2-Amino-5-fluoro-N-phenylbenzamide

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Reagent Code: #137017
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CAS Number 60041-89-6

science Other reagents with same CAS 60041-89-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.24 g/mol
Formula C₁₃H₁₁FN₂O
badge Registry Numbers
MDL Number MFCD11101521
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Shows utility in medicinal chemistry for constructing bioactive molecules due to the presence of both amine and amide functional groups, which facilitate peptide-like coupling. The fluorine atom enhances binding selectivity and metabolic stability in drug candidates. Also employed in the preparation of fluorescent probes for biochemical assays, leveraging the electron-withdrawing fluorine and aromatic system for optical properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿620.00
inventory 1g
10-20 days ฿1,570.00

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2-Amino-5-fluoro-N-phenylbenzamide
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Used as an intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Shows utility in medicinal chemistry for constructing bioactive molecules due to the presence of both amine and amide functional groups, which facilitate peptide-like coupling. The fluorine atom enhances binding selectivity and metabolic stability in drug candidates. Also employed in the preparation of fluorescent probes for biochemical assays, leveraging the

Used as an intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Shows utility in medicinal chemistry for constructing bioactive molecules due to the presence of both amine and amide functional groups, which facilitate peptide-like coupling. The fluorine atom enhances binding selectivity and metabolic stability in drug candidates. Also employed in the preparation of fluorescent probes for biochemical assays, leveraging the electron-withdrawing fluorine and aromatic system for optical properties.

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