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Documentos

M19007

Sigma-Aldrich

3-Methoxyphenylacetic acid

≥99%

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About This Item

Fórmula lineal:
CH3OC6H4CH2CO2H
Número de CAS:
1798-09-0
Peso molecular:
166.17
Beilstein/REAXYS Number:
2614004
EC Number:
217-282-8
MDL number:
MFCD00004334
UNSPSC Code:
12352100
PubChem Substance ID:
24896705
NACRES:
NA.22

Quality Level

100

assay

≥99%

mp

65-69 °C (lit.)

SMILES string

COc1cccc(CC(O)=O)c1

InChI

1S/C9H10O3/c1-12-8-4-2-3-7(5-8)6-9(10)11/h2-5H,6H2,1H3,(H,10,11)

InChI key

LEGPZHPSIPPYIO-UHFFFAOYSA-N

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pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Georgios I Panoutsopoulos et al.
Chemical research in toxicology, 17(10), 1368-1376 (2004-10-19)
Aliphatic aldehydes have a high affinity toward aldehyde dehydrogenase activity but are relatively poor substrates of aldehyde oxidase and xanthine oxidase. In addition, the oxidation of xenobiotic-derived aromatic aldehydes by the latter enzymes has not been studied to any great
Bohang Zhou et al.
European journal of medicinal chemistry, 200, 112415-112415 (2020-05-27)
As simple analogues of the natural compound chelerythrine, a novel anti-cholinesterase 2-phenylisoquinolin-2-ium scaffold was designed by structure imitation. The activity evaluation led to the discovery of seven compounds with potent anti-acetylcholinesterase activity with IC50 values of ≤0.72 μM, superior to chelerythrine
Ramisetti Nageswara Rao et al.
Chirality, 24(4), 339-344 (2012-02-22)
(R)-(-)-α-Methoxy phenyl acetic acid, (S)-(-)-1,1'-(2-naphthol), and (R)-(+)-α-methoxy-α-trifluoromethyl phenyl acetic acid were evaluated as chiral shift reagents (CSRs) for (1)H NMR spectroscopic resolution and determination of R and S enantiomers of modafinil (MDL) in bulk drugs and formulations. Effects of the
M Chen et al.
Antimicrobial agents and chemotherapy, 45(7), 2023-2029 (2001-06-16)
Our previous studies have shown that chalcones exhibit potent antileishmanial and antimalarial activities in vitro and in vivo. Preliminary studies showed that these compounds destroyed the ultrastructure of Leishmania parasite mitochondria and inhibited the respiration and the activity of mitochondrial
Phytotoxins in Rhizoctonia solani: isolation and biological activity of m-hydroxy- and m-methoxyphenylacetic acids.
N B Mandava et al.
Journal of agricultural and food chemistry, 28(1), 71-75 (1980-01-01)
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