4-Benzoylbenzylamine hydrochloride

95%

Reagent Code: #141847
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CAS Number 53868-45-4

science Other reagents with same CAS 53868-45-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 247.7201 g/mol
Formula C₁₄H₁₄ClNO
badge Registry Numbers
MDL Number MFCD00216506
thermostat Physical Properties
Melting Point 128-132 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in organic reactions where an amine-functionalized benzophenone derivative is required. Its structure allows for easy modification in multi-step syntheses, making it valuable in medicinal chemistry research. Also employed in the preparation of photoinitiators and UV-curable resins due to the benzophenone moiety, which imparts photochemical stability and reactivity under UV light.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,400.00

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4-Benzoylbenzylamine hydrochloride
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in organic reactions where an amine-functionalized benzophenone derivative is required. Its structure allows for easy modification in multi-step syntheses, making it valuable in medicinal chemistry research. Also employed in the preparation of photoinitiators and UV-curable resins due to the benzophenone moiety, which imparts photoc

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anti-inflammatory and analgesic agents. It serves as a building block in organic reactions where an amine-functionalized benzophenone derivative is required. Its structure allows for easy modification in multi-step syntheses, making it valuable in medicinal chemistry research. Also employed in the preparation of photoinitiators and UV-curable resins due to the benzophenone moiety, which imparts photochemical stability and reactivity under UV light.

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