3-Cyano-3-phenylpropanoic acid

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Reagent Code: #55687
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CAS Number 14387-18-9

science Other reagents with same CAS 14387-18-9

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Weight 175.1840 g/mol
Formula C₁₀H₉NO₂
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MDL Number MFCD03032627
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3-Cyano-3-phenylpropanoic acid is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and fine chemicals. Its structure, featuring both a cyano group and a carboxylic acid, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the preparation of compounds with potential biological activity, such as inhibitors or modulators of enzymes and receptors. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry. The compound’s reactivity allows for further functionalization, enabling the creation of diverse chemical entities for research and development purposes.

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inventory 250mg
10-20 days ฿1,719.00

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3-Cyano-3-phenylpropanoic acid
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3-Cyano-3-phenylpropanoic acid is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and fine chemicals. Its structure, featuring both a cyano group and a carboxylic acid, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the preparation of compounds with potential biological activity, such as inhibitors or modulators of enzymes and receptors. Additionally, it serves as a precursor in the synthesis of heter

3-Cyano-3-phenylpropanoic acid is primarily used in organic synthesis as an intermediate for the production of various pharmaceuticals and fine chemicals. Its structure, featuring both a cyano group and a carboxylic acid, makes it a versatile building block in the synthesis of complex molecules. It is often employed in the preparation of compounds with potential biological activity, such as inhibitors or modulators of enzymes and receptors. Additionally, it serves as a precursor in the synthesis of heterocyclic compounds, which are widely used in medicinal chemistry. The compound’s reactivity allows for further functionalization, enabling the creation of diverse chemical entities for research and development purposes.

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