2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

98%

Reagent Code: #208580
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CAS Number 269410-05-1

science Other reagents with same CAS 269410-05-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.15784 g/mol
Formula C₁₇H₂₁BO₃
badge Registry Numbers
MDL Number MFCD22414442
thermostat Physical Properties
Boiling Point 419.5±28.0℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.08±0.1 g/cm3
Storage 2-8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in pharmaceutical and agrochemical industries for constructing naphthalene-based structures with high efficiency and selectivity. Its boronate ester group facilitates mild and catalytic coupling conditions, making it ideal for late-stage functionalization in drug development. Also applied in materials science for designing organic semiconductors and fluorescent dyes due to the extended aromatic system.

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inventory 1g
10-20 days ฿5,900.00

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2-(2-methoxy-1-naphthalenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in pharmaceutical and agrochemical industries for constructing naphthalene-based structures with high efficiency and selectivity. Its boronate ester group facilitates mild and catalytic coupling conditions, making it ideal for late-stage functionalization in drug development. Also applied in materials science for designin

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in pharmaceutical and agrochemical industries for constructing naphthalene-based structures with high efficiency and selectivity. Its boronate ester group facilitates mild and catalytic coupling conditions, making it ideal for late-stage functionalization in drug development. Also applied in materials science for designing organic semiconductors and fluorescent dyes due to the extended aromatic system.

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