2-(4-Pentynyloxy)tetrahydro-2H-pyran

95%

Reagent Code: #226678
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CAS Number 62992-46-5

science Other reagents with same CAS 62992-46-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 168.23 g/mol
Formula C₁₀H₁₆O₂
badge Registry Numbers
MDL Number MFCD00792655
thermostat Physical Properties
Melting Point 84-88 °C (lit.)
inventory_2 Storage & Handling
Density 0.968 g/mL at 25 °C (lit.)
Storage 2-8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its alkyne functionality enables click chemistry reactions, making it valuable in the development of bioactive molecules and functional materials. Commonly employed in the preparation of complex molecules via coupling reactions, it facilitates the construction of carbon-carbon bonds in target compounds. Also utilized in research settings for modifying scaffolds in drug discovery programs.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿1,670.00
1g
10-20 days ฿4,880.00
5g
10-20 days ฿16,200.00
25g
10-20 days ฿73,840.00
2-(4-Pentynyloxy)tetrahydro-2H-pyran
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Used as a key intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its alkyne functionality enables click chemistry reactions, making it valuable in the development of bioactive molecules and functional materials. Commonly employed in the preparation of complex molecules via coupling reactions, it facilitates the construction of carbon-carbon bonds in target compounds. Also utilized in research settings for modifying scaffolds in drug discovery programs.

Used as a key intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its alkyne functionality enables click chemistry reactions, making it valuable in the development of bioactive molecules and functional materials. Commonly employed in the preparation of complex molecules via coupling reactions, it facilitates the construction of carbon-carbon bonds in target compounds. Also utilized in research settings for modifying scaffolds in drug discovery programs.

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