169978
2-甲氧基苯甲酸
ReagentPlus®, 99%
别名:
O-甲基水杨酸, 邻茴香酸
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线性分子式:
CH3OC6H4CO2H
化学文摘社编号:
分子量:
152.15
Beilstein:
509929
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
质量水平
产品线
ReagentPlus®
方案
99%
表单
powder
mp
98-100 °C (lit.)
官能团
carboxylic acid
SMILES字符串
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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一般描述
2-甲氧基苯甲酸在奥斯陆莫拉菌培养基中可作为碳补充剂进行添加 。使用时间相关的单光子计数和荧光上转换技术已对2-甲氧基苯甲酸的光物理学进行了研究。
应用
在通过HPLC对番茄（Lycopersicon esculentum）细胞中游离和共轭水杨酸进行定量的过程中，使用2-甲氧基苯甲酸作为内标进行测定。它也可用于合成苯酞。
法律信息
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
储存分类代码
11 - Combustible Solids
WGK
WGK 3
闪点(°F)
291.2 °F - closed cup
闪点(°C)
144 °C - closed cup
个人防护装备
Eyeshields, Gloves, type N95 (US)
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)
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
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