(2-Phenylthiazol-5-yl)methanol

95%

Reagent Code: #227645
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CAS Number 859485-91-9

science Other reagents with same CAS 859485-91-9

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Weight 191.25 g/mol
Formula C₁₀H₉NOS
badge Registry Numbers
MDL Number MFCD09694149
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block for thiazole-based drugs due to its ability to enhance metabolic stability and binding affinity. Commonly employed in the development of anticonvulsant and anti-inflammatory agents. Also utilized in agrochemicals for designing novel pesticides with improved efficacy. Its hydroxyl group allows for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,290.00
inventory 250mg
10-20 days ฿5,350.00
inventory 1g
10-20 days ฿20,370.00

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(2-Phenylthiazol-5-yl)methanol
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block for thiazole-based drugs due to its ability to enhance metabolic stability and binding affinity. Commonly employed in the development of anticonvulsant and anti-inflammatory agents. Also utilized in agrochemicals for designing novel pesticides with improved efficacy. Its hydroxyl group allows for easy functionalization, making
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders. It serves as a building block for thiazole-based drugs due to its ability to enhance metabolic stability and binding affinity. Commonly employed in the development of anticonvulsant and anti-inflammatory agents. Also utilized in agrochemicals for designing novel pesticides with improved efficacy. Its hydroxyl group allows for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.
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