3-Hydrazino-benzoicacidethylester

98%

Reagent Code: #196754
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CAS Number 90556-87-9

science Other reagents with same CAS 90556-87-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.20 g/mol
Formula C₉H₁₂N₂O₂
thermostat Physical Properties
Melting Point 330.4 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of pharmaceuticals and agrochemicals. Its hydrazine functionality allows it to participate in cyclization reactions, forming pyrazole, triazole, or other nitrogen-containing rings that are common in bioactive molecules. It is also employed in the development of dyes and functional materials due to its ability to undergo condensation and coupling reactions. Its ester group enables further derivatization, making it valuable in combinatorial chemistry and drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿36,400.00
3-Hydrazino-benzoicacidethylester
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Used as an intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of pharmaceuticals and agrochemicals. Its hydrazine functionality allows it to participate in cyclization reactions, forming pyrazole, triazole, or other nitrogen-containing rings that are common in bioactive molecules. It is also employed in the development of dyes and functional materials due to its ability to undergo condensation and coupling reactions. Its ester group enables further derivatization, ma

Used as an intermediate in the synthesis of heterocyclic compounds, particularly in the preparation of pharmaceuticals and agrochemicals. Its hydrazine functionality allows it to participate in cyclization reactions, forming pyrazole, triazole, or other nitrogen-containing rings that are common in bioactive molecules. It is also employed in the development of dyes and functional materials due to its ability to undergo condensation and coupling reactions. Its ester group enables further derivatization, making it valuable in combinatorial chemistry and drug discovery.

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