4-(Pyridin-2-yl)phenol

95%

Reagent Code: #225479
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CAS Number 51035-40-6

science Other reagents with same CAS 51035-40-6

blur_circular Chemical Specifications

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Weight 171.2 g/mol
Formula C₁₁H₉NO
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MDL Number MFCD00464189
inventory_2 Storage & Handling
Storage Room temperature

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 the preparation of ligands for metal-catalyzed reactions, especially in palladium-catalyzed cross-coupling processes. Also employed in the design of functional materials, including sensors and optoelectronic devices, due to its ability to coordinate with metals and participate in electron-transfer processes. Its structural motif appears in compounds studied for antimicrobial and anti-inflammatory activities.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,050.00
inventory 10g
10-20 days ฿2,070.00
inventory 25g
10-20 days ฿5,160.00
inventory 100g
10-20 days ฿20,610.00

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4-(Pyridin-2-yl)phenol
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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 the preparation of ligands for metal-catalyzed reactions, especially in palladium-catalyzed cross-coupling processes. Also employed in the design of functional materials, including sensors and optoelectronic devices, due to its ability to coordinate with metals and participate in electron-transfer processes. Its structural motif appear

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 the preparation of ligands for metal-catalyzed reactions, especially in palladium-catalyzed cross-coupling processes. Also employed in the design of functional materials, including sensors and optoelectronic devices, due to its ability to coordinate with metals and participate in electron-transfer processes. Its structural motif appears in compounds studied for antimicrobial and anti-inflammatory activities.

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