C-(6-Chloro-naphthalen-2-yl)-methylamine

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Reagent Code: #163091
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CAS Number 1261453-93-3

science Other reagents with same CAS 1261453-93-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.66 g/mol
Formula C₁₁H₁₀ClN
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MDL Number MFCD18410075
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of naproxen, a widely prescribed medication for pain, inflammation, and arthritis. Its structure allows for efficient derivatization to form active pharmaceutical ingredients. Also employed in research for developing new chiral compounds due to its amine functionality, which supports asymmetric synthesis. Additionally, it serves as a building block in agrochemicals and specialty polymers where aromatic and amine groups enhance material stability and reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,550.00

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C-(6-Chloro-naphthalen-2-yl)-methylamine
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Used as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of naproxen, a widely prescribed medication for pain, inflammation, and arthritis. Its structure allows for efficient derivatization to form active pharmaceutical ingredients. Also employed in research for developing new chiral compounds due to its amine functionality, which supports asymmetric synthesis. Additionally, it serves as a building block in agrochemicals and specialty polym

Used as an intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs), particularly in the production of naproxen, a widely prescribed medication for pain, inflammation, and arthritis. Its structure allows for efficient derivatization to form active pharmaceutical ingredients. Also employed in research for developing new chiral compounds due to its amine functionality, which supports asymmetric synthesis. Additionally, it serves as a building block in agrochemicals and specialty polymers where aromatic and amine groups enhance material stability and reactivity.

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