3-Nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile

98%

Reagent Code: #219652
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CAS Number 1392812-18-8

science Other reagents with same CAS 1392812-18-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.08 g/mol
Formula C₁₃H₁₅BN₂O₄
badge Registry Numbers
MDL Number MFCD22571939
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive compounds and functional materials. The nitrile and nitro groups allow further chemical modifications, enhancing its utility in multi-step syntheses. Commonly employed in the preparation of nitrogen-containing aromatic compounds and conjugated systems for use in medicinal chemistry and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,470.00
inventory 250mg
10-20 days ฿2,380.00
inventory 1g
10-20 days ฿6,690.00
inventory 5g
10-20 days ฿27,300.00
3-Nitro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzonitrile
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive compounds and functional materials. The nitrile and nitro groups allow further chemical modifications, enhancing its utility in multi-step syntheses. Commonly employed in the preparation of nitrogen-containing

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronate ester group enables efficient carbon-carbon bond formation, making it valuable in the development of bioactive compounds and functional materials. The nitrile and nitro groups allow further chemical modifications, enhancing its utility in multi-step syntheses. Commonly employed in the preparation of nitrogen-containing aromatic compounds and conjugated systems for use in medicinal chemistry and materials science.

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