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

96%

Reagent Code: #166119
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CAS Number 1256360-48-1

science Other reagents with same CAS 1256360-48-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 303.59 g/mol
Formula C₁₆H₁₉BClNO₂
badge Registry Numbers
MDL Number MFCD18087729
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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, while the nitrile and cyclopropyl functionalities provide structural diversity and metabolic stability in drug design. Commonly employed in the development of bioactive compounds and functional materials requiring rigid, three-dimensional architectures.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,630.00
1g
10-20 days ฿10,930.00
5g
10-20 days ฿38,360.00
250mg
10-20 days ฿4,230.00
1-(3-Chloro-5-(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. Its boronate ester group enables efficient carbon-carbon bond formation, while the nitrile and cyclopropyl functionalities provide structural diversity and metabolic stability in drug design. Commonly employed in the development of bioactive compounds and functional materials requiring rigid, three-dimensional architectures.

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, while the nitrile and cyclopropyl functionalities provide structural diversity and metabolic stability in drug design. Commonly employed in the development of bioactive compounds and functional materials requiring rigid, three-dimensional architectures.

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