(3-Methoxyphenyl)glyoxal

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Reagent Code: #209821
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CAS Number 32025-65-3

science Other reagents with same CAS 32025-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.16 g/mol
Formula C₉H₈O₃.xH₂O
badge Registry Numbers
MDL Number MFCD05664093
thermostat Physical Properties
Melting Point 99-100 ℃
Boiling Point 95-98 ℃ 0,05mm
inventory_2 Storage & Handling
Density 1.153 g/cm3
Storage Room temperature

description Product Description

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. It participates in cyclization reactions to form heterocyclic compounds, particularly in the development of bioactive molecules such as flavonoids and other aromatic ketone derivatives. Its aldehyde groups enable condensation reactions, making it valuable in the preparation of dyes, fluorescent probes, and functionalized organic frameworks. Also employed in medicinal chemistry research for constructing complex aromatic systems with potential biological activity.

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Test Parameter Specification
Appearance Yellow to pale brown Powder
Purity (%) 96.5-100
Water 0-22%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,520.00
inventory 1g
10-20 days ฿9,960.00

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(3-Methoxyphenyl)glyoxal
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Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. It participates in cyclization reactions to form heterocyclic compounds, particularly in the development of bioactive molecules such as flavonoids and other aromatic ketone derivatives. Its aldehyde groups enable condensation reactions, making it valuable in the preparation of dyes, fluorescent probes, and functionalized organic frameworks. Also employed in medicinal chemistry research for constructing complex aromatic s

Used in organic synthesis as an intermediate for pharmaceuticals and fine chemicals. It participates in cyclization reactions to form heterocyclic compounds, particularly in the development of bioactive molecules such as flavonoids and other aromatic ketone derivatives. Its aldehyde groups enable condensation reactions, making it valuable in the preparation of dyes, fluorescent probes, and functionalized organic frameworks. Also employed in medicinal chemistry research for constructing complex aromatic systems with potential biological activity.

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