
Catalog Number	AR01DJKR
Chemical Name	2-(3-methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number	627526-33-4
Molecular Formula	C17H21BO3
Molecular Weight	284.1578
MDL Number	MFCD22494802
SMILES	COc1cc(B2OC(C(O2)(C)C)(C)C)c2c(c1)cccc2

2-(3-Methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, commonly known as $name$, is a versatile compound widely utilized in chemical synthesis. This boron-containing compound plays a crucial role in various organic reactions due to its unique structure and reactivity.One key application of $name$ is as a boronic ester in Suzuki-Miyaura cross-coupling reactions. In this process, $name$ serves as a boron source, enabling the formation of carbon-carbon bonds under mild reaction conditions. This reaction is highly valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and materials.Additionally, $name$ can participate in transition metal-catalyzed transformations, such as palladium-catalyzed C-C bond formation reactions. By coupling with different organic substrates, $name$ facilitates the construction of biaryl compounds, which are prevalent in medicinal chemistry and material science.Furthermore, the presence of the methoxy and tetramethyl groups in $name$ enhances its stability and solubility, making it a practical choice for chemical reactions. Overall, the unique properties of 2-(3-Methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane make it a valuable tool in organic synthesis, enabling the efficient construction of diverse organic molecules with high selectivity and efficiency.

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Packsize	Purity	Price	Availability
50mg	95%	$39.00	Global Stock	Buy Now	Add To Cart
100mg	95%	$52.00	Global Stock	Buy Now	Add To Cart
250mg	95%	$94.00	Global Stock	Buy Now	Add To Cart
1g	95%	$257.00	Global Stock	Buy Now	Add To Cart

2-(3-methoxynaphthalen-1-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane