4-(Aminomethyl)pyridin-3-ol

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Reagent Code: #137765
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CAS Number 20485-35-2

science Other reagents with same CAS 20485-35-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 124.14 g/mol
Formula C₆H₈N₂O
badge Registry Numbers
MDL Number MFCD11100730
inventory_2 Storage & Handling
Storage 2-8°C, storage away from light, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide adenine dinucleotide (NAD)-related compounds and enzyme inhibitors. Its structure supports the creation of bioactive molecules with potential applications in treating metabolic and neurodegenerative disorders. Also employed in the preparation of ligands for catalytic processes and in the design of sensors due to its ability to coordinate with metal ions. Its amine and hydroxyl functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry and organic synthesis.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿26,520.00

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4-(Aminomethyl)pyridin-3-ol
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide adenine dinucleotide (NAD)-related compounds and enzyme inhibitors. Its structure supports the creation of bioactive molecules with potential applications in treating metabolic and neurodegenerative disorders. Also employed in the preparation of ligands for catalytic processes and in the design of sensors due to its ability to coordinate with metal ions. Its amine and hydroxyl functional groups al
Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinamide adenine dinucleotide (NAD)-related compounds and enzyme inhibitors. Its structure supports the creation of bioactive molecules with potential applications in treating metabolic and neurodegenerative disorders. Also employed in the preparation of ligands for catalytic processes and in the design of sensors due to its ability to coordinate with metal ions. Its amine and hydroxyl functional groups allow for versatile chemical modifications, making it valuable in medicinal chemistry and organic synthesis.
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