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

99%

Product Code: 242156

CAS: 1187525-03-6

Molecular Weight:	Molecular Formula:	C₁₅H₂₁BO₂
EC Number:	MDL Number:
Melting Point:	Boiling Point:
Density:	Storage Condition:	2-8℃

Product Description: Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its structure stabilizes the boronate functionality, making it suitable for palladium-catalyzed coupling with aryl or vinyl halides to construct substituted olefins and biaryl systems. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials where precise molecular architecture is required. The compound's steric bulk and electron-donating groups enhance reaction selectivity and yield under mild conditions.

Sizes / Availability / Pricing:

Size	Availability	Price	Quantity
0.100	10-20 days	Ft47,048.22	+ -
0.500	10-20 days	Ft137,589.91	+ -
1.000	10-20 days	Ft221,440.29	+ -

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

Used as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in organic synthesis. Its structure stabilizes the boronate functionality, making it suitable for palladium-catalyzed coupling with aryl or vinyl halides to construct substituted olefins and biaryl systems. Commonly employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials where precise molecular architecture is required. The compound's steric bulk and electron-donating groups enhance reaction selectivity and yield under mild conditions.

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

99%

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