Pent-4-ynal

98%

Reagent Code: #226725
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CAS Number 18498-59-4

science Other reagents with same CAS 18498-59-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 82.10 g/mol
Formula C₆H₆O
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Pent-4-ynal is primarily used as a building block in organic synthesis, particularly in the development of complex molecules in pharmaceutical and agrochemical research. Its aldehyde and terminal alkyne functional groups allow it to participate in a variety of transformations, including Wittig reactions, nucleophilic additions, and metal-catalyzed couplings such as Sonogashira and click chemistry. This dual reactivity makes it valuable for constructing carbon-carbon bonds and introducing functionalized side chains. It is also employed in the synthesis of natural products and bioactive compounds where a five-carbon chain with both unsaturation and reactivity is required. Its versatility in multistep syntheses enhances its utility in medicinal chemistry and materials science.

Available Sizes & Pricing

Size Availability Unit Price Quantity
10mg
10-20 days ฿700.00
50mg
10-20 days ฿2,360.00
Pent-4-ynal
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Pent-4-ynal is primarily used as a building block in organic synthesis, particularly in the development of complex molecules in pharmaceutical and agrochemical research. Its aldehyde and terminal alkyne functional groups allow it to participate in a variety of transformations, including Wittig reactions, nucleophilic additions, and metal-catalyzed couplings such as Sonogashira and click chemistry. This dual reactivity makes it valuable for constructing carbon-carbon bonds and introducing functionalized s

Pent-4-ynal is primarily used as a building block in organic synthesis, particularly in the development of complex molecules in pharmaceutical and agrochemical research. Its aldehyde and terminal alkyne functional groups allow it to participate in a variety of transformations, including Wittig reactions, nucleophilic additions, and metal-catalyzed couplings such as Sonogashira and click chemistry. This dual reactivity makes it valuable for constructing carbon-carbon bonds and introducing functionalized side chains. It is also employed in the synthesis of natural products and bioactive compounds where a five-carbon chain with both unsaturation and reactivity is required. Its versatility in multistep syntheses enhances its utility in medicinal chemistry and materials science.

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