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Merck
CN

534595

Sigma-Aldrich

4-(2-甲氧基乙基)苯酚

97%

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线性分子式:
CH3O(CH2)2C6H4OH
CAS号:
分子量:
152.19
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

97%

mp

42-45 °C (lit.)

SMILES字符串

COCCc1ccc(O)cc1

InChI

1S/C9H12O2/c1-11-7-6-8-2-4-9(10)5-3-8/h2-5,10H,6-7H2,1H3

InChI key

FAYGEALAEQKPDI-UHFFFAOYSA-N

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一般描述

甲基乙烯基醚和 4-溴硝基苯反应可制备 4-(2-甲氧基乙基)苯酚。

应用

4-(2-甲氧基乙基)苯酚可用于制备美托洛尔(MAM)的甲基类似物。

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

230.0 °F

闪点(°C)

110 °C

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

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Evidence that serine 304 is not a key ligand-binding residue in the active site of cytochrome P450 2D6.
Ellis SW, et al.
The Biochemical Journal, 345(3), 565-571 (2000)
A New Route to 4-(2-Methoxyethyl) Phenol Via Palladium-Catalysed Arylation of Methyl Vinyl Ether.
Hallberg A, et al.
Synthetic Communications, 15(13), 1131-1136 (1985)
M Allaoua et al.
Journal of applied microbiology, 125(4), 1162-1174 (2018-05-18)
In vitro and in vivo studies were conducted to test a new carvacrol-based product designed to delay the carvacrol release so that it could reach the caeca of broiler chickens in order to control Campylobacter jejuni. Antimicrobial activity of carvacrol, a
Alfred Svan et al.
Journal of mass spectrometry : JMS, 51(3), 207-218 (2016-03-10)
Identification of degradation products from trace organic compounds, which may retain the biological activity of the parent compound, is an important step in understanding the long-term effects of these compounds on the environment. Constructed wetlands have been successfully utilized to

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