(2-Phenylthiazol-4-yl)methanol

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Reagent Code: #36454
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CAS Number 23780-13-4

science Other reagents with same CAS 23780-13-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.2500 g/mol
Formula C₁₀H₉NOS
badge Registry Numbers
MDL Number MFCD02682017
thermostat Physical Properties
Melting Point 67 °C
Boiling Point 372.2 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.264g/cm3
Storage 2-8°C

description Product Description

(2-Phenylthiazol-4-yl)methanol is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those with potential therapeutic applications. The compound's structure, featuring a phenylthiazole moiety, makes it valuable in the design of molecules targeting specific enzymes or receptors. It is often employed in the synthesis of heterocyclic compounds, which are widely explored for their antimicrobial, anti-inflammatory, and anticancer properties. Additionally, its functional groups allow for further chemical modifications, enabling researchers to create diverse derivatives for drug discovery and optimization.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿864.00
inventory 1g
10-20 days ฿2,500.00
inventory 5g
10-20 days ฿12,450.00
inventory 25g
10-20 days ฿54,080.00
inventory 10g
10-20 days ฿24,880.00

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(2-Phenylthiazol-4-yl)methanol
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(2-Phenylthiazol-4-yl)methanol is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various biologically active compounds, particularly those with potential therapeutic applications. The compound's structure, featuring a phenylthiazole moiety, makes it valuable in the design of molecules targeting specific enzymes or receptors. It is often employed in the synthesis of heterocyclic compounds, which are widely explored for their antimicrobial, anti-inflammatory, and anticancer properties. Additionally, its functional groups allow for further chemical modifications, enabling researchers to create diverse derivatives for drug discovery and optimization.
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