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MilliporeSigma

M19007

3-Methoxyphenylacetic acid

≥99%

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About This Item

Linear Formula:
CH3OC6H4CH2CO2H
CAS Number:
1798-09-0
Molecular Weight:
166.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24896705
EC Number:
217-282-8
Beilstein/REAXYS Number:
2614004
MDL number:
MFCD00004334

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Product Name

3-Methoxyphenylacetic acid, ≥99%

InChI key

LEGPZHPSIPPYIO-UHFFFAOYSA-N

InChI

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

SMILES string

COc1cccc(CC(O)=O)c1

assay

≥99%

mp

65-69 °C (lit.)

Quality Level

100

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1 of 4

This Item
H49901P16001261793
3-Methoxyphenylacetic acid ≥99%

Sigma-Aldrich

M19007

3-Methoxyphenylacetic acid

3-Hydroxyphenylacetic acid ≥99%

Sigma-Aldrich

H49901

3-Hydroxyphenylacetic acid

3-Phenoxypropionic acid 99%

Sigma-Aldrich

P16001

3-Phenoxypropionic acid

3-Benzoylbenzoic acid 99%

Sigma-Aldrich

261793

3-Benzoylbenzoic acid

assay

≥99%

assay

≥99%

assay

99%

assay

99%

Quality Level

100

Quality Level

100

Quality Level

100

Quality Level

100

mp

65-69 °C (lit.)

mp

129-133 °C (lit.)

mp

98-100 °C (lit.)

mp

164-166 °C (lit.)

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H318

Hazard Classifications

Eye Dam. 1

Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBC0491V
S62586V
S62586
S46182
13214AJ

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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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