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W517607

Sigma-Aldrich

Acetoacetanilide

≥98%

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About This Item

Linear Formula:
CH3COCH2CONHC6H5
CAS Number:
102-01-2
Molecular Weight:
177.20
Beilstein/REAXYS Number:
473419
EC Number:
202-996-4
MDL number:
MFCD00008780
UNSPSC Code:
12164502
PubChem Substance ID:
24901924

biological source

synthetic

vapor density

6.1 (vs air)

assay

≥98%

autoignition temp.

843 °F

mp

83-88 °C (lit.)

application(s)

flavors and fragrances

organoleptic

faint

SMILES string

CC(=O)CC(=O)Nc1ccccc1

InChI

1S/C10H11NO2/c1-8(12)7-10(13)11-9-5-3-2-4-6-9/h2-6H,7H2,1H3,(H,11,13)

InChI key

DYRDKSSFIWVSNM-UHFFFAOYSA-N

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Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
17130KO
10404DA
06223CO
03330PU

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Syntheses of 1,3-imidazolin-2-ones and 1,3-imidazolin-2-thiones from new building blocks, gamma-aminoacetoacetanilides.
Jong Tak Lee et al.
Journal of combinatorial chemistry, 10(6), 803-806 (2008-09-27)
Thin-layer chromatographic separation of some sulpha drugs using acetoacetanilide as a coupling agent.
R Jain et al.
Journal of chromatography, 441(2), 454-457 (1988-06-10)
Yinqiao Hu et al.
Chemical communications (Cambridge, England), 48(5), 690-692 (2011-12-03)
The regiospecific β-lactam ring-opening/recyclization reaction of N-aryl-3-spirocyclic-β-lactams, made by the one-pot cyclization reaction of acetoacetanilides, has been achieved for the first time using a Lewis-Brønsted acids combined superacid catalyst system, thus providing an efficient entry to 3-spirocyclicquinolin-4(1H)-ones. A mechanism involving
Zhimin Chen et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 68(3), 918-926 (2007-02-20)
A new chelating ligand, 2-(2-(5-tert-butylisoxazol-3-yl)hydrazono)-N-(2,4-dimethylphenyl)-3-oxobutanamide (HL), and its four binuclear transition metal complexes, M(2)(L)(2) (micro-OCH(3))(2) [M=Ni(II), Co(II), Cu(II), Zn(II)], were synthesized using the procedure of diazotization, coupling and metallization. Their structures were postulated based on elemental analysis, (1)H NMR, MALDI-MS
N Vijayan et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 93, 75-80 (2012-04-03)
Single crystals of acetoacetanilide have been successfully grown by slow evaporation solution growth method at room temperature. The grown crystal belongs to orthorhombic crystal system having the lattice dimensions of a=8.686Å, b=11.104Å, c=19.232Å. Its crystalline perfection was examined by home-made
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