trans-2-Methyl-2-butenal

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Reagent Code: #207660
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CAS Number 497-03-0

science Other reagents with same CAS 497-03-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 84.12 g/mol
Formula C₅H₈O
badge Registry Numbers
MDL Number MFCD00006977
thermostat Physical Properties
Boiling Point 116°C
inventory_2 Storage & Handling
Density 0.87g/mL
Storage Room temperature, dryness, inert gas storage

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the production of fragrances and flavorings due to its aldehyde functionality and conjugated structure. It serves as a building block in the synthesis of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its α,β-unsaturated aldehyde structure makes it suitable for Michael addition and other nucleophilic reactions, enabling the formation of carbon-carbon bonds. Additionally, it finds use in research settings for developing novel synthetic pathways and studying reaction mechanisms involving unsaturated carbonyl systems.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mL
10-20 days ฿3,040.00
inventory 25ml
10-20 days ฿11,000.00
inventory 100ml
10-20 days ฿29,990.00

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trans-2-Methyl-2-butenal
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the production of fragrances and flavorings due to its aldehyde functionality and conjugated structure. It serves as a building block in the synthesis of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its α,β-unsaturated aldehyde structure makes it suitable for Michael addition and other nucleophilic reactions, enabling the formation of carbon-carbon bonds. Additionally, it f

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the production of fragrances and flavorings due to its aldehyde functionality and conjugated structure. It serves as a building block in the synthesis of more complex molecules, particularly in the pharmaceutical and agrochemical industries. Its α,β-unsaturated aldehyde structure makes it suitable for Michael addition and other nucleophilic reactions, enabling the formation of carbon-carbon bonds. Additionally, it finds use in research settings for developing novel synthetic pathways and studying reaction mechanisms involving unsaturated carbonyl systems.

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