1-Phenyl-1-hexyne

≥98%

Reagent Code: #114931
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CAS Number 1129-65-3

science Other reagents with same CAS 1129-65-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.24 g/mol
Formula C₁₂H₁₄
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MDL Number MFCD00039969
inventory_2 Storage & Handling
Storage room temperature

description Product Description

1-Phenyl-1-hexyne is primarily used in organic synthesis as a building block for more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its alkyne functional group makes it valuable in click chemistry reactions, particularly in the formation of triazoles, which are important in drug discovery and material science. Additionally, it is utilized in the synthesis of conjugated polymers and organic electronic materials due to its ability to participate in polymerization reactions. In research, it is often employed to study reaction mechanisms involving alkynes and to develop new catalytic processes.

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Test Parameter Specification
Appearance Colorless to pale yellow clear liquid
Purity (%) 98
Specific Gravity (20/20) 0.9020-0.9040
Refractive Index (N20/D) 1.5330-1.5360

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25ml
10-20 days ฿19,880.00
inventory 1ml
10-20 days ฿1,640.00
inventory 5ml
10-20 days ฿5,800.00

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1-Phenyl-1-hexyne
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1-Phenyl-1-hexyne is primarily used in organic synthesis as a building block for more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its alkyne functional group makes it valuable in click chemistry reactions, particularly in the formation of triazoles, which are important in drug discovery and material science. Additionally, it is utilized in the synthesis of conjugated polymers and organic electronic materials due to its a

1-Phenyl-1-hexyne is primarily used in organic synthesis as a building block for more complex molecules. It serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its alkyne functional group makes it valuable in click chemistry reactions, particularly in the formation of triazoles, which are important in drug discovery and material science. Additionally, it is utilized in the synthesis of conjugated polymers and organic electronic materials due to its ability to participate in polymerization reactions. In research, it is often employed to study reaction mechanisms involving alkynes and to develop new catalytic processes.

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