Methyl Phenylpropiolate

98%

Reagent Code: #206327
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CAS Number 4891-38-7

science Other reagents with same CAS 4891-38-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 160.17 g/mol
Formula C₁₀H₈O₂
badge Registry Numbers
MDL Number MFCD00041685
thermostat Physical Properties
Boiling Point 109-112°C 2mm Hg (Lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used primarily as a building block in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. It serves as a reactive ester in conjugation with alkynes and alkenes through cycloaddition reactions, making it valuable in the development of complex molecular structures. Commonly employed in research settings for synthesizing chalcone derivatives and other biologically active compounds. Its α,β-unsaturated carbonyl system allows for Michael addition reactions, useful in creating carbon-carbon bonds. Also utilized in the design of photoactive compounds and fluorescent probes due to its conjugated structure.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿430.00
inventory 5g
10-20 days ฿1,570.00
inventory 25g
10-20 days ฿6,560.00
Methyl Phenylpropiolate
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Used primarily as a building block in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. It serves as a reactive ester in conjugation with alkynes and alkenes through cycloaddition reactions, making it valuable in the development of complex molecular structures. Commonly employed in research settings for synthesizing chalcone derivatives and other biologically active compounds. Its α,β-unsaturated carbonyl system allows for Michael addition reactions, useful in creati

Used primarily as a building block in organic synthesis, especially in the preparation of pharmaceuticals and fine chemicals. It serves as a reactive ester in conjugation with alkynes and alkenes through cycloaddition reactions, making it valuable in the development of complex molecular structures. Commonly employed in research settings for synthesizing chalcone derivatives and other biologically active compounds. Its α,β-unsaturated carbonyl system allows for Michael addition reactions, useful in creating carbon-carbon bonds. Also utilized in the design of photoactive compounds and fluorescent probes due to its conjugated structure.

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