4-Methyl-N'-(1-phenylbutylidene)benzenesulfonohydrazide

98%

Reagent Code: #215764
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CAS Number 41780-81-8

science Other reagents with same CAS 41780-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.42 g/mol
Formula C₁₇H₂₀N₂O₂S
badge Registry Numbers
MDL Number MFCD01230699
thermostat Physical Properties
Melting Point 122-125 °C(lit.)
Boiling Point 459.9±38.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. It serves as a key building block in the preparation of bioactive molecules due to its hydrazide functionality, which can undergo cyclization and condensation reactions to form heterocyclic compounds. Commonly employed in the synthesis of sulfonamide-based drugs, where it contributes to enhanced metabolic stability and target binding. Also utilized in research settings for designing novel hydrazone derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Its structural features make it suitable for Schiff base formation, enabling applications in coordination chemistry and catalyst design.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿3,410.00
5g
10-20 days ฿11,930.00
4-Methyl-N'-(1-phenylbutylidene)benzenesulfonohydrazide
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Used primarily as an intermediate in organic synthesis, especially in the development of pharmaceuticals and agrochemicals. It serves as a key building block in the preparation of bioactive molecules due to its hydrazide functionality, which can undergo cyclization and condensation reactions to form heterocyclic compounds. Commonly employed in the synthesis of sulfonamide-based drugs, where it contributes to enhanced metabolic stability and target binding. Also utilized in research settings for designing novel hydrazone derivatives with potential antimicrobial, anti-inflammatory, or anticancer properties. Its structural features make it suitable for Schiff base formation, enabling applications in coordination chemistry and catalyst design.
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