N'-Phenylbenzohydrazonoyl chloride

95%

Reagent Code: #220257
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CAS Number 15424-14-3

science Other reagents with same CAS 15424-14-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.69 g/mol
Formula C₁₃H₁₁ClN₂
badge Registry Numbers
MDL Number MFCD00180187
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of five- and six-membered rings such as pyrazoles and isoxazoles. It participates in cyclocondensation reactions with nucleophiles like enolates, amines, and hydrazines, enabling the construction of complex aromatic systems found in pharmaceuticals and agrochemicals. Its reactivity as an electrophilic hydrazonoyl chloride makes it valuable in forming carbon–nitrogen and carbon–carbon bonds under mild conditions. Commonly employed in research settings for developing bioactive molecules and functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿7,640.00
N'-Phenylbenzohydrazonoyl chloride
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Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of five- and six-membered rings such as pyrazoles and isoxazoles. It participates in cyclocondensation reactions with nucleophiles like enolates, amines, and hydrazines, enabling the construction of complex aromatic systems found in pharmaceuticals and agrochemicals. Its reactivity as an electrophilic hydrazonoyl chloride makes it valuable in forming carbon–nitrogen and carbon–carbon bonds under mild co

Used as a key intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of five- and six-membered rings such as pyrazoles and isoxazoles. It participates in cyclocondensation reactions with nucleophiles like enolates, amines, and hydrazines, enabling the construction of complex aromatic systems found in pharmaceuticals and agrochemicals. Its reactivity as an electrophilic hydrazonoyl chloride makes it valuable in forming carbon–nitrogen and carbon–carbon bonds under mild conditions. Commonly employed in research settings for developing bioactive molecules and functional materials.

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