tert-Butyl (6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)carbamate

97%

Reagent Code: #37087
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CAS Number 1312611-41-8

science Other reagents with same CAS 1312611-41-8

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Weight 369.2623 g/mol
Formula C₂₁H₂₈BNO₄
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MDL Number MFCD13191643
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description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur without interference. Its stability and reactivity make it a versatile intermediate in medicinal chemistry for the development of drug candidates and bioactive compounds.

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inventory 100mg
10-20 days ฿6,012.00

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tert-Butyl (6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)carbamate
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur without interference. Its stability and reactivity make it a ver

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, the tert-butyl carbamate group serves as a protective group for amines, allowing selective reactions to occur without interference. Its stability and reactivity make it a versatile intermediate in medicinal chemistry for the development of drug candidates and bioactive compounds.

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