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Merck
CN

H55405

4′-Hydroxypropiophenone

98%

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About This Item

Linear Formula:
HOC6H4COC2H5
CAS Number:
Molecular Weight:
150.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-743-2
Beilstein/REAXYS Number:
907511
MDL number:
Assay:
98%
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assay

98%

InChI

1S/C9H10O2/c1-2-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3

InChI key

RARSHUDCJQSEFJ-UHFFFAOYSA-N

SMILES string

CCC(=O)c1ccc(O)cc1

mp

147.5-148.5 °C (lit.)

Quality Level

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Storage Class

11 - Combustible Solids

wgk

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves


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R Cizmáriková et al.
Ceskoslovenska farmacie, 42(2), 82-85 (1993-04-01)
Within the relationship of the structure and effect of new beta-adrenolytic agents derivatived from p-hydroxyacetophenone and p-hydroxypropiophenone with a propoxymethyl group in the lipophilic part of the molecule and with a propanamine, a butanamine and a pyrrolidine in the side-chain
Zack E Bryant et al.
Bioorganic & medicinal chemistry letters, 21(3), 912-915 (2011-01-14)
A series of ethacrynic acid analogues, lacking the α,β-unsaturated carbonyl unit, was synthesized and subsequently evaluated for their ability to inhibit the migration of human breast cancer cells, Hs578Ts(i)8 as well as of human prostate cancer cells, C4-2B. These cell
p-Hydroxypropiophenone effects on azo dye-induced alterations in mouse hepatic cells: light and electron microscopic study.
N J Unakar
Journal of the National Cancer Institute, 44(4), 873-891 (1970-04-01)
Morio Yoshimura et al.
Chemical & pharmaceutical bulletin, 65(9), 878-882 (2017-09-05)
Mousouchiku extract is prepared from the bamboo-sheath of Phyllostachys heterocycla MITF. (Poaceae), and is registered as a food manufacturing agent in the List of Existing Food Additives in Japan. This study describes the chromatographic evaluation of characteristic components of this
A Tanner et al.
Journal of bacteriology, 182(23), 6565-6569 (2000-11-14)
An arylketone monooxygenase was purified from Pseudomonas putida JD1 by ion exchange and affinity chromatography. It had the characteristics of a Baeyer-Villiger-type monooxygenase and converted its substrate, 4-hydroxyacetophenone, into 4-hydroxyphenyl acetate with the consumption of one molecule of oxygen and

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