2-phenylacetamide CAS 103-81-1 Product parameters

Synonyms

2-phenylacetamide CAS 103-81-1 Storage

Store 2-phenylacetamide in a cool, dry place away from heat and direct sunlight. Ideal storage temperatures are usually below 77°F (25°C) to maintain its stability.

2 phenylacetamide uses

2-Phenylacetamide, also known as alpha-phenylacetamide, has several uses in various fields. Here are some common applications of 2-phenylacetamide:

1. Pharmaceutical Intermediates: 2-Phenylacetamide is widely employed as an intermediate in the synthesis of various pharmaceutical compounds. It serves as a building block for the preparation of drugs and active pharmaceutical ingredients (APIs).
2. Chemical Research: It is utilized in chemical research and development as a starting material for the synthesis of diverse organic compounds. Its versatile nature allows for the creation of new molecules with potentially valuable properties.
3. Organic Synthesis: 2-Phenylacetamide participates in a range of organic synthesis reactions, including acylation, amidation, and condensation reactions. It can be modified to introduce different functional groups and create novel compounds.
4. Industrial Applications: The compound finds use in various industrial applications, such as the production of dyes, pigments, and fragrances. Its chemical properties make it suitable for incorporation into these products.
5. Solvent: 2-Phenylacetamide can act as a solvent for certain substances, facilitating dissolution and reaction processes in laboratories and industries.
6. Research Chemical: Researchers may utilize 2-phenylacetamide as a reference compound or standard in analytical techniques, such as chromatography or spectroscopy, to identify and quantify other substances.
7. Agrochemicals: It is involved in the synthesis of certain agrochemicals, including pesticides and herbicides, which are used to protect crops from pests and weeds.

2-phenylacetamide with thionyl chloride

To convert 2-phenylacetamide into its corresponding compound, thionyl chloride is utilized. This process involves the formation of sulfonyl chloride, which subsequently reacts with 2-phenylacetamide. The reaction takes place through a nucleophilic substitution, resulting in the formation of a new compound. Thionyl chloride acts as a reagent, facilitating the conversion by providing the necessary chemical environment. This method allows for the modification of the molecular structure of 2-phenylacetamide, enabling the synthesis of diverse compounds with potential applications in various fields.