2-Phenylmalonaldehyde

98%

Reagent Code: #226753
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CAS Number 26591-66-2

science Other reagents with same CAS 26591-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 148.16 g/mol
Formula C₉H₈O₂
badge Registry Numbers
MDL Number MFCD03426041
thermostat Physical Properties
Melting Point 92-95 °C (lit.)
Boiling Point 228.2 °C at 760 mmHg (lit.)
inventory_2 Storage & Handling
Storage −20°C, inert gas

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It participates in condensation reactions to form pyridines, pyrimidines, and other nitrogen-containing rings, which are common structures in pharmaceuticals and agrochemicals. Also employed in the synthesis of fluorescent dyes and optical brighteners due to its ability to form conjugated systems. Its reactive aldehyde groups make it useful in cross-coupling reactions and the development of functional materials.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿9,340.00
5g
10-20 days ฿29,920.00
2-Phenylmalonaldehyde
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Used primarily as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It participates in condensation reactions to form pyridines, pyrimidines, and other nitrogen-containing rings, which are common structures in pharmaceuticals and agrochemicals. Also employed in the synthesis of fluorescent dyes and optical brighteners due to its ability to form conjugated systems. Its reactive aldehyde groups make it useful in cross-coupling reactions and the development of

Used primarily as an intermediate in organic synthesis, particularly in the preparation of heterocyclic compounds. It participates in condensation reactions to form pyridines, pyrimidines, and other nitrogen-containing rings, which are common structures in pharmaceuticals and agrochemicals. Also employed in the synthesis of fluorescent dyes and optical brighteners due to its ability to form conjugated systems. Its reactive aldehyde groups make it useful in cross-coupling reactions and the development of functional materials.

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