117390
4-Methoxybenzoic acid
ReagentPlus®, 99%
Sinónimos:
p-Anisic acid, 4-Methoxybenzoic acid, p-Methoxybenzoic acid, Draconic acid
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Fórmula lineal:
CH3OC6H4CO2H
Número CAS:
Peso molecular:
152.15
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39023905
UNSPSC Code:
12352100
EC Number:
202-818-5
MDL number:
Beilstein/REAXYS Number:
508910
Assay:
99%
Servicio técnico
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Permítanos ayudarleproduct line
ReagentPlus®
assay
99%
mp
182-185 °C (lit.)
solubility
H2O: soluble 2500 parts, alcohol: freely soluble, boiling water: soluble, chloroform: freely soluble, diethyl ether: freely soluble, ethyl acetate: freely soluble
functional group
carboxylic acid
SMILES string
COc1ccc(cc1)C(O)=O
InChI
1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10)
InChI key
ZEYHEAKUIGZSGI-UHFFFAOYSA-N
General description
4-Methoxybenzoic acid is the sole source of carbon and energy for growth in the cultures of Nocardia sp. DSM 1069.
Application
4-Methoxybenzoic acid was used in oxidation and reduction of cytochrome c in solution through different self-assembled monolayers on gold electrodes using cyclic voltammetry.
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
flash_point_f
365.0 °F - closed cup
flash_point_c
185 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
Clase de almacenamiento
11 - Combustible Solids
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Control of the electron transfer rate between cytochrome c and gold electrodes by the manipulation of the electrode's hydrogen bonding character.
Liu H, et al.
Langmuir, 19(6), 2378-2387 (2003)
Degradation of coniferyl alcohol and other lignin-related aromatic compounds by Nocardia sp. DSM 1069.
Eggeling L and Sahm H.
Archives of Microbiology, 126(2), 141-148 (1980)
M Wessels et al.
Journal of natural products, 64(12), 1556-1558 (2002-01-05)
From the hydrophilic extract of the ascidian Polycarpa aurata three new compounds, N-(4-methoxybenzoyl)-N'-methylguanidine (1), butyl 2-(4-methoxyphenyl)-2-oxoacetate (2), and 2-(4-methoxyphenyl)-N-methyl-2-oxoacetamide (3), together with the known compounds methyl 2-(4-methoxyphenyl)-2-oxoacetate (4) and 4-methoxybenzoic acid were isolated. The structures of all isolates were determined