(S)-methyl 2-(4-butylphenyl)propanoate

Reagent Code: #38607
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CAS Number 404354-75-2

science Other reagents with same CAS 404354-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.31 g/mol
Formula C₁₄H₂₀O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily used in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a butylphenyl group and a propanoate ester, makes it valuable in the development of enantiomerically pure drugs, particularly those targeting inflammation or pain. The chiral center allows for the creation of specific stereoisomers, which can enhance the efficacy and reduce the side effects of therapeutic agents. Additionally, it may serve as an intermediate in the production of liquid crystal materials, contributing to the development of advanced display technologies. Its applications are often centered around its role in fine chemical synthesis and its potential in designing biologically active compounds.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿9,000.00

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(S)-methyl 2-(4-butylphenyl)propanoate
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This compound is primarily used in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a butylphenyl group and a propanoate ester, makes it valuable in the development of enantiomerically pure drugs, particularly those targeting inflammation or pain. The chiral center allows for the creation of specific stereoisomers, which can enhance the efficacy and reduce the side effects of therapeutic agents. Additional

This compound is primarily used in the pharmaceutical and chemical research industries as a chiral building block for the synthesis of more complex molecules. Its structure, featuring a butylphenyl group and a propanoate ester, makes it valuable in the development of enantiomerically pure drugs, particularly those targeting inflammation or pain. The chiral center allows for the creation of specific stereoisomers, which can enhance the efficacy and reduce the side effects of therapeutic agents. Additionally, it may serve as an intermediate in the production of liquid crystal materials, contributing to the development of advanced display technologies. Its applications are often centered around its role in fine chemical synthesis and its potential in designing biologically active compounds.

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