N-Benzoylisopropylamine

97%

Reagent Code: #219491
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CAS Number 5440-69-7

science Other reagents with same CAS 5440-69-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.22 g/mol
Formula C₁₀H₁₃NO
thermostat Physical Properties
Melting Point 100-101 °C
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the preparation of active pharmaceutical ingredients. It serves as a building block in the development of analgesic and anti-inflammatory compounds due to its amide structure and aromatic substitution pattern. Its lipophilic character makes it suitable for modifying drug penetration and stability. Also employed in the synthesis of agrochemicals and specialty polymers where controlled steric hindrance and electronic effects are required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,870.00
inventory 250mg
10-20 days ฿3,720.00

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N-Benzoylisopropylamine
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Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the preparation of active pharmaceutical ingredients. It serves as a building block in the development of analgesic and anti-inflammatory compounds due to its amide structure and aromatic substitution pattern. Its lipophilic character makes it suitable for modifying drug penetration and stability. Also employed in the synthesis of agrochemicals and specialty polymers where controlled steric hindrance a

Used primarily as an intermediate in organic synthesis, particularly in the pharmaceutical industry for the preparation of active pharmaceutical ingredients. It serves as a building block in the development of analgesic and anti-inflammatory compounds due to its amide structure and aromatic substitution pattern. Its lipophilic character makes it suitable for modifying drug penetration and stability. Also employed in the synthesis of agrochemicals and specialty polymers where controlled steric hindrance and electronic effects are required.

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