173436-86-7 Usage
Description
(RS)-2-(3'-iodophenyl)propanoic acid, with the molecular formula C9H9IO2, is a chiral chemical compound that exists in two possible enantiomers, (R)and (S)-2-(3'-iodophenyl)propanoic acid. It is a derivative of phenylpropanoic acid, featuring a phenyl group with an iodine substituent. (RS)-2-(3'-iodophenyl)propanoic acid holds potential in the realms of organic synthesis and pharmaceutical research, with its specific properties and applications varying depending on the enantiomeric form.
Uses
Used in Organic Synthesis:
(RS)-2-(3'-iodophenyl)propanoic acid is used as a building block for the synthesis of various complex organic molecules. Its unique structural features and reactivity make it a valuable component in creating novel compounds with specific functionalities.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (RS)-2-(3'-iodophenyl)propanoic acid is utilized as a precursor for the development of biologically active compounds. Its structural diversity and potential for enantiomeric differentiation allow for the creation of new drugs with targeted therapeutic effects.
Used in Chiral Chemistry:
(RS)-2-(3'-iodophenyl)propanoic acid is employed in chiral chemistry to study the differences between its enantiomers, (R)and (S)-2-(3'-iodophenyl)propanoic acid. Understanding these differences is crucial for the development of enantiomerically pure drugs, which can have significant implications for their efficacy and safety profiles.
Used in Radiopharmaceuticals:
Given the presence of an iodine atom, (RS)-2-(3'-iodophenyl)propanoic acid may also find applications in the field of radiopharmaceuticals, where it could be used as a starting material for the development of radiolabeled compounds for imaging and therapeutic purposes.
Used in Chemical Reagents:
(RS)-2-(3'-iodophenyl)propanoic acid can be used as a reagent in various chemical reactions, taking advantage of its unique structural features to facilitate specific transformations or to introduce desired functional groups into target molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 173436-86-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,3,4,3 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 173436-86:
(8*1)+(7*7)+(6*3)+(5*4)+(4*3)+(3*6)+(2*8)+(1*6)=147
147 % 10 = 7
So 173436-86-7 is a valid CAS Registry Number.
173436-86-7Relevant 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.
