(E)-1-Phenyl-1-butene

97 %

Reagent Code: #182145
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CAS Number 1005-64-7

science Other reagents with same CAS 1005-64-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 132.21 g/mol
Formula C₁₀H₁₂
badge Registry Numbers
MDL Number MFCD00048708
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex aromatic and aliphatic systems. Its conjugated double bond structure makes it suitable for use in Heck reactions and other palladium-catalyzed coupling processes, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. It also finds use in research settings for studying stereochemical outcomes in addition reactions due to its defined E-configuration. Additionally, it can act as a model compound in kinetic studies involving radical reactions or isomerization processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,160.00
inventory 250mg
10-20 days ฿14,300.00
inventory 1g
10-20 days ฿42,900.00

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(E)-1-Phenyl-1-butene
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex aromatic and aliphatic systems. Its conjugated double bond structure makes it suitable for use in Heck reactions and other palladium-catalyzed coupling processes, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. It also finds use in research settings for studying stereochemical outcomes in addition reactions due to its defined E-configuration. Addi

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of more complex aromatic and aliphatic systems. Its conjugated double bond structure makes it suitable for use in Heck reactions and other palladium-catalyzed coupling processes, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical manufacturing. It also finds use in research settings for studying stereochemical outcomes in addition reactions due to its defined E-configuration. Additionally, it can act as a model compound in kinetic studies involving radical reactions or isomerization processes.

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