4-Methylhex-1-yn-3-amine hydrochloride

95%

Reagent Code: #132164
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CAS Number 2703752-14-9

science Other reagents with same CAS 2703752-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 147.65 g/mol
Formula C₇H₁₄ClN
badge Registry Numbers
MDL Number MFCD34186975
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used primarily as a chemical intermediate in organic synthesis, this compound plays a role in the preparation of pharmaceuticals and biologically active molecules. Its alkyne and amine functional groups make it valuable for constructing complex molecular frameworks through coupling reactions and nucleophilic additions. It is also employed in research settings for the development of novel amine-containing compounds, including potential neuroactive agents. Due to its hydrochloride salt form, it exhibits improved stability and solubility, facilitating handling and use in aqueous or polar environments.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿16,740.00
inventory 100mg
10-20 days ฿26,770.00
inventory 250mg
10-20 days ฿40,150.00

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4-Methylhex-1-yn-3-amine hydrochloride
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Used primarily as a chemical intermediate in organic synthesis, this compound plays a role in the preparation of pharmaceuticals and biologically active molecules. Its alkyne and amine functional groups make it valuable for constructing complex molecular frameworks through coupling reactions and nucleophilic additions. It is also employed in research settings for the development of novel amine-containing compounds, including potential neuroactive agents. Due to its hydrochloride salt form, it exhibits im

Used primarily as a chemical intermediate in organic synthesis, this compound plays a role in the preparation of pharmaceuticals and biologically active molecules. Its alkyne and amine functional groups make it valuable for constructing complex molecular frameworks through coupling reactions and nucleophilic additions. It is also employed in research settings for the development of novel amine-containing compounds, including potential neuroactive agents. Due to its hydrochloride salt form, it exhibits improved stability and solubility, facilitating handling and use in aqueous or polar environments.

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