(R)-N-(1-Phenylethyl)acetamide

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Reagent Code: #37745
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CAS Number 36283-44-0

science Other reagents with same CAS 36283-44-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 163.2163 g/mol
Formula C₁₀H₁₃NO
badge Registry Numbers
MDL Number MFCD03427633
thermostat Physical Properties
Melting Point 102 °C
Boiling Point 327.932 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.008g/cm3
Storage room temperature

description Product Description

Used in the synthesis of chiral compounds, particularly in pharmaceutical research where enantiomeric purity is crucial. It serves as an intermediate in the production of optically active drugs, aiding in the development of medications with improved efficacy and reduced side effects. Additionally, it is utilized in asymmetric synthesis to create complex molecules with specific stereochemistry, which is essential in the fields of agrochemicals and fine chemicals. Its role in chiral resolution processes helps separate enantiomers, ensuring high purity in the final product.

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inventory 1g
10-20 days ฿513.00

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(R)-N-(1-Phenylethyl)acetamide
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Used in the synthesis of chiral compounds, particularly in pharmaceutical research where enantiomeric purity is crucial. It serves as an intermediate in the production of optically active drugs, aiding in the development of medications with improved efficacy and reduced side effects. Additionally, it is utilized in asymmetric synthesis to create complex molecules with specific stereochemistry, which is essential in the fields of agrochemicals and fine chemicals. Its role in chiral resolution processes he

Used in the synthesis of chiral compounds, particularly in pharmaceutical research where enantiomeric purity is crucial. It serves as an intermediate in the production of optically active drugs, aiding in the development of medications with improved efficacy and reduced side effects. Additionally, it is utilized in asymmetric synthesis to create complex molecules with specific stereochemistry, which is essential in the fields of agrochemicals and fine chemicals. Its role in chiral resolution processes helps separate enantiomers, ensuring high purity in the final product.

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