(S)-[(1-Phenylethyl)amino]acetic Acid

≥97%

Reagent Code: #57177
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CAS Number 78397-14-5

science Other reagents with same CAS 78397-14-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 179.22 g/mol
Formula C₁₀H₁₃NO₂
badge Registry Numbers
MDL Number MFCD11656778
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block or intermediate. Its structure, featuring a chiral center and functional groups like the amino and carboxylic acid, makes it valuable for the preparation of enantiomerically pure compounds. It is often employed in the synthesis of pharmaceuticals, particularly in the development of drugs that require specific stereochemistry for enhanced efficacy or reduced side effects. Additionally, it can be used in the production of ligands for asymmetric catalysis, aiding in the creation of complex molecules with high enantioselectivity. Its application extends to research and development in medicinal chemistry, where it contributes to the design and optimization of bioactive molecules.

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Test Parameter Specification
Appearance White solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿11,574.00

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(S)-[(1-Phenylethyl)amino]acetic Acid
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This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block or intermediate. Its structure, featuring a chiral center and functional groups like the amino and carboxylic acid, makes it valuable for the preparation of enantiomerically pure compounds. It is often employed in the synthesis of pharmaceuticals, particularly in the development of drugs that require specific stereochemistry for enhanced efficacy or reduced side effects. Additionally, it can

This compound is primarily utilized in the field of organic synthesis, where it serves as a chiral building block or intermediate. Its structure, featuring a chiral center and functional groups like the amino and carboxylic acid, makes it valuable for the preparation of enantiomerically pure compounds. It is often employed in the synthesis of pharmaceuticals, particularly in the development of drugs that require specific stereochemistry for enhanced efficacy or reduced side effects. Additionally, it can be used in the production of ligands for asymmetric catalysis, aiding in the creation of complex molecules with high enantioselectivity. Its application extends to research and development in medicinal chemistry, where it contributes to the design and optimization of bioactive molecules.

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