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H55405
4′-Hydroxypropiophenon
98%
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About This Item
Lineare Formel:
HOC6H4COC2H5
CAS-Nummer:
Molekulargewicht:
150.17
Beilstein:
907511
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
PubChem Substanz-ID:
NACRES:
NA.22
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Qualitätsniveau
Assay
98%
mp (Schmelzpunkt)
147.5-148.5 °C (lit.)
SMILES String
CCC(=O)c1ccc(O)cc1
InChI
1S/C9H10O2/c1-2-9(11)7-3-5-8(10)6-4-7/h3-6,10H,2H2,1H3
InChIKey
RARSHUDCJQSEFJ-UHFFFAOYSA-N
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Lagerklassenschlüssel
11 - Combustible Solids
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WGK 3
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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)
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
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
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
R Cizmáriková et al.
Ceska a Slovenska farmacie : casopis Ceske farmaceuticke spolecnosti a Slovenske farmaceuticke spolecnosti, 43(5), 226-228 (1994-10-01)
The present paper carries out the pharmacological evaluation of 4-(2-hydroxy-3-isopropylaminopropoxy)-3-(alkoxymethyl) propiophenones with an ethoxy, propoxy and butoxy-group, whose structures are typical of the blockers of beta-adrenergic receptors. In the above-mentioned compounds the anticalcium effect on the frequency and the amplitude
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