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Merck
CN

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
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
227-774-4
Beilstein/REAXYS Number:
1560550
MDL number:
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Product Name

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

InChI key

GCPWJFKTWGFEHH-UHFFFAOYSA-N

InChI

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

SMILES string

CC(=O)CC(N)=O

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.)

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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

11 - Combustible Solids

wgk

WGK 1

flash_point_f

235.4 °F - closed cup

flash_point_c

113 °C - closed cup

ppe

Eyeshields, Gloves, type N95 (US)


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

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