(2,5-Dimethyloxazol-4-yl)methanol

95%

Reagent Code: #36305
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CAS Number 92901-94-5

science Other reagents with same CAS 92901-94-5

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Weight 127.1412 g/mol
Formula C₆H₉NO₂
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MDL Number MFCD07772804
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(2,5-Dimethyloxazol-4-yl)methanol is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of heterocyclic molecules. Its oxazole ring structure is valuable in medicinal chemistry for designing drugs with potential antimicrobial, anti-inflammatory, or anticancer properties. Additionally, it is used in the preparation of ligands for catalysis and in the study of chemical reactions involving nitrogen-containing heterocycles. Its applications also extend to material science, where it contributes to the development of functionalized polymers and advanced organic materials.

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inventory 100mg
10-20 days ฿2,232.00

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(2,5-Dimethyloxazol-4-yl)methanol
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(2,5-Dimethyloxazol-4-yl)methanol is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of heterocyclic molecules. Its oxazole ring structure is valuable in medicinal chemistry for designing drugs with potential antimicrobial, anti-inflammatory, or anticancer properties. Additionally, it is used in the preparation of ligands for catalysis and in the study of chemical reaction

(2,5-Dimethyloxazol-4-yl)methanol is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of various bioactive compounds, particularly in the synthesis of heterocyclic molecules. Its oxazole ring structure is valuable in medicinal chemistry for designing drugs with potential antimicrobial, anti-inflammatory, or anticancer properties. Additionally, it is used in the preparation of ligands for catalysis and in the study of chemical reactions involving nitrogen-containing heterocycles. Its applications also extend to material science, where it contributes to the development of functionalized polymers and advanced organic materials.

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