Trans-4-Methoxy-β-Nitrostyrene

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Reagent Code: #241039
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CAS Number 5576-97-6

science Other reagents with same CAS 5576-97-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.17 g/mol
Formula C₉H₉NO₃
badge Registry Numbers
MDL Number MFCD00024826
thermostat Physical Properties
Melting Point 86-88 °C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the synthesis of various bioactive molecules due to its conjugated nitroalkene structure, which readily undergoes Michael addition and cyclization reactions. Commonly employed in the development of analgesic, anti-inflammatory, and antimicrobial agents. Also utilized in the synthesis of dyes and fluorescent compounds owing to its aromatic and electron-withdrawing functional groups. Its trans configuration enhances stability and reactivity in stereoselective transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿550.00
inventory 5g
10-20 days ฿1,630.00
inventory 25g
10-20 days ฿6,900.00
inventory 100g
10-20 days ฿26,900.00

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Trans-4-Methoxy-β-Nitrostyrene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the synthesis of various bioactive molecules due to its conjugated nitroalkene structure, which readily undergoes Michael addition and cyclization reactions. Commonly employed in the development of analgesic, anti-inflammatory, and antimicrobial agents. Also utilized in the synthesis of dyes and fluorescent compounds owing to its aromatic and electron-withd

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and fine chemicals. It serves as a building block in the synthesis of various bioactive molecules due to its conjugated nitroalkene structure, which readily undergoes Michael addition and cyclization reactions. Commonly employed in the development of analgesic, anti-inflammatory, and antimicrobial agents. Also utilized in the synthesis of dyes and fluorescent compounds owing to its aromatic and electron-withdrawing functional groups. Its trans configuration enhances stability and reactivity in stereoselective transformations.

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