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A21401

Sigma-Aldrich

4-Acetylpyridin

97%

Synonym(e):

Methyl-4-pyridylketon

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About This Item

Empirische Formel (Hill-System):
C7H7NO
CAS-Nummer:
1122-54-9
Molekulargewicht:
121.14
Beilstein:
107629
EG-Nummer:
214-350-9
MDL-Nummer:
MFCD00006433
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24890629
NACRES:
NA.22

Assay

97%

Form

liquid

Brechungsindex

n20/D 1.529 (lit.)

SMILES String

CC(=O)c1ccncc1

InChI

1S/C7H7NO/c1-6(9)7-2-4-8-5-3-7/h2-5H,1H3

InChIKey

WMQUKDQWMMOHSA-UHFFFAOYSA-N

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Verwandte Kategorien

Piktogramme

Exclamation mark
GHS07

Signalwort

Warning

H-Sätze

H315

Gefahreneinstufungen

Skin Irrit. 2

Lagerklassenschlüssel

10 - Combustible liquids

WGK

WGK 3

Flammpunkt (°F)

219.2 °F - closed cup

Flammpunkt (°C)

104 °C - closed cup

Persönliche Schutzausrüstung

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Y Imamura et al.
Journal of biochemistry, 125(1), 41-47 (1999-01-09)
An enzyme responsible for the ketone-reduction of 4-benzoylpyridine (4BP) was purified 350-fold to homogeneity from the cytosolic fraction of rabbit heart. The purified enzyme exhibited a molecular mass of 110 kDa on gel filtration, and 27 kDa on SDS-PAGE, indicating
A Topacli et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 57(7), 1385-1391 (2001-07-12)
The normal coordinate analysis has been performed for 4-aminopyridine (4-apy) assuming C2v molecular symmetry. A Urey-Bradley force field has been used. The force constants are adjusted to fit the observed frequencies for 4-apy and its deuterated species. The vibrational assignment
Y Imamura et al.
Biochemistry and molecular biology international, 33(5), 893-899 (1994-08-01)
A correlation was observed between the values of specificity constant (kcat/Km) of carbonyl reductase from rabbit liver for acetohexamide analogs and their partition coefficients. This result indicates that the hydrophobicity in straight-chain alkyl groups of acetohexamide analogs plays an important
S G Zhu et al.
Brain research, 481(2), 356-360 (1989-03-06)
Measurements of striatal choline acetyltransferase (ChAT) and glutamic acid decarboxylase (GAD) activities indicated that systemic administration of 4-8 mg/kg of MK-801 to rats completely blocked neuronal damage due to intrastriatal injections of 75-150 nmol of quinolinic acid. Similar experiments with
A Hall et al.
Neuroscience letters, 85(1), 110-112 (1988-02-15)
4-Acetylpyridine, earlier reported by us to be an anticonvulsant, offers long-lasting protection after a single administration against hypothermic restraint stress-induced gastric ulceration in mice. Electroshock convulsions, marginally but not significantly protective against such ulcers themselves, when coupled with 4-acetylpyridine administration
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