(1-Phenyl-1H-benzo[d]imidazol-5-yl)boronic acid

98%

Reagent Code: #227532
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CAS Number 1803179-52-3

science Other reagents with same CAS 1803179-52-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.05 g/mol
Formula C₁₃H₁₁BN₂O₂
badge Registry Numbers
MDL Number MFCD27935833
inventory_2 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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,000.00
250mg
10-20 days ฿13,800.00
1g
10-20 days ฿30,190.00
(1-Phenyl-1H-benzo[d]imidazol-5-yl)boronic acid
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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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