N-(3-fluorophenyl)hydrazinecarboxamide

95%

Reagent Code: #219174
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CAS Number 114670-74-5

science Other reagents with same CAS 114670-74-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 169.16 g/mol
Formula C₇H₈FN₃O
badge Registry Numbers
MDL Number MFCD00040977
thermostat Physical Properties
Melting Point 133-135 °C
inventory_2 Storage & Handling
Density 1.378±0.06 g/cm3(Predicted)
Storage Room temperature

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 building block in heterocyclic chemistry, facilitating the formation of fused ring systems like triazoles and pyridazines. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate bioavailability and binding affinity. Also utilized in the preparation of hydrazide-based inhibitors targeting specific enzymes in pathogenic organisms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,550.00
inventory 250mg
10-20 days ฿11,150.00
inventory 1g
10-20 days ฿27,600.00

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N-(3-fluorophenyl)hydrazinecarboxamide
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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 building block in heterocyclic chemistry, facilitating the formation of fused ring systems like triazoles and pyridazines. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate bioavailability and binding affinity. Also utilized in the preparation of hydrazide-based inhibitors ta

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of antitubercular and antimicrobial agents. It serves as a building block in heterocyclic chemistry, facilitating the formation of fused ring systems like triazoles and pyridazines. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies due to its ability to modulate bioavailability and binding affinity. Also utilized in the preparation of hydrazide-based inhibitors targeting specific enzymes in pathogenic organisms.

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