2-(4-(3,4-Difluorophenyl)thiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
95%
Reagent
Code: #89625
CAS Number
1402227-89-7
science Other reagents with same CAS 1402227-89-7
blur_circular Chemical Specifications
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Molecular Information
Weight
322.18 g/mol
Formula
C₁₆H₁₇BF₂O₂S
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Registry Numbers
MDL Number
MFCD18436139
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Storage & Handling
Storage
-20°C, sealed, dry
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds between aryl or heteroaryl groups. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructing complex organic molecules. Additionally, it is used in the development of organic electronic materials, including OLEDs and semiconductors, due to its ability to facilitate precise molecular design.
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