3-(4-(Tributylstannyl)thiazol-2-yl)oxetan-3-ol

Reagent Code: #242414
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CAS Number 1245816-13-0

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Weight 446.24 g/mol
Formula C₁₈H₃₃NO₂SSn
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MDL Number MFCD16140389
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Storage Room temperature

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Used primarily as an intermediate in organic synthesis, especially in cross-coupling reactions such as Stille coupling, to construct complex organic molecules. Its stannyl group facilitates carbon-carbon bond formation by enabling the transfer of the thiazolyl moiety to coupling partners, making it valuable in pharmaceutical and agrochemical research for building heterocyclic frameworks. The oxetane moiety contributes to metabolic stability and solubility, which is beneficial in drug design. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required.

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inventory 1g
10-20 days ฿119,640.00

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3-(4-(Tributylstannyl)thiazol-2-yl)oxetan-3-ol
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Used primarily as an intermediate in organic synthesis, especially in cross-coupling reactions such as Stille coupling, to construct complex organic molecules. Its stannyl group facilitates carbon-carbon bond formation by enabling the transfer of the thiazolyl moiety to coupling partners, making it valuable in pharmaceutical and agrochemical research for building heterocyclic frameworks. The oxetane moiety contributes to metabolic stability and solubility, which is beneficial in drug design. Commonly emp

Used primarily as an intermediate in organic synthesis, especially in cross-coupling reactions such as Stille coupling, to construct complex organic molecules. Its stannyl group facilitates carbon-carbon bond formation by enabling the transfer of the thiazolyl moiety to coupling partners, making it valuable in pharmaceutical and agrochemical research for building heterocyclic frameworks. The oxetane moiety contributes to metabolic stability and solubility, which is beneficial in drug design. Commonly employed in the development of bioactive compounds and functional materials where precise molecular architecture is required.

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