(3-Bromo-4-chlorophenyl)hydrazinehydrochloride

98%

Reagent Code: #155676
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CAS Number 1172589-41-1

science Other reagents with same CAS 1172589-41-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.94 g/mol
Formula C₆H₇BrCl₂N₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of heterocyclic compounds, particularly in the formation of indoles and other nitrogen-containing rings through cyclization reactions. Its hydrazine functionality allows it to participate in diazotization and coupling reactions, useful in dye and pigment manufacturing. Also employed in research settings for the development of novel bioactive molecules, including potential antitumor and antimicrobial agents. The hydrochloride salt form enhances stability and solubility, facilitating handling and reaction in aqueous or polar organic media.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,920.00
inventory 1g
10-20 days ฿42,560.00
inventory 100mg
10-20 days ฿9,740.00

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(3-Bromo-4-chlorophenyl)hydrazinehydrochloride
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of heterocyclic compounds, particularly in the formation of indoles and other nitrogen-containing rings through cyclization reactions. Its hydrazine functionality allows it to participate in diazotization and coupling reactions, useful in dye and pigment manufacturing. Also employed in research settings for the development of novel bioactive molecules, including potent

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. It serves as a building block in the preparation of heterocyclic compounds, particularly in the formation of indoles and other nitrogen-containing rings through cyclization reactions. Its hydrazine functionality allows it to participate in diazotization and coupling reactions, useful in dye and pigment manufacturing. Also employed in research settings for the development of novel bioactive molecules, including potential antitumor and antimicrobial agents. The hydrochloride salt form enhances stability and solubility, facilitating handling and reaction in aqueous or polar organic media.

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