N-Methylhex-5-en-1-amine hydrochloride

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Reagent Code: #72870
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CAS Number 862175-17-5

science Other reagents with same CAS 862175-17-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 149.67 g/mol
Formula C₇H₁₆ClN
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

N-Methylhex-5-en-1-amine hydrochloride is primarily utilized in organic synthesis as a versatile intermediate. It is commonly employed in the preparation of various pharmaceutical compounds, particularly those requiring the incorporation of an amine functional group. The compound’s structure, featuring both an amine and an alkene moiety, makes it valuable for reactions such as Michael additions, nucleophilic substitutions, and polymerizations. Additionally, it is used in the development of bioactive molecules and as a building block in the synthesis of complex organic frameworks. Its hydrochloride form ensures stability and ease of handling in laboratory settings.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,710.00
inventory 100mg
10-20 days ฿4,122.00

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N-Methylhex-5-en-1-amine hydrochloride
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N-Methylhex-5-en-1-amine hydrochloride is primarily utilized in organic synthesis as a versatile intermediate. It is commonly employed in the preparation of various pharmaceutical compounds, particularly those requiring the incorporation of an amine functional group. The compound’s structure, featuring both an amine and an alkene moiety, makes it valuable for reactions such as Michael additions, nucleophilic substitutions, and polymerizations. Additionally, it is used in the development of bioactive mole

N-Methylhex-5-en-1-amine hydrochloride is primarily utilized in organic synthesis as a versatile intermediate. It is commonly employed in the preparation of various pharmaceutical compounds, particularly those requiring the incorporation of an amine functional group. The compound’s structure, featuring both an amine and an alkene moiety, makes it valuable for reactions such as Michael additions, nucleophilic substitutions, and polymerizations. Additionally, it is used in the development of bioactive molecules and as a building block in the synthesis of complex organic frameworks. Its hydrochloride form ensures stability and ease of handling in laboratory settings.

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