6-Isopropoxynaphthalene-2-boronic acid

98%

Reagent Code: #130370
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CAS Number 1334221-34-9

science Other reagents with same CAS 1334221-34-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.07 g/mol
Formula C₁₃H₁₅BO₃
badge Registry Numbers
MDL Number MFCD16260719
thermostat Physical Properties
Boiling Point 424.2±37.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of liquid crystals, fluorescent dyes, and conjugated materials for optoelectronics. Also utilized in medicinal chemistry for constructing naphthalene-based drug candidates with anti-inflammatory or anticancer activity. The isopropoxy group enhances solubility and influences electronic properties, improving reaction selectivity and final compound performance.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,310.00
inventory 250mg
10-20 days ฿3,720.00

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6-Isopropoxynaphthalene-2-boronic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of liquid crystals, fluorescent dyes, and conjugated materials for optoelectronics. Also utilized in medicinal chemistry for constructing naphthalene-based drug candidates with anti-inflammatory or anticancer act

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form biaryl compounds. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly employed in the development of liquid crystals, fluorescent dyes, and conjugated materials for optoelectronics. Also utilized in medicinal chemistry for constructing naphthalene-based drug candidates with anti-inflammatory or anticancer activity. The isopropoxy group enhances solubility and influences electronic properties, improving reaction selectivity and final compound performance.

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