(S)-()-2-Phenylbutyric acid

99%

Reagent Code: #113620
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CAS Number 4286-15-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 164.20 g/mol
Formula C₁₀H₁₂O₂
badge Registry Numbers
MDL Number MFCD00063164
thermostat Physical Properties
Boiling Point 98-100 °C0.3 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.055 g/mL at 25 °C(lit.)
Storage 2-8°C, sealed, dry

description Product Description

(S)-()-2-Phenylbutyric acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for developing drugs with specific therapeutic effects. In addition to pharmaceuticals, it finds application in organic synthesis, where it serves as a building block for creating complex molecules. Its phenyl group and carboxylic acid functionality allow it to participate in a range of chemical reactions, including esterification, amidation, and coupling reactions. Furthermore, it is used in research and development for studying stereochemistry and designing new chemical entities with potential biological activity. Its role in asymmetric synthesis is particularly noteworthy, as it aids in the production of compounds with high enantiomeric purity, which is crucial in many therapeutic applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,275.00
inventory 5g
10-20 days ฿16,992.00
(S)-()-2-Phenylbutyric acid
(S)-()-2-Phenylbutyric acid is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various active pharmaceutical ingredients (APIs). Its chiral structure makes it valuable in the production of enantiomerically pure compounds, which are essential for developing drugs with specific therapeutic effects. In addition to pharmaceuticals, it finds application in organic synthesis, where it serves as a building block for creating complex molecules. Its phenyl group and carboxylic acid functionality allow it to participate in a range of chemical reactions, including esterification, amidation, and coupling reactions. Furthermore, it is used in research and development for studying stereochemistry and designing new chemical entities with potential biological activity. Its role in asymmetric synthesis is particularly noteworthy, as it aids in the production of compounds with high enantiomeric purity, which is crucial in many therapeutic applications.
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