Reaxys
PubChem
eMolecules
Reactions (21)
Substances (1)
Citations (19)
Structure
Structure/Compound Data Chemical Name: 3-oxo-2-phenylbutanamide Reaxys Registry Number: 2691802
CAS Registry Number: 4433-77-6 Type of Substance: isocyclic Molecular Formula: C10H11NO2
Linear Structure Formula: C10H11NO2
Molecular Weight: 177.203 InChI Key: FBISRXJSJBLOHX-UHFFFAOYSA-N
1
N° of preparations All Preps | All Reactions
Available Data
N° of ref.
7 prep out of 21 reactions.
Identification Physical Data (6) Spectra (3)
19
Synthesize | Hide Details Find similar Chemical Names and Synonyms 3-oxo-2-phenylbutanamide, 2-phenyl-acetoacetic acid amide, 2-Phenyl-acetessigsaeure-amid, 2-Phenyl-acetoacetamid, α-Phenylacetessigsaeureamid, α-Acetyl-phenylacetamid, α-Phenylacetoacetamid Identification Substance Label (4) Label
Reference
2s
Gotor, Vicente; Liz, Ramon; Testera, Ana Ma
Tetrahedron, 2004 , vol. 60, # 3 p. 607 - 618 Title/Abstract Full Text View citing articles Show Details
2a
Colau,R.; Viel,C.
Bulletin de la Societe Chimique de France, 1979 , vol. <II>, p. 362 - 365 Full Text View citing articles Show Details
Ex7
Tecnifax Corp.
Patent: US3558318 , 1971 ; Chem.Abstr., vol. 74, # 88683 Full Text Show Details
von Z.276
Wolfe et al.
Journal of Organic Chemistry, 1965 , vol. 30, p. 55,57 Full Text Show Details
Related Structure (3) Related Structure
Referenced Compound
Reference
The tautomers given are discussed.
(Z)-3-Hydroxy-2-phenyl-but-2enoic acid amide
Gotor, Vicente; Liz, Ramon; Testera, Ana Ma
Tetrahedron, 2004 , vol. 60, # 3 p. 607 - 618 Title/Abstract Full Text View citing articles Show Details
unter dieser Konstitution beschriebene Verbindung (F: 177-178grad) ist als 2.3-Epoxy-2phenyl-buttersaeure-amid zu formulieren.
Murray; Cloke
Journal of the American Chemical Society, 1934 , vol. 56, p. 2749 Full Text View citing articles Show Details
Knowles; Cloke
Rensselaer polytech. Inst. Bl., 1934 , # 49 p. 1,5, 20 Full Text Show Details
Eine von.
Knowles; Cloke
Journal of the American Chemical Society, 1932 , vol. 54, p. 2028,2036 Full Text Show Details
Physical Data Melting Point (6) Melting Point
Solvent (Melting Point)
Reference
178 °C
ethanol
Colau,R.; Viel,C.
Bulletin de la Societe Chimique de France, 1979 , vol. <II>, p. 362 - 365 Full Text View citing articles Show Details
79 - 85 °C
Tecnifax Corp.
Patent: US3558318 , 1971 ; Chem.Abstr., vol. 74, # 88683 Full Text Show Details
130 °C
Barbieri,W. et al.
Tetrahedron, 1967 , vol. 23, p. 4409 - 4417 Full Text View citing articles Show Details
130 - 131 °C
ethanol
Chatterjea; Prasad
Chemische Berichte, 1960 , vol. 93, p. 1740,1743 Full Text Show Details
131 °C
ethanol
Schreiber
Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1945 , vol. 220, p. 200 Annales de Chimie (Cachan, France), 1947 , vol. <12> 2, p. 84,120 Full Text Show Details
Ogata; Ito
Yakugaku Zasshi, 1916 , # 409 p. 209 Chem.Abstr., 1916 , p. 1646 Full Text Show Details
129 - 130 °C
benzene
Hromatka
Chemische Berichte, 1942 , vol. 75, p. 814,819 Full Text Show Details
Spectra NMR Spectroscopy (2) Description (NMR Spectroscopy)
Nucleus (NMR Spectroscopy)
Solvents (NMR Spectroscopy)
Frequency (NMR Spectroscopy)
Reference
Chemical shifts
1H
CDCl3
200.13 MHz
Gotor, Vicente; Liz, Ramon; Testera, Ana Ma
Tetrahedron, 2004 , vol. 60, # 3 p. 607 - 618 Title/Abstract Full Text View citing articles Show Details
Chemical shifts
13C
CDCl3
50.3 MHz
Gotor, Vicente; Liz, Ramon; Testera, Ana Ma
Tetrahedron, 2004 , vol. 60, # 3 p. 607 - 618 Title/Abstract Full Text View citing articles Show Details
Mass Spectrometry (1) Description (Mass Spectrometry)
Reference
spectrum
Gotor, Vicente; Liz, Ramon; Testera, Ana Ma
Tetrahedron, 2004 , vol. 60, # 3 p. 607 - 618 Title/Abstract Full Text View citing articles Show Details