688789
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
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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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Colour and constitution relationships in organic pigments. Part 1?Monoazoacetoacetanilides.
Christie RM, et al.
Dyes and Pigments, 9(1), 37-56 (1988)
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)
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)
Chemoselective Amination of ?-Keto Amides.
Hirai S, et al.
Current Organic Chemistry, 20(27), 2911-2916 (2016)
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)
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