登录 查看组织和合同定价。
选择尺寸
关于此项目
线性分子式:
CH3OC6H4CO2H
化学文摘社编号:
分子量:
152.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
209-574-9
Beilstein/REAXYS Number:
508838
MDL number:
Assay:
99%
mp
105-107 °C (lit.)
solubility
95% ethanol: soluble 50 mg/mL, clear, colorless to faintly yellow
functional group
carboxylic acid
InChI key
XHQZJYCNDZAGLW-UHFFFAOYSA-N
InChI
1S/C8H8O3/c1-11-7-4-2-3-6(5-7)8(9)10/h2-5H,1H3,(H,9,10)
SMILES string
COc1cccc(c1)C(O)=O
product line
ReagentPlus®
assay
99%
bp
170-172 °C/10 mmHg (lit.)
Quality Level
General description
3-甲氧基苯甲酸是天然产物合成中的重要中间体。
Application
3-甲氧基苯甲酸用于合成和表征铕(III)和钆(III)的 3-甲氧基苯甲酸酯。将其用于将芳族羧酸转化为甲酯并使用硼氢化钠-THF-甲醇系统还原成相应的伯醇。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
法规信息
新产品
此项目有
Synthesis, characterization and thermal behaviour of solid-state compounds of europium (III) and gadolinium (III) 3-methoxybenzoate.
Dametto PR, et al.
Journal of Thermal Analysis and Calorimetry, 97(2), 765-768 (2009)
Sodium borohydride reduction of aromatic carboxylic acids via methyl esters.
Saeed A and Ashraf Z.
Journal of Chemical Sciences (Bangalore), 118(5), 419-423 (2006)
A S Waldman et al.
Nucleic acids research, 19(21), 5943-5947 (1991-11-11)
We determined the effect of 3-methoxybenzamide (3-MB), a competitive inhibitor of poly(ADP-ribose) polymerase (E.C. 2.4.2.30), on intrachromosomal homologous recombination in mouse Ltk- cells. We used a cell line that contained in its genome two defective Herpes thymidine kinase (tk) genes
D H Lee et al.
Xenobiotica; the fate of foreign compounds in biological systems, 29(9), 909-916 (1999-11-05)
1. 2-(Allylthio)pyrazine (2-AP) has been demonstrated to protect the liver against toxicants by inhibiting CYP2E1 activity. Since 2-mercaptopyrazine (2-MP) is presumed to be a metabolite of 2-AP, the experiments were performed to determine whether rat liver microsomal and/or cytosolic preparations
Ljerka Lah et al.
Molecular microbiology, 81(5), 1374-1389 (2011-08-04)
Cytochromes P450 (CYPs) catalyse diverse reactions and are key enzymes in fungal primary and secondary metabolism, and xenobiotic detoxification. CYP enzymatic properties and substrate specificity determine the reaction outcome. However, CYP-mediated reactions may also be influenced by their redox partners.
我们的科学家团队拥有各种研究领域经验,包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持