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7021-09-2-Methoxyphenylacetic acid Methoxyphenylacetic acid

Methoxyphenylacetic acid

For research use only. Not for therapeutic Use.

  • CAT Number: M018256
  • CAS Number: 7021-09-2
  • Molecular Formula: C9H10O3
  • Molecular Weight: 166.176
  • Purity: ≥95%
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Related Small Molecules: 6,7-Demethylene-6,7-dehydro Drospirenone     (4-Butyl[1,1-biphenyl]-4-yl)-boronic acid     diethoxysilane    

Methoxyphenylacetic acid (Cat.No:M018256) is an organic compound with a methoxyphenyl group and an acetic acid moiety. It is used as an intermediate in the synthesis of various pharmaceutical and chemical compounds. Methoxyphenylacetic acid plays a role in the creation of molecules with diverse applications in industry and research.


Catalog Number M018256
CAS Number 7021-09-2
Synonyms

(+/-)-ALPHA-METHOXYPHENYLACETIC ACID;ALPHA-METHOXYPHENYLACETIC ACID;2-METHOXY-2-PHENYLACETIC ACID;DL-O-METHYLMANDELIC ACID;DL-METHOXYPHENYLACETIC ACID;DL-A-METHOXYPHENYLACETIC ACID;DL-ALPHA-METHOXYPHENYLACETIC ACID;O-METHYL-DL-MANDELIC ACID

Molecular Formula C9H10O3
Purity ≥95%
Storage Room Temperature
IUPAC Name 2-methoxy-2-phenylacetic acid
InChI InChI=1S/C9H10O3/c1-12-8(9(10)11)7-5-3-2-4-6-7/h2-6,8H,1H3,(H,10,11)
InChIKey DIWVBIXQCNRCFE-UHFFFAOYSA-N
SMILES COC(C1=CC=CC=C1)C(=O)O
Reference

1: Bünnemann K, Merten C. Solvation of a chiral carboxylic acid: effects of
hydrogen bonding on the IR and VCD spectra of α-methoxyphenylacetic acid. Phys
Chem Chem Phys. 2017 Jul 26;19(29):18948-18956. doi: 10.1039/c7cp02049j. PubMed
PMID: 28650488.
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2: Sadeghian H, Attaran N, Jafari Z, Saberi MR, Seyedi SM, Eshghi H, Pordel M,
Riazi MM. Design and synthesis of 4-methoxyphenylacetic acid esters as
15-lipoxygenase inhibitors and SAR comparative studies of them. Bioorg Med Chem.
2009 Mar 15;17(6):2327-35. doi: 10.1016/j.bmc.2009.02.009. Epub 2009 Feb 13.
Erratum in: Bioorg Med Chem. 2010 Jan 1;18(1):462. Seyedi, Seyed Mohammad
[added]; Eshghi, Hossein [added]. PubMed PMID: 19251422.
<br>

3: Chen J, Zheng YG, Shen YC. Biotransformation of p-methoxyphenylacetonitrile
into p-methoxyphenylacetic acid by resting cells of Bacillus subtilis. Biotechnol
Appl Biochem. 2008 Jul;50(Pt 3):147-53. PubMed PMID: 17910534.
<br>

4: Rao RN, Nagaraju D, Parimala P, Adapa SR, Alam MM. Development and
substantiation of a liquid chromatographic method for monitoring organic
reactions involved in synthesis of 4-methoxyphenylacetic acid. J Chromatogr A.
2002 Oct 4;972(2):277-82. PubMed PMID: 12416886.
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5: García R, Seco JM, Vázquez SA, Qui&#241;oá E, Riguera R. Absolute configuration of
secondary alcohols by 1H NMR: in situ complexation of alpha-methoxyphenylacetic
acid esters with barium(II). J Org Chem. 2002 Jun 28;67(13):4579-89. PubMed PMID:
12076161.
<br>

6: Yi YH, Liao WP, Lu X. Simultaneous determination of tryptophan,
5-hydroxytryptophan, 5-hydroxytryptamine, 5-hydroxyindoleacetic acid,
4-hydroxy-3-methoxyphenylacetic acid and 3-methoxy-4-hydroxyphenylglycol in human
cerebrospinal fluid. J Chromatogr B Biomed Appl. 1994 Nov 4;661(1):143-8. PubMed
PMID: 7532522.
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7: Husain PA, Colbert JE, Sirimanne SR, VanDerveer DG, Herman HH, May SW.
N-succinimidyl methoxyphenylacetic acid ester, an amine-directed chiral
derivatizing reagent suitable for enzymatic scale resolutions. Anal Biochem. 1989
Apr;178(1):177-83. PubMed PMID: 2729571.

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