2-Phenoxypyridin-4-amine

≥95%

Reagent Code: #226365
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CAS Number 21203-83-8

science Other reagents with same CAS 21203-83-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 186.21 g/mol
Formula C₁₁H₁₀N₂O
badge Registry Numbers
MDL Number MFCD13190645
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to biological targets. Also employed in the preparation of agrochemicals and functional materials. Its structural motif appears in compounds with anti-inflammatory and antimicrobial activities, making it valuable in drug discovery research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,950.00
inventory 250mg
10-20 days ฿5,880.00

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2-Phenoxypyridin-4-amine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to biological targets. Also employed in the preparation of agrochemicals and functional materials. Its structural motif appears in compounds with anti-inflammatory and antimicrobial activities, making it valuabl

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form hydrogen bonds and engage in aromatic interactions, enhancing binding affinity to biological targets. Also employed in the preparation of agrochemicals and functional materials. Its structural motif appears in compounds with anti-inflammatory and antimicrobial activities, making it valuable in drug discovery research.

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