117390
4-甲氧基苯甲酸
ReagentPlus®, 99%
别名:
p -茴香酸, 4-甲氧基苯甲酸, 对甲氧基苯甲酸, 龙血酸
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关于此项目
线性分子式:
CH3OC6H4CO2H
化学文摘社编号:
分子量:
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
产品名称
4-甲氧基苯甲酸, ReagentPlus®, 99%
InChI key
ZEYHEAKUIGZSGI-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3,(H,9,10)
SMILES string
COc1ccc(cc1)C(O)=O
product 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
Quality Level
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Application
用循环伏安法研究了 4-甲氧基苯甲酸在金电极上通过不同的自组装膜对溶液中细胞色素 c 的氧化和还原 。
General description
4-甲氧基苯甲酸是诺卡氏菌 sp. DSM 1069 培养物中唯一的碳和能量来源。 。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
13 - Non Combustible Solids
wgk
WGK 1
flash_point_f
365.0 °F - closed cup
flash_point_c
185 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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
A Hage et al.
Applied microbiology and biotechnology, 52(6), 834-838 (2000-01-05)
Ligninolytic basidiomycetes were screened for their ability to reduce aryl acids to the corresponding aldehydes and alcohols. Seven fungal strains converted p-anisic acid in high molar yields to the reduced products. The white-rot fungus Bjerkandera sp. strain BOS55 was one
N Chaves et al.
Journal of chemical ecology, 27(3), 611-621 (2001-07-10)
Eleven allelochemicals (ferulic acid, cinnamic acid, 4-hydroxybenzoic acid, hydroxycinnamic acid, methyl propionate, oxalic acid, methylmalonic acid, p-anisic acid, butyric acid, 3-hydroxybutyric acid, and azulene) were identified in the exudate of Cistus ladanifer L. We studied the effect of each on
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