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Merck

112933

Sigma-Aldrich

Acetanilid

99%

Synonym(e):

N-Phenylacetamid, Essigsäure-anilid

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About This Item

Lineare Formel:
CH3CONHC6H5
CAS-Nummer:
Molekulargewicht:
135.16
Beilstein:
606468
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12352100
eCl@ss:
39031308
PubChem Substanz-ID:
NACRES:
NA.22

Dampfdichte

4.65 (vs air)

Qualitätsniveau

Dampfdruck

1 mmHg ( 114 °C)

Assay

99%

Form

solid

Selbstzündungstemp.

1004 °F

bp

304 °C (lit.)

mp (Schmelzpunkt)

113-115 °C (lit.)

SMILES String

CC(=O)Nc1ccccc1

InChI

1S/C8H9NO/c1-7(10)9-8-5-3-2-4-6-8/h2-6H,1H3,(H,9,10)

InChIKey

FZERHIULMFGESH-UHFFFAOYSA-N

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Allgemeine Beschreibung

Acetanilide undergoes palladium-catalyzed cross-coupling reaction to form ortho-acylacetanilide.

Anwendung

Acetanilide is used as a EOF (electroosmotic flow) marker in the studies of affinity capillary electrophoresis for drug–protein binding.

Piktogramme

Exclamation mark

Signalwort

Warning

H-Sätze

Gefahreneinstufungen

Acute Tox. 4 Oral

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 1

Flammpunkt (°F)

321.8 °F - closed cup

Flammpunkt (°C)

161 °C - closed cup

Persönliche Schutzausrüstung

dust mask type N95 (US), Eyeshields, Gloves


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Deia El-Hady et al.
Journal of pharmaceutical and biomedical analysis, 52(2), 232-241 (2010-01-19)
In order to achieve excellent precision in the estimation of binding constants by affinity capillary electrophoresis (ACE), electroosmotic flow (EOF) stability is the key parameter, especially when using proteins in binding assays. Appropriate rinsing protocols are mandatory. In our study
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Chemical communications (Cambridge, England), 49(7), 689-691 (2012-12-12)
A palladium-catalyzed cascade cross-coupling of acetanilide and toluene for the synthesis of ortho-acylacetanilide is described. Toluene derivatives can act as effective acyl precursors (upon sp(3)-C-H bond oxidation by a Pd/TBHP system) in the oxidative coupling between two C-H bonds. This
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