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
Assay:
99%
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
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-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。 。
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 。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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flash_point_f
365.0 °F - closed cup
flash_point_c
185 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
存储类别
11 - Combustible Solids
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)
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)
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 117390-5G | 04061838705051 |
| 117390-100G | 04061838705044 |