(2-Bromo-5-methylthiazol-4-yl)methanol

95%

Reagent Code: #36408
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CAS Number 1187836-86-7

science Other reagents with same CAS 1187836-86-7

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Weight 208.0762 g/mol
Formula C₅H₆BrNOS
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(2-Bromo-5-methylthiazol-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 targeting therapeutic applications. The bromo and hydroxymethyl functional groups on the thiazole ring make it a versatile building block for constructing complex molecules, such as potential drug candidates for treating infections, inflammation, or other diseases. Additionally, its thiazole core is often explored in the design of agrochemicals, including pesticides and herbicides, due to its structural relevance in bioactive molecules. Researchers also leverage its reactivity in coupling reactions and further functionalization to create novel chemical entities for material science applications.

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inventory 50mg
10-20 days ฿7,020.00

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(2-Bromo-5-methylthiazol-4-yl)methanol
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(2-Bromo-5-methylthiazol-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 targeting therapeutic applications. The bromo and hydroxymethyl functional groups on the thiazole ring make it a versatile building block for constructing complex molecules, such as potential drug candidates for treating infections, inflammation, or other diseases. Additionally, its th

(2-Bromo-5-methylthiazol-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 targeting therapeutic applications. The bromo and hydroxymethyl functional groups on the thiazole ring make it a versatile building block for constructing complex molecules, such as potential drug candidates for treating infections, inflammation, or other diseases. Additionally, its thiazole core is often explored in the design of agrochemicals, including pesticides and herbicides, due to its structural relevance in bioactive molecules. Researchers also leverage its reactivity in coupling reactions and further functionalization to create novel chemical entities for material science applications.

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