(4-Bromobenzyl)hydrazine hydrochloride

95%

Reagent Code: #113309
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CAS Number 1727-08-8

science Other reagents with same CAS 1727-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.52 g/mol
Formula C₇H₁₀BrClN₂
badge Registry Numbers
MDL Number MFCD12031977
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis as a building block for the preparation of various heterocyclic compounds, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the synthesis of hydrazone derivatives, which are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it is employed in the preparation of Schiff bases, which are valuable in coordination chemistry and material science. Its bromo-substituted aromatic ring makes it a versatile reagent for further functionalization through cross-coupling reactions, enabling the creation of complex molecules with tailored properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,125.00
inventory 5g
10-20 days ฿9,810.00
inventory 1g
10-20 days ฿2,808.00

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(4-Bromobenzyl)hydrazine hydrochloride
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This compound is primarily utilized in organic synthesis as a building block for the preparation of various heterocyclic compounds, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the synthesis of hydrazone derivatives, which are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it is employed in the preparation of Schiff bases, which are valuable in coordi

This compound is primarily utilized in organic synthesis as a building block for the preparation of various heterocyclic compounds, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the synthesis of hydrazone derivatives, which are often explored for their potential biological activities, including antimicrobial, anticancer, and anti-inflammatory properties. Additionally, it is employed in the preparation of Schiff bases, which are valuable in coordination chemistry and material science. Its bromo-substituted aromatic ring makes it a versatile reagent for further functionalization through cross-coupling reactions, enabling the creation of complex molecules with tailored properties.

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