2-Nitrocinnamaldehyde, predominantly trans

98%

Reagent Code: #217378
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CAS Number 1466-88-2

science Other reagents with same CAS 1466-88-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.16 g/mol
Formula C₉H₇NO₃
badge Registry Numbers
MDL Number MFCD00007188
thermostat Physical Properties
Melting Point 125-126°C
Boiling Point 348.1°C
inventory_2 Storage & Handling
Density 1.269g/cm3
Storage Room temperature, inert gas environment

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Acts as a building block in the preparation of nitro-containing compounds due to its conjugated system and reactive aldehyde group. Employed in photochemical studies because of its light-sensitive properties, particularly in the development of photo-switchable molecules. Also utilized in the synthesis of heterocyclic compounds, including indoles and quinolines, through cyclization reactions. Its trans configuration enhances stability and reactivity in condensation and addition reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿770.00
inventory 5g
10-20 days ฿2,710.00

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2-Nitrocinnamaldehyde, predominantly trans
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Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Acts as a building block in the preparation of nitro-containing compounds due to its conjugated system and reactive aldehyde group. Employed in photochemical studies because of its light-sensitive properties, particularly in the development of photo-switchable molecules. Also utilized in the synthesis of heterocyclic compounds, including indoles and quinolines, through cyclization reactions. Its trans configuration enhanc

Used in organic synthesis as an intermediate for pharmaceuticals and agrochemicals. Acts as a building block in the preparation of nitro-containing compounds due to its conjugated system and reactive aldehyde group. Employed in photochemical studies because of its light-sensitive properties, particularly in the development of photo-switchable molecules. Also utilized in the synthesis of heterocyclic compounds, including indoles and quinolines, through cyclization reactions. Its trans configuration enhances stability and reactivity in condensation and addition reactions.

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