acids. It reacts selectively with primary and secondary amines to form sulfonamides, which are useful intermediates in pharmaceutical manufacturing and analytical chemistry. Commonly employed in the preparation of fluorescent probes and tags due to the naphthalene ring’s inherent fluorescence properties. Also serves as a precursor in the synthesis of dyes, agrochemicals, and certain protease inhibitors. Its reacti

Widely used in organic synthesis, particularly as a derivatizing agent for amines and amino acids. It reacts selectively with primary and secondary amines to form sulfonamides, which are useful intermediates in pharmaceutical manufacturing and analytical chemistry. Commonly employed in the preparation of fluorescent probes and tags due to the naphthalene ring’s inherent fluorescence properties. Also serves as a precursor in the synthesis of dyes, agrochemicals, and certain protease inhibitors. Its reactivity makes it valuable in peptide chemistry for protecting group strategies and in the development of enzyme inhibitors where sulfonyl groups enhance binding affinity.

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