(E)-tert-Butyl 2-benzylidenehydrazinecarboxylate

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Reagent Code: #182695
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CAS Number 24469-50-9

science Other reagents with same CAS 24469-50-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.27 g/mol
Formula C₁₂H₁₆N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and agrochemicals. It serves as a building block in the formation of heterocyclic compounds, including pyrazoles and triazoles, which are common scaffolds in drug discovery. Its structure allows for selective reactions in condensation and cyclization processes, making it valuable in developing bioactive molecules. Also employed in research settings for the synthesis of novel Schiff bases with potential antimicrobial or anticancer properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,340.00
inventory 1g
10-20 days ฿6,330.00
inventory 5g
10-20 days ฿19,580.00
inventory 25g
10-20 days ฿63,040.00
inventory 10g
10-20 days ฿31,820.00
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(E)-tert-Butyl 2-benzylidenehydrazinecarboxylate
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Used as an intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and agrochemicals. It serves as a building block in the formation of heterocyclic compounds, including pyrazoles and triazoles, which are common scaffolds in drug discovery. Its structure allows for selective reactions in condensation and cyclization processes, making it valuable in developing bioactive molecules. Also employed in research settings for the synthesis of novel Schiff bases with

Used as an intermediate in organic synthesis, particularly in the preparation of hydrazine-based pharmaceuticals and agrochemicals. It serves as a building block in the formation of heterocyclic compounds, including pyrazoles and triazoles, which are common scaffolds in drug discovery. Its structure allows for selective reactions in condensation and cyclization processes, making it valuable in developing bioactive molecules. Also employed in research settings for the synthesis of novel Schiff bases with potential antimicrobial or anticancer properties.

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