4-Pentynoic Acid Methyl Ester

97%

Reagent Code: #83868
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CAS Number 21565-82-2

science Other reagents with same CAS 21565-82-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 112.1265 g/mol
Formula C₆H₈O₂
badge Registry Numbers
MDL Number MFCD12025043
thermostat Physical Properties
Boiling Point 101-102 °C(Press:175Torr)
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used in organic synthesis as a building block for more complex molecules. Commonly employed in click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition. It serves as a precursor in the production of pharmaceuticals and bioactive compounds. Also utilized in material science for the modification of polymers and surfaces to introduce alkyne functional groups. Its reactive alkyne moiety makes it valuable in bioconjugation techniques for labeling biomolecules.

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Test Parameter Specification
Appearance Colorless Liquid
Purity (%) 96.5-100
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,626.00
inventory 250mg
10-20 days ฿14,004.00

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4-Pentynoic Acid Methyl Ester
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Used in organic synthesis as a building block for more complex molecules. Commonly employed in click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition. It serves as a precursor in the production of pharmaceuticals and bioactive compounds. Also utilized in material science for the modification of polymers and surfaces to introduce alkyne functional groups. Its reactive alkyne moiety makes it valuable in bioconjugation techniques for labeling bi

Used in organic synthesis as a building block for more complex molecules. Commonly employed in click chemistry reactions, particularly in the formation of triazoles via copper-catalyzed azide-alkyne cycloaddition. It serves as a precursor in the production of pharmaceuticals and bioactive compounds. Also utilized in material science for the modification of polymers and surfaces to introduce alkyne functional groups. Its reactive alkyne moiety makes it valuable in bioconjugation techniques for labeling biomolecules.

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