5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzo[d]thiazole
97%
Reagent
Code: #241639
CAS Number
1073354-91-2
blur_circular Chemical Specifications
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Molecular Information
Weight
261.15 g/mol
Formula
C₁₃H₁₆BNO₂S
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Registry Numbers
MDL Number
MFCD09260439
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Physical Properties
Boiling Point
380.6±15.0°C at 760 mmHg
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Storage & Handling
Storage
2-8°C, stored in inert gas
description Product Description
Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and organic electronic materials. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing the formation of biaryl and heteroaryl structures found in bioactive molecules. It is particularly valuable in drug discovery for constructing complex thiazole-containing scaffolds. Additionally, it finds use in materials science for developing fluorescent dyes and organic semiconductors due to the electron-accepting nature of the benzo[d]thiazole core.
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