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Merck
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重要文件

224502

Sigma-Aldrich

4-羟基苯乙酸甲酯

ReagentPlus®, 99%

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About This Item

線性公式:
HOC6H4CH2CO2CH3
CAS號碼:
分子量::
166.17
Beilstein:
2087538
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

solid

bp

162-163 °C/5 mmHg (lit.)

mp

55-58 °C (lit.)

官能基

ester

SMILES 字串

COC(=O)Cc1ccc(O)cc1

InChI

1S/C9H10O3/c1-12-9(11)6-7-2-4-8(10)5-3-7/h2-5,10H,6H2,1H3

InChI 密鑰

XGDZEDRBLVIUMX-UHFFFAOYSA-N

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一般說明

Methyl 4-hydroxyphenylacetate inhibits the activity of tobacco mosaic virus (TMV).

應用

Methyl 4-hydroxyphenylacetate was used in the synthesis of 4-(2-hydroxy-3-isopropylamino)propoxyphenylacetic acid.

法律資訊

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

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象形圖

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訊號詞

Warning

危險聲明

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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分析證明 (COA)

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S H Jung et al.
Archives of pharmacal research, 23(3), 226-229 (2000-07-15)
To obtain the standard compounds of metoprolol for a pharmacokinetic study, a convenient synthetic procedure to prepare enantiomers of metoprolol (3a) and its major metabolites, 2-4-(2-hydroxy-3-isopropylamino)propoxyphenylethanol (3b) and 4-(2-hydroxy-3-isopropylamino)propoxyphenylacetic acid (4), was developed from their respective starting materials, 4-(2-methoxyethyl)phenol (1a)
Shuo Shen et al.
Natural product research, 27(24), 2286-2291 (2013-08-22)
A new compound 2-(4-hydroxybenzoyl) quinazolin-4(3H)-one (1) and four known compounds were isolated from a marine fungus Penicillium oxalicum 0312F1. The structure of the new compound 1 was elucidated based on the spectroscopic analysis. Bioactivity assays showed that 2-(4-hydroxybenzyl) quinazolin-4(3H)-one (2)

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