(2,4-Dimethoxybenzyl)hydrazine hydrochloride

95%

Reagent Code: #178647
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CAS Number 462059-71-8

science Other reagents with same CAS 462059-71-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.68 g/mol
Formula C₉H₁₅ClN₂O₂
badge Registry Numbers
MDL Number MFCD00540455
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. It serves as a building block in the preparation of heterocyclic compounds, particularly in the development of indole and benzodiazepine derivatives, which are common scaffolds in medicinal chemistry. Its hydrazine functionality allows for condensation reactions with carbonyl compounds, enabling the formation of hydrazones—useful intermediates in drug discovery. Also employed in research settings for the modification of bioactive molecules and in the design of novel psychoactive substances, particularly in the synthesis of substituted phenethylamines and tryptamines. Due to its reactivity, it is valuable in organic synthesis for introducing the 2,4-dimethoxybenzyl group as a protecting or directing moiety.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿8,580.00
inventory 1g
10-20 days ฿17,600.00
inventory 5g
10-20 days ฿52,800.00

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(2,4-Dimethoxybenzyl)hydrazine hydrochloride
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Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. It serves as a building block in the preparation of heterocyclic compounds, particularly in the development of indole and benzodiazepine derivatives, which are common scaffolds in medicinal chemistry. Its hydrazine functionality allows for condensation reactions with carbonyl compounds, enabling the formation of hydrazones—useful intermediates in drug discovery. Also employed in research settings for the modifica

Used primarily as a key intermediate in the synthesis of pharmaceuticals and fine chemicals. It serves as a building block in the preparation of heterocyclic compounds, particularly in the development of indole and benzodiazepine derivatives, which are common scaffolds in medicinal chemistry. Its hydrazine functionality allows for condensation reactions with carbonyl compounds, enabling the formation of hydrazones—useful intermediates in drug discovery. Also employed in research settings for the modification of bioactive molecules and in the design of novel psychoactive substances, particularly in the synthesis of substituted phenethylamines and tryptamines. Due to its reactivity, it is valuable in organic synthesis for introducing the 2,4-dimethoxybenzyl group as a protecting or directing moiety.

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