ChemicalBook--->CAS DataBase List--->89532-38-7

89532-38-7

89532-38-7 Structure

89532-38-7 Structure
IdentificationBack Directory
[Name]

2-cyclopropyl-1H-imidazole
[CAS]

89532-38-7
[Synonyms]

2-CyclopropyliMidazole
2-cyclopropyl-1H-imidazole
1H-Imidazole, 2-cyclopropyl-
2-Cyclopropyl-1H-iMidazol...
[Molecular Formula]

C6H8N2
[MDL Number]

MFCD19217297
[MOL File]

89532-38-7.mol
[Molecular Weight]

108.14
Chemical PropertiesBack Directory
[Melting point ]

138-139℃
[Boiling point ]

324.2±11.0 °C(Predicted)
[density ]

1?+-.0.06 g/cm3(Predicted)
[storage temp. ]

Sealed in dry,Room Temperature
[pka]

14.39±0.10(Predicted)
[Appearance]

White to light yellow Solid
Questions And AnswerBack Directory
[Uses]

2-Cyclopropyl-1H-imidazole is a heterocyclic organic compound, mainly used as a pharmaceutical intermediate.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)Corrosion (GHS05)
GHS07,GHS05
[Signal word ]

Danger
[Hazard statements ]

H335-H318-H302-H315
[Precautionary statements ]

P264-P270-P301+P312-P330-P501-P264-P280-P302+P352-P321-P332+P313-P362-P280-P305+P351+P338-P310
Spectrum DetailBack Directory
[Spectrum Detail]

2-cyclopropyl-1H-imidazole(89532-38-7)1HNMR
Hazard InformationBack Directory
[Synthesis]

1,2-Ethenediylbis(oxy) (9CI)

131543-46-9

Cyclopropanecarboxaldehyde

1489-69-6

2-cyclopropyl-1H-imidazole

89532-38-7

A methanol (5 mL) solution of cyclopropanecarboxaldehyde (500 mg, 7.13 mmol) and acetaldehyde (455 mg, 7.84 mmol) was added to a 25 mL round bottom flask. The reaction mixture was cooled to 0 °C, followed by dropwise addition of 25% aqueous ammonium hydroxide solution (1 mL). The resulting mixture was stirred at 0 °C for 3 h, followed by continued stirring at room temperature overnight. Upon completion of the reaction, the mixture was concentrated under reduced pressure and the residue was dissolved in saturated saline (50 mL). The aqueous phase was extracted with ethyl acetate (3 x 10 mL), the organic layers were combined and dried over anhydrous sodium sulfate. After filtration, the filtrate was concentrated under reduced pressure to afford the title compound 2-cyclopropyl-1H-imidazole (600 mg, 78% yield) as a light brown solid.

[References]

[1] Patent: WO2014/8197, 2014, A1. Location in patent: Page/Page column 115
[2] Patent: WO2015/95767, 2015, A1. Location in patent: Page/Page column 130
[3] Patent: US2011/52578, 2011, A1
[4] European Journal of Medicinal Chemistry, 2016, vol. 108, p. 605 - 615
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