Dimethyl-[4-(4,4,5,5-Tetramethyl[1,3,2]Dioxaborolan-2-Yl)Benzyl]Amine

98%

Reagent Code: #179224
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CAS Number 878197-87-6

science Other reagents with same CAS 878197-87-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.17 g/mol
Formula C₁₅H₂₄BNO₂
badge Registry Numbers
MDL Number MFCD04971190
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, while the dimethylamine benzyl moiety provides opportunities for further functionalization and tuning of chemical and biological properties. This versatility makes it valuable in drug discovery, lead compound optimization, development of functional materials, and preparation of bioactive compounds and conjugated systems for electronic applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,610.00
inventory 1g
10-20 days ฿4,200.00
inventory 5g
10-20 days ฿18,320.00

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Dimethyl-[4-(4,4,5,5-Tetramethyl[1,3,2]Dioxaborolan-2-Yl)Benzyl]Amine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, while the dimethylamine benzyl moiety provides opportunities for further functionalization and tuning of chemical and biological properties. This versatility makes it valuable in drug discovery, lead compound optimization, development o

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical industries. Its boronate ester group facilitates carbon-carbon bond formation under mild conditions, while the dimethylamine benzyl moiety provides opportunities for further functionalization and tuning of chemical and biological properties. This versatility makes it valuable in drug discovery, lead compound optimization, development of functional materials, and preparation of bioactive compounds and conjugated systems for electronic applications.

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