(1-Phenyl-1H-benzo[d]imidazol-5-yl)boronic acid
98%
Reagent
Code: #227532
CAS Number
1803179-52-3
science Other reagents with same CAS 1803179-52-3
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Molecular Information
Weight
238.05 g/mol
Formula
C₁₃H₁₁BN₂O₂
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Registry Numbers
MDL Number
MFCD27935833
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Storage & Handling
Storage
2-8°C, Inert Gas
description Product Description
Used in organic synthesis as a key building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of biaryl compounds which are important in pharmaceutical and agrochemical development. Its boronic acid group facilitates carbon-carbon bond formation under mild conditions, making it valuable in drug discovery for constructing complex aromatic structures. Commonly employed in the synthesis of bioactive molecules, particularly those targeting central nervous system disorders and inflammatory diseases due to the presence of the benzimidazole core, known for its pharmacological relevance. Also utilized in materials science for designing fluorescent probes and organic electronic materials.
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