2,3-Difluoro-6-(methoxymethoxy)benzaldehyde

98%

Reagent Code: #179648
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CAS Number 1075701-01-7

science Other reagents with same CAS 1075701-01-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.15 g/mol
Formula C₉H₈F₂O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated organic molecules with enhanced metabolic stability and bioavailability. Its aldehyde functionality allows for versatile chemical transformations, such as condensation and reduction reactions, enabling the construction of complex molecular architectures. The presence of fluorine atoms and a protected hydroxyl group (via methoxymethoxy) makes it valuable in medicinal chemistry for tuning electronic and steric properties, improving drug-target interactions. Commonly employed in the preparation of bioactive molecules, including potential antiviral and anticancer agents.

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inventory 100mg
10-20 days ฿4,280.00

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2,3-Difluoro-6-(methoxymethoxy)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated organic molecules with enhanced metabolic stability and bioavailability. Its aldehyde functionality allows for versatile chemical transformations, such as condensation and reduction reactions, enabling the construction of complex molecular architectures. The presence of fluorine atoms and a protected hydroxyl group (via methoxymethoxy) makes it valuable in medicinal chemistry for tuning

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of fluorinated organic molecules with enhanced metabolic stability and bioavailability. Its aldehyde functionality allows for versatile chemical transformations, such as condensation and reduction reactions, enabling the construction of complex molecular architectures. The presence of fluorine atoms and a protected hydroxyl group (via methoxymethoxy) makes it valuable in medicinal chemistry for tuning electronic and steric properties, improving drug-target interactions. Commonly employed in the preparation of bioactive molecules, including potential antiviral and anticancer agents.

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