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Merck
모든 사진(1)

주요 문서

W394300

Sigma-Aldrich

o-Anisic acid

≥99%

동의어(들):

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
Beilstein:
509929
EC Number:
MDL number:
UNSPSC 코드:
12164502
PubChem Substance ID:

생물학적 소스

synthetic

Quality Level

분석

≥99%

mp

98-100 °C (lit.)

응용 분야

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

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호환 제품

제품 번호
설명
가격

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point (°F)

291.2 °F - closed cup

Flash Point (°C)

144 °C - closed cup

개인 보호 장비

Eyeshields, Gloves, type N95 (US)


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문서 라이브러리 방문

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
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.
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
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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