N-(Prop-2-yn-1-yl)cyclohexanamine

95%

Reagent Code: #215714
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CAS Number 18292-76-7

science Other reagents with same CAS 18292-76-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.22 g/mol
Formula C₉H₁₅N
badge Registry Numbers
MDL Number MFCD02731102
thermostat Physical Properties
Boiling Point 98-100 °C at 30 mmHg
inventory_2 Storage & Handling
Density 0.9112 g/cm3
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and bioconjugation. The secondary amine group enables further derivatization, useful in building complex nitrogen-containing molecules. Also employed in the development of functional materials and ligands for catalysis.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,280.00
250mg
10-20 days ฿15,770.00
1g
10-20 days ฿42,560.00
N-(Prop-2-yn-1-yl)cyclohexanamine
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and bioconjugation. The secondary amine group enables further derivatization, useful in building complex nitrogen-containing molecules. Also employed in the development of functional materials and ligands for catalysis.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its alkyne functionality allows participation in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), making it valuable in drug discovery and bioconjugation. The secondary amine group enables further derivatization, useful in building complex nitrogen-containing molecules. Also employed in the development of functional materials and ligands for catalysis.

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