M18655
4-甲氧基苯酚
ReagentPlus®, 99%
别名:
对甲氧基苯酚, 4-MP, HQMME, MEHQ, 对愈创木酚, 对羟基苯甲醚, 氢醌单甲醚
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关于此项目
线性分子式:
CH3OC6H4OH
化学文摘社编号:
分子量:
124.14
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-769-8
Beilstein/REAXYS Number:
507924
MDL number:
Assay:
99%
vapor density
4.3 (vs air)
Quality Level
vapor pressure
<0.01 mmHg ( 20 °C)
product line
ReagentPlus®
assay
99%
autoignition temp.
789 °F
bp
243 °C (lit.)
mp
55-57 °C (lit.)
SMILES string
COc1ccc(O)cc1
InChI
1S/C7H8O2/c1-9-7-4-2-6(8)3-5-7/h2-5,8H,1H3
InChI key
NWVVVBRKAWDGAB-UHFFFAOYSA-N
Gene Information
human ... TYR(7299)
Application
4-甲氧基苯酚可用于通过甲基叔丁基醚在非沸石固体酸性催化剂上进行甲基烷基化，以合成丁基化羟基茴香醚。与Friedel-Crafts烷基化反应相比，该方法更加环保。根据反应条件，4-MP也可以与亚硝酸水溶液发生反应，并以不同的比例形成2-硝基-4-甲氧基苯酚和苯醌。4-Mp可用作设计β-环糊精4-甲氧基苯酚缀合物的合成砌块，其可作为药物络合的潜在配体。
Legal Information
ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany
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signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Aquatic Chronic 3 - Eye Irrit. 2 - Skin Sens. 1
存储类别
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
Intermolecular interactions between doxorubicin and ?-cyclodextrin 4-methoxyphenol conjugates
Swiech O
The Journal of Physical Chemistry B, 116(6), 1765-1771 (2012)
Nitration and oxidation of 4-methoxyphenol by nitrous acid in aqueous acid solution.
Beake B D
J. Chem. Soc. Perkin Trans. II, (2), 335-340 (1994)
James R Allen et al.
Genetics, 213(2), 555-566 (2019-08-25)
In larval zebrafish, melanocyte stem cells (MSCs) are quiescent, but can be recruited to regenerate the larval pigment pattern following melanocyte ablation. Through pharmacological experiments, we found that inhibition of γ-aminobutyric acid (GABA)-A receptor function, specifically the GABA-A ρ subtype
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| M18655-500G | 04061834041191 |
| M18655-50LB | 04061832885964 |
| M18655-5G | 04061834041207 |
| M18655-100G | 04061835559510 |
| M18655-1KG | 04061834041184 |