(E)-5-Chloropent-1,3-diene

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Reagent Code: #184693
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CAS Number 40596-30-3

science Other reagents with same CAS 40596-30-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 102.56 g/mol
Formula C₅H₇Cl
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as a building block in organic synthesis, this compound serves in the preparation of more complex molecules for pharmaceuticals and agrochemicals. Its conjugated diene structure with a chlorine substituent allows participation in Diels-Alder reactions and other cycloadditions, making it valuable in constructing cyclic frameworks. It is also employed in cross-coupling reactions where the chlorine atom acts as a leaving group, enabling the formation of carbon-carbon bonds. Due to its reactivity, it is useful in research settings for developing novel intermediates and functionalized compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿8,990.00
inventory 1g
10-20 days ฿22,500.00

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(E)-5-Chloropent-1,3-diene
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Used primarily as a building block in organic synthesis, this compound serves in the preparation of more complex molecules for pharmaceuticals and agrochemicals. Its conjugated diene structure with a chlorine substituent allows participation in Diels-Alder reactions and other cycloadditions, making it valuable in constructing cyclic frameworks. It is also employed in cross-coupling reactions where the chlorine atom acts as a leaving group, enabling the formation of carbon-carbon bonds. Due to its reactiv

Used primarily as a building block in organic synthesis, this compound serves in the preparation of more complex molecules for pharmaceuticals and agrochemicals. Its conjugated diene structure with a chlorine substituent allows participation in Diels-Alder reactions and other cycloadditions, making it valuable in constructing cyclic frameworks. It is also employed in cross-coupling reactions where the chlorine atom acts as a leaving group, enabling the formation of carbon-carbon bonds. Due to its reactivity, it is useful in research settings for developing novel intermediates and functionalized compounds.

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