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Merck
CN

W394300

o-Anisic acid

≥99%

Synonym(s):

2-Methoxybenzoic acid, O-Methylsalicylic acid, o-Anisic acid

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About This Item

Linear Formula:
CH3OC6H4CO2H
CAS Number:
Molecular Weight:
152.15
FEMA Number:
3943
PubChem Substance ID:
UNSPSC Code:
12164502
EC Number:
209-447-8
Beilstein/REAXYS Number:
509929
MDL number:
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biological source

synthetic

Quality Level

assay

≥99%

mp

98-100 °C (lit.)

application(s)

flavors and fragrances

SMILES string

COc1ccccc1C(O)=O

InChI

1S/C8H8O3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3,(H,9,10)

InChI key

ILUJQPXNXACGAN-UHFFFAOYSA-N

Other Notes

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Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

291.2 °F - closed cup

flash_point_c

144 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)

Regulatory Information

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Christoph Böttcher et al.
Analytical chemistry, 79(4), 1507-1513 (2007-02-15)
The coupling of liquid chromatography to electrospray ionization quadrupole time-of-flight mass spectrometry can be a powerful tool for metabolomics, i.e., the comprehensive detection of low molecular weight compounds in biological systems. There have, however, been doubts about the feasibility and
M Gil et al.
Biodegradation, 11(1), 49-53 (2001-02-24)
Aromatic carboxylic acids substituted with methoxylated groups are among the most abundant products in "alpechin", the wastes resulting from pressing olives to obtain olive oil. Degradation of o-methoxybenzoate by an stable consortium made of a gram positive bacterium, Arthrobacter oxydans
Chun-Juan Dong et al.
Planta, 240(4), 687-700 (2014-07-19)
Salicylic acid (SA) is an important plant hormone, and its exogenous application can induce tolerance to multiple environmental stresses in plants. In this study, we examine the potential involvement of endogenous SA in response to chilling in cucumber (Cucumis sativus