2-(2,3-Dihydro-1H-inden-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
Reagent
Code: #41264
CAS Number
1252793-57-9
blur_circular Chemical Specifications
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Molecular Information
Weight
244.1370 g/mol
Formula
C₁₅H₂₁BO₂
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Registry Numbers
MDL Number
MFCD18383480
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in organic synthesis as a versatile boronic ester reagent. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its stability and reactivity make it a valuable intermediate in the preparation of aryl and heteroaryl compounds. Additionally, it is employed in material science for the development of organic electronic materials, such as polymers and small molecules used in OLEDs and other optoelectronic devices.
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