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H55405

Sigma-Aldrich

4′-Hydroxypropiophenone

98%

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Linear Formula:
HOC6H4COC2H5
CAS Number:
70-70-2
Molecular Weight:
150.17
Beilstein:
907511
EC Number:
200-743-2
MDL number:
MFCD00002361
PubChem Substance ID:
24895701
NACRES:
NA.22

Quality Level

100

Assay

98%

mp

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

InChI key

RARSHUDCJQSEFJ-UHFFFAOYSA-N

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1 of 4

This Item
H9904137235T68101
4′-Hydroxypropiophenone 98%

Sigma-Aldrich

H55405

4′-Hydroxypropiophenone

2′-Hydroxy-4′,5′-dimethoxyacetophenone ≥98%

Sigma-Aldrich

H9904

2′-Hydroxy-4′,5′-dimethoxyacetophenone

3′,4′-Dimethylacetophenone 98%

Sigma-Aldrich

137235

3′,4′-Dimethylacetophenone

3′,4′,5′-Trimethoxyacetophenone 98%

Sigma-Aldrich

T68101

3′,4′,5′-Trimethoxyacetophenone

mp

147.5-148.5 °C (lit.)

mp

-

mp

-

mp

78-80 °C (lit.)

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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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
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
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, 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
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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