1448440-40-1

Basic information

• Product Name: (S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate
• Synonyms: (S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate
• CAS NO: 1448440-40-1
• Molecular Weight: 303.189
• Mol File: 1448440-40-1.mol

Chemical Properties

• CAS DataBase Reference: (S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate(1448440-40-1)
• EPA Substance Registry System: (S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate(1448440-40-1)

Safety Data

• Hazardous Substances Data: 1448440-40-1(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research and Development:
(S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate is used as a chemical compound in pharmaceutical research and development for its unique molecular structure and potential interactions with biological targets. The presence of fluorine atoms and the pyrrolidinone ring may contribute to its ability to modulate specific biological pathways or serve as a building block for the development of novel therapeutic agents.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate is used as a starting material or a synthetic intermediate for the design and synthesis of new drugs. Its structural features, including the amino acetyl group and the carbonitrile group, may be exploited to create molecules with specific biological activities, such as targeting enzymes, receptors, or other proteins involved in disease processes.
Used in Drug Design and Optimization:
(S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate is used as a structural element in drug design and optimization, where its unique features can be leveraged to improve the potency, selectivity, and pharmacokinetic properties of drug candidates. (S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate's fluorine-containing groups may also contribute to its ability to modulate protein-ligand interactions, potentially enhancing the efficacy of the resulting drug molecules.
Used in Chemical Synthesis:
(S)-1-(2-aminoacetyl)-4,4-difluoropyrrolidin-2-carbonitrile 2,2,2-trifluoroacetate is used as a reagent or a building block in chemical synthesis, particularly for the preparation of complex organic molecules with potential applications in various industries, including pharmaceuticals, agrochemicals, and materials science. Its versatile structure and functional groups make it a valuable component in the synthesis of novel compounds with tailored properties.