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:
InChI key
ILUJQPXNXACGAN-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5H,1H3,(H,9,10)
SMILES string
COc1ccccc1C(O)=O
biological source
synthetic
assay
≥99%
mp
98-100 °C (lit.)
application(s)
flavors and fragrances
Quality Level
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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T Sasaki et al.
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine, 50(5), 905-909 (1999-04-24)
For in vivo measurement of the hydroxyl radical (.OH), we synthesized [11C]salicylic acid, [11C]O-acetylsalicylic acid and [11C]2-methoxybenzoic acid by carboxylation of 2-bromomagnesiumanisol using [11C]CO2. The radiochemical yield of [11C]salicylic acid, [11C]O-acetylsalicylic acid and [11C]2-methoxybenzoic acid calculated from trapped [11C]CO2 in
Quan Zhou et al.
The Journal of organic chemistry, 73(20), 8049-8056 (2008-09-20)
Mander reductive alkylation of methyl 2-methoxybenzoate with prenyl bromide and hydrolysis of the enol ether afforded methyl 6-oxo-1-prenyl-2-cyclohexenecarboxylate. This was converted in five steps (reduction of the ketone, saponification, iodolactonization, ozonolysis, and intramolecular aldol reaction) to a spiro lactone cyclopentenal.
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
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
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
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