2-Amino-4-pyridinylmethanol

97%

Reagent Code: #135392
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CAS Number 105250-17-7

science Other reagents with same CAS 105250-17-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 124.14 g/mol
Formula C₆H₈N₂O
badge Registry Numbers
MDL Number MFCD03791261
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocyclic compounds, which are common in drugs targeting cancer and inflammatory diseases. Also employed in research for developing novel antimicrobial agents due to its ability to interact with bacterial enzyme systems. The hydroxyl and amino groups allow for easy functionalization, making it valuable in combinatorial chemistry and drug discovery.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 5g
10-20 days ฿804.00
inventory 25g
10-20 days ฿6,590.00
inventory 100g
10-20 days ฿26,360.00
2-Amino-4-pyridinylmethanol
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocyclic compounds, which are common in drugs targeting cancer and inflammatory diseases. Also employed in research for developing novel antimicrobial agents due to its ability to interact with bacterial enzyme systems. The hydroxyl and amino groups allow for easy functionalization, making it valuab

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of nitrogen-containing heterocyclic compounds, which are common in drugs targeting cancer and inflammatory diseases. Also employed in research for developing novel antimicrobial agents due to its ability to interact with bacterial enzyme systems. The hydroxyl and amino groups allow for easy functionalization, making it valuable in combinatorial chemistry and drug discovery.

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