(R)-2-Acetamido-2-phenylacetic acid

≥95%

Reagent Code: #37528
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CAS Number 14257-84-2

science Other reagents with same CAS 14257-84-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.20 g/mol
Formula C₁₀H₁₁NO₃
badge Registry Numbers
MDL Number MFCD12795908
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. It plays a crucial role in the production of enantiomerically pure pharmaceuticals, particularly in the development of antibiotics and anti-inflammatory medications. Its chiral nature allows for the creation of more effective and targeted therapies with reduced side effects. Additionally, it is employed in research and development for studying enzyme interactions and chiral resolution processes, aiding in the advancement of medicinal chemistry and drug design.

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Test Parameter Specification
Appearance White Solid
Purity 94.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿390.00
inventory 250mg
10-20 days ฿780.00

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(R)-2-Acetamido-2-phenylacetic acid
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This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. It plays a crucial role in the production of enantiomerically pure pharmaceuticals, particularly in the development of antibiotics and anti-inflammatory medications. Its chiral nature allows for the creation of more effective and targeted therapies with reduced side effects. Additionally, it is employed in research and development for studying enzyme interactions and chiral re

This compound is primarily utilized in the pharmaceutical industry as a chiral building block for the synthesis of various drugs. It plays a crucial role in the production of enantiomerically pure pharmaceuticals, particularly in the development of antibiotics and anti-inflammatory medications. Its chiral nature allows for the creation of more effective and targeted therapies with reduced side effects. Additionally, it is employed in research and development for studying enzyme interactions and chiral resolution processes, aiding in the advancement of medicinal chemistry and drug design.

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