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CAS

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151957-59-4

(S)-2-(3'-iodophenyl)propanoic acid, with the chemical formula C9H9IO2, is a derivative of the essential amino acid phenylalanine, featuring an additional iodine atom. (S)-2-(3'-iodophenyl)propanoic acid has been the subject of research for its potential pharmacological properties, particularly in the treatment of neurological disorders and inflammation. It is also being investigated for its role in the development of radioiodinated ligands for imaging and diagnostic applications. While its precise uses and biological effects are still under exploration, (S)-2-(3'-iodophenyl)propanoic acid holds promise for a range of medical and research purposes.

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  • 151957-59-4 Structure

  • Basic information

    1. Product Name: (S)-2-(3'-iodophenyl)propanoic acid
    2. Synonyms: (S)-2-(3'-iodophenyl)propanoic acid
    3. CAS NO:151957-59-4
    4. Molecular Formula:
    5. Molecular Weight: 276.074
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 151957-59-4.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-2-(3'-iodophenyl)propanoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-2-(3'-iodophenyl)propanoic acid(151957-59-4)
    11. EPA Substance Registry System: (S)-2-(3'-iodophenyl)propanoic acid(151957-59-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 151957-59-4(Hazardous Substances Data)

151957-59-4 Usage

Uses

Used in Pharmaceutical Applications:
(S)-2-(3'-iodophenyl)propanoic acid is used as a potential therapeutic agent for neurological disorders due to its pharmacological properties. It is being studied for its effects on neurological conditions, which may include the treatment of various brain-related diseases and disorders.
Used in Anti-Inflammatory Applications:
As an anti-inflammatory agent, (S)-2-(3'-iodophenyl)propanoic acid is used to potentially alleviate inflammation, which can be a component of numerous health issues, including autoimmune diseases and tissue damage.
Used in Diagnostic Imaging:
(S)-2-(3'-iodophenyl)propanoic acid is used as a precursor in the development of radioiodinated ligands, which are essential for imaging and diagnostic purposes. These ligands can help visualize and diagnose various conditions within the body, particularly those related to the central nervous system.
Used in Research and Development:
In the field of research and development, (S)-2-(3'-iodophenyl)propanoic acid serves as a valuable compound for exploring new avenues in medicine and pharmaceuticals. Its unique properties and potential applications make it a subject of interest for scientists working on innovative treatments and diagnostic tools.

Check Digit Verification of cas no

The CAS Registry Mumber 151957-59-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,9,5 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 151957-59:
(8*1)+(7*5)+(6*1)+(5*9)+(4*5)+(3*7)+(2*5)+(1*9)=154
154 % 10 = 4
So 151957-59-4 is a valid CAS Registry Number.

151957-59-4Relevant articles and documents

Enantioselective syntheses of 2-arylpropanoic acid non-steroidal antiinflammatory drugs and related compounds

Hamon, David P.G.,Massy-Westropp, Ralph A.,Newton, Josephine L.

, p. 12645 - 12660 (2007/10/02)

(S)-2-[4′-(2″-Methylpropyl)phenylpropanoic acid (ibuprofen) and (S)-2-(3′-benzoylphenyl)propanoic acid (ketoprofen) have been synthesised in high enantiomeric excess. Control of stereochemistry was achieved by a combination of Sharpless epoxidalion followed by catalytic hydrogenolysis of the introduced benzylic epoxide oxygen bond. Also, the coupling of organic compounds in the presence of palladium with enantiopure 2-(3-iodophenyl)propanoic and 2-(4-iodophenyl)propanoic acids, prepared by the methodology above, is a general method for the synthesis of optically active arylpropanoic acids.

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