(E)-2-(Benzyloxy)-1-methoxy-4-(2-nitrovinyl)benzene

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Reagent Code: #181136
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CAS Number 63909-29-5

science Other reagents with same CAS 63909-29-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.29 g/mol
Formula C₁₆H₁₅NO₄
thermostat Physical Properties
Melting Point 128-131 °C(lit.)
inventory_2 Storage & Handling
Density 1.212 g/cm3
Storage 2-8°C, sealed, dry

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its nitrovinyl group allows participation in Michael addition reactions, making it valuable in constructing carbon-carbon bonds. Commonly employed in the development of bioactive molecules, including potential antitumor and antimicrobial agents. Also utilized in the preparation of fluorescent dyes and optoelectronic materials due to its conjugated structure. Stable under standard conditions and compatible with various functional group transformations, it supports multi-step synthetic routes in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,210.00
inventory 5g
10-20 days ฿7,700.00
inventory 25g
10-20 days ฿29,180.00

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(E)-2-(Benzyloxy)-1-methoxy-4-(2-nitrovinyl)benzene
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its nitrovinyl group allows participation in Michael addition reactions, making it valuable in constructing carbon-carbon bonds. Commonly employed in the development of bioactive molecules, including potential antitumor and antimicrobial agents. Also utilized in the preparation of fluorescent dyes and optoelectronic materials due to its conjugated structure. Stable under standard conditions and compatible with various fu

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. Its nitrovinyl group allows participation in Michael addition reactions, making it valuable in constructing carbon-carbon bonds. Commonly employed in the development of bioactive molecules, including potential antitumor and antimicrobial agents. Also utilized in the preparation of fluorescent dyes and optoelectronic materials due to its conjugated structure. Stable under standard conditions and compatible with various functional group transformations, it supports multi-step synthetic routes in medicinal chemistry.

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