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Merck

169978

Sigma-Aldrich

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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About This Item

线性分子式:
CH3OC6H4CO2H
CAS号:
分子量:
152.15
Beilstein:
509929
EC號碼:
MDL號碼:
分類程式碼代碼:
12352100
PubChem物質ID:
NACRES:
NA.22

品質等級

產品線

ReagentPlus®

化驗

99%

形狀

powder

mp

98-100 °C (lit.)

官能基

carboxylic acid

SMILES 字串

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 密鑰

ILUJQPXNXACGAN-UHFFFAOYSA-N

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一般說明

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

應用

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

法律資訊

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

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

291.2 °F - closed cup

閃點(°C)

144 °C - closed cup

個人防護裝備

Eyeshields, Gloves, type N95 (US)


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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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)
Heterocycles, 39, 47-47 (1994)
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)
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
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.

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