3-Ethoxybenzohydrazide

95%

Reagent Code: #184409
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CAS Number 27830-16-6

science Other reagents with same CAS 27830-16-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 180.20 g/mol
Formula C₉H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD00017063
thermostat Physical Properties
Melting Point 101 °C
inventory_2 Storage & Handling
Density 1.144±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antitubercular and antimicrobial agents. It serves as a key building block in the preparation of heterocyclic derivatives such as oxadiazoles and triazoles, which exhibit biological activity. Also employed in agrochemical research for designing novel plant protection agents. Its hydrazide functionality allows for easy derivatization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,740.00
inventory 1g
10-20 days ฿4,120.00
inventory 5g
10-20 days ฿15,850.00

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3-Ethoxybenzohydrazide
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antitubercular and antimicrobial agents. It serves as a key building block in the preparation of heterocyclic derivatives such as oxadiazoles and triazoles, which exhibit biological activity. Also employed in agrochemical research for designing novel plant protection agents. Its hydrazide functionality allows for easy derivatization, making it valuable in medicinal chemistry for structure-activity rel

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antitubercular and antimicrobial agents. It serves as a key building block in the preparation of heterocyclic derivatives such as oxadiazoles and triazoles, which exhibit biological activity. Also employed in agrochemical research for designing novel plant protection agents. Its hydrazide functionality allows for easy derivatization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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