2-Amino-N-(2-fluorophenyl)benzamide

95%

Reagent Code: #215791
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CAS Number 39511-95-0

science Other reagents with same CAS 39511-95-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.24 g/mol
Formula C₁₃H₁₁FN₂O
badge Registry Numbers
MDL Number MFCD03180260
thermostat Physical Properties
Melting Point 123-125 °C(Solv: benzene (71-43-2))
Boiling Point 302.4±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.317±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research. It serves as a building block for compounds with potential anticonvulsant, anti-inflammatory, and antimicrobial activities. Its structure supports the development of kinase inhibitors and other targeted therapies in medicinal chemistry. Also employed in the preparation of fluorescent probes due to its amide and aromatic amine functionalities, which can enhance binding and detection in biological systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,960.00
inventory 250mg
10-20 days ฿11,830.00

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2-Amino-N-(2-fluorophenyl)benzamide
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Used as an intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research. It serves as a building block for compounds with potential anticonvulsant, anti-inflammatory, and antimicrobial activities. Its structure supports the development of kinase inhibitors and other targeted therapies in medicinal chemistry. Also employed in the preparation of fluorescent probes due to its amide and aromatic amine functionalities, which can enhance binding and detection in biological syst

Used as an intermediate in the synthesis of bioactive molecules, particularly in pharmaceutical research. It serves as a building block for compounds with potential anticonvulsant, anti-inflammatory, and antimicrobial activities. Its structure supports the development of kinase inhibitors and other targeted therapies in medicinal chemistry. Also employed in the preparation of fluorescent probes due to its amide and aromatic amine functionalities, which can enhance binding and detection in biological systems.

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