N'-(p-Tolyl)acetohydrazide

95%

Reagent Code: #214798
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CAS Number 61700-79-6

science Other reagents with same CAS 61700-79-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.2 g/mol
Formula C₉H₁₂N₂O
badge Registry Numbers
MDL Number MFCD01221067
inventory_2 Storage & Handling
Storage Room temperature, inert gas

description Product Description

Used as an intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of oxadiazoles and other nitrogen-containing rings which exhibit biological activity. Commonly applied in medicinal chemistry for developing antimicrobial, anti-inflammatory, and antitubercular agents. Also utilized in the design of hydrazide-based inhibitors targeting specific enzymes due to its ability to form stable conjugates. Its aromatic and polar functional groups make it suitable for enhancing binding affinity in drug design.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,460.00
inventory 1g
10-20 days ฿6,660.00
inventory 5g
10-20 days ฿23,270.00

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N'-(p-Tolyl)acetohydrazide
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Used as an intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of oxadiazoles and other nitrogen-containing rings which exhibit biological activity. Commonly applied in medicinal chemistry for developing antimicrobial, anti-inflammatory, and antitubercular agents. Also utilized in the design of hydrazide-based inhibitors targeting specific enzymes due to its ability to form stable conjugates. Its aromatic and polar functional groups make it suitable for enhancing bind

Used as an intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of oxadiazoles and other nitrogen-containing rings which exhibit biological activity. Commonly applied in medicinal chemistry for developing antimicrobial, anti-inflammatory, and antitubercular agents. Also utilized in the design of hydrazide-based inhibitors targeting specific enzymes due to its ability to form stable conjugates. Its aromatic and polar functional groups make it suitable for enhancing binding affinity in drug design.

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