(2-(Pyridin-4-yl)thiazol-5-yl)methanol

Reagent Code: #226900
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CAS Number 1267675-85-3

science Other reagents with same CAS 1267675-85-3

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scatter_plot Molecular Information
Weight 192.24 g/mol
Formula C₉H₈N₂OS
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. Commonly employed in the preparation of antitumor and anti-inflammatory agents due to its ability to interact with biological targets through hydrogen bonding and π-π stacking interactions. Also utilized in the design of new drug candidates targeting neurological disorders owing to its blood-brain barrier permeability potential.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,200.00
(2-(Pyridin-4-yl)thiazol-5-yl)methanol
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. Commonly employed in the preparation of antitumor and anti-inflammatory agents due to its ability to interact with biological targets through hydrogen bonding and π-π stacking interactions. Also utilized in the des

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for creating analogs with enhanced biological activity. Commonly employed in the preparation of antitumor and anti-inflammatory agents due to its ability to interact with biological targets through hydrogen bonding and π-π stacking interactions. Also utilized in the design of new drug candidates targeting neurological disorders owing to its blood-brain barrier permeability potential.

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