2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate

Reagent Code: #77082
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CAS Number 1242156-76-8

science Other reagents with same CAS 1242156-76-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 494.36 g/mol
Formula C₂₇H₃₂BFN₂O₅
badge Registry Numbers
MDL Number MFCD26403976
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in complex molecules. The presence of the phthalazine moiety enhances its potential as a building block for biologically active compounds, including inhibitors and modulators of specific enzymes or receptors. Additionally, the tert-butyl and fluorine substituents contribute to its stability and selectivity in various chemical transformations, making it a versatile reagent in medicinal chemistry research. Its application extends to the synthesis of novel drug candidates targeting diseases such as cancer, inflammation, and infectious diseases.

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inventory 1g
10-20 days ฿545,904.00

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2-(6-(tert-butyl)-8-fluoro-1-oxophthalazin-2(1H)-yl)-6-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)benzyl acetate
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This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in complex molecules. The presence of the phthalazine moiety enhances its potential as a building block for biologically active compounds, including inhibitors and modulators of specific enzymes or

This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it a valuable intermediate in Suzuki-Miyaura cross-coupling reactions, which are widely employed to construct carbon-carbon bonds in complex molecules. The presence of the phthalazine moiety enhances its potential as a building block for biologically active compounds, including inhibitors and modulators of specific enzymes or receptors. Additionally, the tert-butyl and fluorine substituents contribute to its stability and selectivity in various chemical transformations, making it a versatile reagent in medicinal chemistry research. Its application extends to the synthesis of novel drug candidates targeting diseases such as cancer, inflammation, and infectious diseases.

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