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%
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.
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
R Cizmáriková et al.
Ceskoslovenska farmacie, 39(9), 403-408 (1990-11-01)
Within the framework of the study of the structure-effect relationship, a series of novel potential beta-adrenolytic agents derived from p-hydroxyacetophenone and p-hydroxypropiophenone with an alyloxymethyl and a cycloalkyloxymethyl group in the lipophilic part of the molecule and an isopropyl and
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
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)
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