(S)-2-m-Tolyl-propionic acid

95%

Reagent Code: #38350
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CAS Number 601472-22-4

science Other reagents with same CAS 601472-22-4

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Weight 164.2011 g/mol
Formula C₁₀H₁₂O₂
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MDL Number MFCD20641860
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(S)-2-m-Tolyl-propionic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs). Its chiral structure makes it valuable for producing enantiomerically pure compounds, which are essential for developing medications with higher efficacy and fewer side effects. Additionally, it is employed in organic synthesis for constructing complex molecules, particularly in the preparation of fine chemicals and active pharmaceutical ingredients (APIs). Its applications also extend to research and development, where it serves as a building block for studying structure-activity relationships in drug design.

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inventory 100mg
10-20 days ฿5,832.00

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(S)-2-m-Tolyl-propionic acid
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(S)-2-m-Tolyl-propionic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs). Its chiral structure makes it valuable for producing enantiomerically pure compounds, which are essential for developing medications with higher efficacy and fewer side effects. Additionally, it is employed in organic synthesis for constructing complex molecules, particularly in the preparation of fine chemicals and active pharmaceutica

(S)-2-m-Tolyl-propionic acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of nonsteroidal anti-inflammatory drugs (NSAIDs). Its chiral structure makes it valuable for producing enantiomerically pure compounds, which are essential for developing medications with higher efficacy and fewer side effects. Additionally, it is employed in organic synthesis for constructing complex molecules, particularly in the preparation of fine chemicals and active pharmaceutical ingredients (APIs). Its applications also extend to research and development, where it serves as a building block for studying structure-activity relationships in drug design.

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