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Key Documents

Altri documenti

169978

Sigma-Aldrich

2-Methoxybenzoic acid

ReagentPlus®, 99%

Sinonimo/i:

O-Methylsalicylic acid, o-Anisic acid

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About This Item

Formula condensata:
CH3OC6H4CO2H
Numero CAS:
579-75-9
Peso molecolare:
152.15
Beilstein:
509929
Numero CE:
209-447-8
Numero MDL:
MFCD00002431
Codice UNSPSC:
12352100
ID PubChem:
24850281
NACRES:
NA.22

Livello qualitativo

100

Nome Commerciale

ReagentPlus®

Saggio

99%

Forma fisica

powder

Punto di fusione

98-100 °C (lit.)

Stringa SMILE

COc1ccccc1C(O)=O

InChI

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

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Categorie correlate

Descrizione generale

2-Methoxybenzoic acid was added as carbon supplement in the culture medium of Moraxella osloensis. Photophysics of 2-methoxybenzoic acid has been investigated using both the time-correlated single photon counting and the fluorescence up-conversion techniques.

Applicazioni

2-Methoxybenzoic acid was used as internal standard during quantification of free and conjugated salicylic acid in tomato (Lycopersicon esculentum) cells by HPLC. It was also employed in the synthesis of pthalides.

Note legali

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

Codice della classe di stoccaggio

11 - Combustible Solids

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

291.2 °F - closed cup

Punto d’infiammabilità (°C)

144 °C - closed cup

Dispositivi di protezione individuale

Eyeshields, Gloves, type N95 (US)

Certificati d'analisi (COA)

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Sigma-Aldrich

P7251

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Methyl 2-methoxybenzoate 99%

Sigma-Aldrich

259659

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Benzoic acid ACS reagent, ≥99.5%

Sigma-Aldrich

242381

Benzoic acid

Heterocycles, 39, 47-47 (1994)
Involvement of endogenous salicylic acid content, lipoxygenase and antioxidant enzyme activities in the response of tomato cell suspension cultures to NaCl.
Molina A, et al.
The New phytologist, 156(3), 409-415 (2002)
The photophysics of salicylic acid derivatives in aqueous solution.
Pozdnyakov IP, et al.
Journal of the Physical Society of Japan, 22(5), 449-454 (2009)
R L Crawford et al.
Journal of bacteriology, 121(3), 794-799 (1975-03-01)
Gentisate:oxygen 1,2-oxidoreductase (decyclizing) (EC 1.13.11.4; gentisate 1,2-dioxygenase) from Moraxella osloensis was purified to homogeneity as shown by polyacrylamide gel electrophoresis. The enzyme has a molecular weight of about 154,000 and gives rise to subunits of molecular weight 40,000 in the
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
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