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173436-86-7

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173436-86-7 Usage

General Description

(RS)-2-(3'-iodophenyl)propanoic acid is a chemical compound with the molecular formula C9H9IO2. It is a chiral compound with two possible enantiomers, (R)- and (S)-2-(3'-iodophenyl)propanoic acid. (RS)-2-(3'-iodophenyl)propanoic acid is a derivative of phenylpropanoic acid and contains a phenyl group with an iodine substituent. It has potential applications in organic synthesis and pharmaceutical research due to its structural features and reactivity. Additionally, it may be used as a precursor for the synthesis of various biologically active compounds. The precise properties and potential uses of (RS)-2-(3'-iodophenyl)propanoic acid would depend on its specific enantiomeric form.

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.

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