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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:
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

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

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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