N'-(1-(Benzo[d][1,3]dioxol-5-yl)ethylidene)-4-methylbenzenesulfonohydrazide

95%

Reagent Code: #219362
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CAS Number 401595-24-2

science Other reagents with same CAS 401595-24-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.37 g/mol
Formula C₁₆H₁₆N₂O₄S
inventory_2 Storage & Handling
Storage 2-8°C, Inert gas storage

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of bioactive compounds and pharmaceuticals. Its structure supports the formation of hydrazone derivatives, which are valuable in medicinal chemistry for their antimicrobial, antifungal, and anticancer properties. Commonly employed in research settings to design novel heterocyclic compounds with potential therapeutic activity. Also utilized in the preparation of sulfonamide-based agents, known for their enzyme inhibitory effects. Suitable for use in condensation reactions to build complex molecular frameworks in drug discovery.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿880.00
inventory 1g
10-20 days ฿2,330.00
inventory 5g
10-20 days ฿8,380.00
N'-(1-(Benzo[d][1,3]dioxol-5-yl)ethylidene)-4-methylbenzenesulfonohydrazide
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Used as an intermediate in organic synthesis, particularly in the development of bioactive compounds and pharmaceuticals. Its structure supports the formation of hydrazone derivatives, which are valuable in medicinal chemistry for their antimicrobial, antifungal, and anticancer properties. Commonly employed in research settings to design novel heterocyclic compounds with potential therapeutic activity. Also utilized in the preparation of sulfonamide-based agents, known for their enzyme inhibitory effects

Used as an intermediate in organic synthesis, particularly in the development of bioactive compounds and pharmaceuticals. Its structure supports the formation of hydrazone derivatives, which are valuable in medicinal chemistry for their antimicrobial, antifungal, and anticancer properties. Commonly employed in research settings to design novel heterocyclic compounds with potential therapeutic activity. Also utilized in the preparation of sulfonamide-based agents, known for their enzyme inhibitory effects. Suitable for use in condensation reactions to build complex molecular frameworks in drug discovery.

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