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

98%

Reagent Code: #208579
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CAS Number 1073354-66-1

science Other reagents with same CAS 1073354-66-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.11 g/mol
Formula C₁₄H₁₉BO₃
badge Registry Numbers
MDL Number MFCD08669583
thermostat Physical Properties
Boiling Point 358.7±35.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.05±0.1 g/cm3
Storage 2-8℃, sealed, dried

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 aldehyde and boronate functional groups allow dual reactivity, enabling sequential transformations to build aromatic frameworks. Commonly employed in the development of conjugated materials for optoelectronics and in medicinal chemistry to construct biaryl aldehyde derivatives with biological activity. The boronate ester group facilitates mild, selective coupling with aryl halides, making it valuable in late-stage functionalization during drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿2,890.00
250mg
10-20 days ฿4,710.00
1g
10-20 days ฿12,960.00
3-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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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 aldehyde and boronate functional groups allow dual reactivity, enabling sequential transformations to build aromatic frameworks. Commonly employed in the development of conjugated materials for optoelectronics and in medicinal chemistry to construct biaryl aldehyde derivatives with biological activity. The boronate ester group facilitates mild, selective coupling with aryl halides, making it valuable in late-stage functionalization during drug discovery.
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