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ChemicalBook--->CAS DataBase List--->39562-25-9

39562-25-9

39562-25-9 Structure

39562-25-9 Structure
IdentificationBack Directory
[Name]

Isopropyl 2-(3-nitrobenzylidene)acetoacetate
[CAS]

39562-25-9
[Synonyms]

Nilvadipine Impurity L
Azelnidipine Impurity 5
2-(3-nitrobenzylidene)acetoacetate
isopropyl 2-(3-nitrobenzylidene) acetacetate
Isopropyl-2-(3-Nitrobenzolidene)Acetoacetate
Isopropyl 2-(3-nitrobenzylidene)acetoacetate
Isopropyl 2-3- nitrobcnzylidcnelacetoucctatc
ISOPROPYL 2-(M-NITROBENZYLIDENE)-ACETOACETATE
Isopropyl 2-(3-nitrobenzylidene)-3-oxobutanoate
Isopropyl 2-(3-Nitrobenzylidene) Acetaacetate ?
2- (3- nitro benzylidene) isopropyl acetoacetate
2-(3-NITROBENZYLIDENE)ACETOACETATE/CAS:39562-25-9
α-Acetyl-3-nitrobenzeneacrylic acid isopropyl ester
(E)-ISOPROPYL 2-(3-NITROBENZYLIDENE)-3-OXOBUTANOATE
2-(3-Nitrobenzylidene)acetoacetic acid isopropyl ester
5-Methyl-2-[(3-nitrophenyl)Methylidene]-3-oxohexanoate
2-(3-Nitrobenzylidene)-3-oxobutyric acid isopropyl ester
2-(3-Nitrobenzylidene)-3-oxobutanoic Acid Isopropyl Ester
3-oxo-2-(3-nitrophenylmethylene)butanoic acid isopropyl ester
2-[(3-nitrophenyl)methylidene]-3-oxobutanoic acid propan-2-yl ester
Isopropyl 2-(3-nitrobenzylidene)-3-oxobutanoate (Nimodipine Impurity)
Butanoic acid, 2-[(3-nitrophenyl)methylene]-3-oxo-, 1-methylethyl ester
Isopropyl 2-(3-nitrobenzylidene)acetoacetate (E)-ISOPROPYL 2-(3-NITROBENZYLIDENE)-3-OXOBUTANOATE
[EINECS(EC#)]

609-720-5
[Molecular Formula]

C14H15NO5
[MDL Number]

MFCD01234175
[MOL File]

39562-25-9.mol
[Molecular Weight]

277.27
Chemical PropertiesBack Directory
[Melting point ]

94 °C
[Boiling point ]

404.9±35.0 °C(Predicted)
[density ]

1.229±0.06 g/cm3(Predicted)
[storage temp. ]

2-8°C
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302-H315-H319
[Precautionary statements ]

P261-P305+P351+P338
Hazard InformationBack Directory
[Synthesis]

A preparation method of isopropyl 2-(3-nitrobenzylidene)acetoacetate comprises the following steps: carrying out condensation reaction on 3-nitrobenzaldehyde and isopropyl acetoacetate as initial raw materials by using an organic solvent as a solvent in the presence of catalysts acetic acid and piperidine for 2-8 hours; after carrying out vacuum concentration on the filtrate at 80 ℃ to 2/3-3/4 by volume, cooling to -5-5 ℃ while stirring to crystallize overnight; and filtering, and recrystallizing with isopropanol to finally obtain the isopropyl 2-(3-nitrobenzylidene)acetoacetate.
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