1-tert-Butyl 2-ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1,2-dicarboxylate

97%

Reagent Code: #39848
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CAS Number 1802005-04-4

science Other reagents with same CAS 1802005-04-4

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Weight 365.2290 g/mol
Formula C₁₈H₂₈BNO₆
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MDL Number MFCD30527899
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This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in cross-coupling reactions. Its boronate ester functional group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl and ethyl ester groups provide stability and reactivity, enabling selective transformations in multi-step synthetic pathways. Its application extends to the development of bioactive compounds and functional materials, where precise control over molecular structure is critical.

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inventory 50mg
10-20 days ฿3,555.00

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1-tert-Butyl 2-ethyl 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrrole-1,2-dicarboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in cross-coupling reactions. Its boronate ester functional group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl and ethyl ester groups provide stability and reactivity, enabling selective

This compound is primarily utilized in organic synthesis as a versatile intermediate, particularly in cross-coupling reactions. Its boronate ester functional group makes it valuable in Suzuki-Miyaura coupling, a widely used method for forming carbon-carbon bonds. This reaction is essential in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Additionally, the tert-butyl and ethyl ester groups provide stability and reactivity, enabling selective transformations in multi-step synthetic pathways. Its application extends to the development of bioactive compounds and functional materials, where precise control over molecular structure is critical.

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