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688789

Sigma-Aldrich

Acetoacetamide

Arxada quality, 98.5-100.3 % (w/w) (T)

Synonym(s):

α-Acetylacetamide, 3-Oxobutanamide

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About This Item

Linear Formula:
CH3COCH2CONH2
CAS Number:
Molecular Weight:
101.10
Beilstein:
1560550
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

form

crystals

quality

Arxada quality

manufacturer/tradename

Arxada AG

concentration

98.5-100.3 % (w/w) (T)

color

white to yellowish

mp

52.0-54.0 °C
53-56 °C (lit.)

SMILES string

CC(=O)CC(N)=O

InChI

1S/C4H7NO2/c1-3(6)2-4(5)7/h2H2,1H3,(H2,5,7)

InChI key

GCPWJFKTWGFEHH-UHFFFAOYSA-N

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Application

Acetoacetamide is a β-keto amide commonly used in building heterocyclic systems. It can be used in synthesizing various N-substituted acetoacetamides, that are primary precursors for several organic dyes and pigments.

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Chemoselective Amination of ?-Keto Amides.
Hirai S, et al.
Current Organic Chemistry, 20(27), 2911-2916 (2016)
Synthesis and structure of new 1,2,3-triazolyl substituted 1,3,5-triazines.
Mikhaylichenko S, et al.
European Journal of Chemistry, 3(1), 1-9 (2012)
Synthesis and evaluation of 1, 2, 4-triazolo [1, 5-a] pyrimidines as antibacterial agents against Enterococcus faecium.
Wang H, et al.
Journal of Medicinal Chemistry, 58(10), 4194-4203 (2015)
Three?Component Synthesis of Pyrrole?Related Nitrogen Heterocycles by a Hantzsch?Type Process: Comparison between Conventional and High?Speed Vibration Milling Conditions.
Estevez V, et al.
Asian Journal of Organic Chemistry, 5(5), 652-662 (2016)
A Simple and Efficient Regioselective and Chemoselective Synthesis of New Substituted 3?Methyl?6?arylpyridazine?4?carboxamides and 5?Oxo?3?aryl?5,6?dihydropyrido [4, 3?c] pyridazine?8?carbaldehydes.
Lotfata A, et al.
Journal of Heterocyclic Chemistry, 55(3), 603-609 (2018)

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