1-Phenyl-1-butyne

99%

Reagent Code: #224615
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Alias 1-phenyl-1-butyne
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CAS Number 622-76-4

science Other reagents with same CAS 622-76-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 130.19 g/mol
Formula C₁₀H₁₀
badge Registry Numbers
EC Number 210-752-3
MDL Number MFCD00039945
thermostat Physical Properties
Boiling Point 73-75 °C4 mm Hg(lit.)
inventory_2 Storage & Handling
Density 0.916 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its alkyne functionality allows for use in coupling reactions, such as Sonogashira or Cadiot-Chodkiewicz, enabling the construction of complex molecular structures. It is also employed in the development of specialty materials and research compounds where phenyl-substituted alkynes are required. Due to its reactivity, it finds niche applications in laboratory settings for synthesizing ketones, enynes, and other functionalized derivatives.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5g
10-20 days ฿1,790.00
25g
10-20 days ฿7,130.00
100g
10-20 days ฿26,310.00
1-Phenyl-1-butyne
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Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its alkyne functionality allows for use in coupling reactions, such as Sonogashira or Cadiot-Chodkiewicz, enabling the construction of complex molecular structures. It is also employed in the development of specialty materials and research compounds where phenyl-substituted alkynes are required. Due to its reactivity, it finds niche applications in laboratory settings for

Used primarily as an intermediate in organic synthesis, this compound serves in the preparation of pharmaceuticals and fine chemicals. Its alkyne functionality allows for use in coupling reactions, such as Sonogashira or Cadiot-Chodkiewicz, enabling the construction of complex molecular structures. It is also employed in the development of specialty materials and research compounds where phenyl-substituted alkynes are required. Due to its reactivity, it finds niche applications in laboratory settings for synthesizing ketones, enynes, and other functionalized derivatives.

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