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Thermo Scientific Chemicals
(4-Imidazolyl)acetonitrile, 97%
CAS: 18502-05-1 | C5H5N3 | 107.116 g/mol
化学物質識別子
CAS18502-05-1
IUPAC Name2-(1H-imidazol-5-yl)acetonitrile
Molecular FormulaC5H5N3
InChI KeyDQZBHUXBFNBJLX-UHFFFAOYSA-N
SMILESN#CCC1=CN=CN1
さらに表示
仕様
スペックシート
スペックシートMelting Point (clear melt)129.5-138.5?C
Appearance (Color)Orange to brown
Assay (GC)≥96.0%
FormPowder
(4-Imidazolyl)acetonitrile is used to produce 2-(1H-imidazol-4-yl)-3-phenyl-acrylonitrile at ambient temperature.
This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.
Applications
(4-Imidazolyl)acetonitrile is used to produce 2-(1H-imidazol-4-yl)-3-phenyl-acrylonitrile at ambient temperature.
Solubility
Insoluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
(4-Imidazolyl)acetonitrile is used to produce 2-(1H-imidazol-4-yl)-3-phenyl-acrylonitrile at ambient temperature.
Solubility
Insoluble in water.
Notes
Keep container tightly sealed. Store in cool, dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only
General References:
- G. A. A. Kivits.; J. Hora. A derivative of (4-imidazolyl)acetaldehyde of proven structure. Recueil des Travaux Chimiques des Pays-Bas. 1975, 94 (11), 245-246.
- N. J. van Hoboken.; P. G. Wiering.; H. Steinberg. The effect of pressure on the base-catalysed isomerizations of gem-dimethyl- and isopropyl-cyclohexenes. Part 6. Recueil des Travaux Chimiques des Pays-Bas. 1975, 94 (11), 243-245.