1-(3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarbonitrile

95%

Reagent Code: #129514
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CAS Number 1818380-84-5

science Other reagents with same CAS 1818380-84-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.17 g/mol
Formula C₁₇H₂₂BNO₂
thermostat Physical Properties
Boiling Point 415.9±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.08±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

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. The boronate ester group enables efficient carbon-carbon bond formation, while the cyclopropane nitrile moiety provides a rigid, polar structural element that can enhance binding affinity in bioactive compounds. Commonly employed in the development of drug candidates where tailored aromatic and strained aliphatic frameworks are required. Its stability and reactivity profile make it suitable for late-stage functionalization in medicinal chemistry campaigns.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,280.00
inventory 250mg
10-20 days ฿16,710.00

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1-(3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)cyclopropanecarbonitrile
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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. The boronate ester group enables efficient carbon-carbon bond formation, while the cyclopropane nitrile moiety provides a rigid, polar structural element that can enhance binding affinity in bioactive compounds. Commonly employed in the development of drug candidates where tailored aromatic and strained aliphatic frameworks are req

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. The boronate ester group enables efficient carbon-carbon bond formation, while the cyclopropane nitrile moiety provides a rigid, polar structural element that can enhance binding affinity in bioactive compounds. Commonly employed in the development of drug candidates where tailored aromatic and strained aliphatic frameworks are required. Its stability and reactivity profile make it suitable for late-stage functionalization in medicinal chemistry campaigns.

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