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224502

Sigma-Aldrich

Methyl 4-hydroxyphenylacetate

ReagentPlus®, 99%

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About This Item

Linear Formula:
HOC6H4CH2CO2CH3
CAS Number:
14199-15-6
Molecular Weight:
166.17
Beilstein/REAXYS Number:
2087538
EC Number:
238-050-2
MDL number:
MFCD00002387
UNSPSC Code:
12352100
PubChem Substance ID:
24853443
NACRES:
NA.22

product line

ReagentPlus®

assay

99%

form

solid

bp

162-163 °C/5 mmHg (lit.)

mp

55-58 °C (lit.)

SMILES string

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 key

XGDZEDRBLVIUMX-UHFFFAOYSA-N

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General description

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

Application

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

Legal Information

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

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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)
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)

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