Grundinformationen
- CAS
645-59-0- Standard-SMILES
N#CCCc1ccccc1- InChIKey
ACRWYXSKEHUQDB-UHFFFAOYSA-N- Summenformel
- C9H9N
- Durchschnittliche Molmasse
- 131,17 g/mol
- Monoisotopische Masse
- 131,07349929
Überblick
3-phenylpropionitrile is a nitrile that is propionitrile in which one of the methyl hydrogens has been replaced by a phenyl group. It is a nitrile and a member of benzenes. It is functionally related to an acetonitrile.
Namen und Bezeichner
- Bevorzugter Name
- Benzenepropanenitrile
- IUPAC
- 3-phenylpropanenitrile
- Lokaler Name
- 3-Phenylpropiononitril
- Englischer Name
- 3-PHENYLPROPIONITRILE
- Summenformel
- C9H9N
- Molmasse
- 131.17
Namen und Synonyme
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Datenbank-Bezeichner
- CAS
645-59-0- PubChem CID
- 12581
- DTXSID
DTXSID4060949- ChEBI
CHEBI:85426- UNII
- H2Y1JYN13Q
- EC Number
- 211-447-8
- Nikkaji
- J45.903H
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 1,7
- Polarare Oberfläche (TPSA)
- 23,8 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 1
- Frei drehbare Bindungen
- 2
- Schwere Atome
- 10
- Formalladung
- 0
- Komplexität
- 125
Experimentelle und physikochemische Eigenschaften
LogP
1.72
1.72
Physikochemische Eigenschaften
- Schmelzpunkt
- 2 · −2-−1 °C(lit.)
- Siedepunkt
- 113 °C9 · 113 °C9 mm Hg(lit.)
- Dichte
- 1.001 g/mL · 1.001 g/mL at 25 °C(lit.)
- Brechungsindex
- 20 · n20/D 1.521(lit.)
- Flammpunkt
- 230 °F · >230 °F
- storage temp.
- Sealed in dry,Room Temperature
- Löslichkeit
- 1.68 g/l · 1.68g/l (calculated)
- Aggregatzustand
- Liquid
- Wichte
- 1 · 1
- Farbe
- Clear colorless to light yellow
- Geruch (Odor)
- powerful nasturtium
- BRN
- 636348 · 636348
- InChI
- 1S/C9H9N/c10-8-4-7-9-5-2-1-3-6-9/h1-3,5-6H,4,7H2
- InChIKey
- ACRWYXSKEHUQDB-UHFFFAOYSA-N
- SMILES
- N#CCCc1ccccc1
- CAS Datenbank
- 645 · 645-59-0(CAS DataBase Reference)
- EPA chemische Informationen
- Benzenepropanenitrile (645-59-0)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H301 (80.7%): Toxic if swallowed [Danger Acute toxicity, oral]
P261, P262, P264, P264+P265, P270, P271, P280, P301+P316, P301+P317, P302+P352, P304+P340, P305+P351+P338, P316, P319, P321, P330, P332+P317, P337+P317, P361+P364, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 57 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- wgk
- 3
- tsca
- TSCA listed
- ridadr
- UN 3276 6.1/PG 3
- hs_code
- 29269095
- RTECS-Nr.
- MW5604750
- risk_code
- 23/24/25-36-34
- hazard_code
- T,C
- safety_code
- 36/37/39-45-27-26
- hazard_class
- 6.1
- packing_group
- II
- Speicherklasse
- 6.1C - Combustible acute toxic Cat.3toxic compounds or compounds which causing chronic effects
- Hazard Classifications
- Acute Tox. 3 Oral
Chemie und Industrie
Pharmakologische Informationen
Verwendung und Herstellung
Anwendungen
Verwenden3-Phenylpropionitrile was used to study the free enzyme activity of nitrilase AtNIT1.
Darstellung
synthetischeTo a stirred solution of 3-phenylpropanamide (50 mg, 0.34 mmol) in acetonitrile (0.8 mL) at room temperature were successively added formic acid (0.2 mL) and paraformaldehyde (50 mg, 1.67 mmol). The reaction mixture was then refluxed for 12 h, and the solution obtained was cooled to room temperature. Work-up A: The crude mixture was concentrated under reduced pressure, and the residue was subjected to flash chromatography on silica gel (230–240 mesh) eluting with hexane/ethyl acetate (7:3) to yield 3-phenylpropanonitrile (37 mg, 85%). Work-up B: The reaction mixture was diluted with ethyl acetate (10 mL) and washed successively with saturated sodium hydrogen carbonate solution (5 mL) and water (5 mL). The combined aqueous layers were extracted with ethyl acetate (2 × 10 mL). The combined organic layers were dried over Na2SO4, filtered, and concentrated. The crude 3-phenylpropanonitrile was purified as described above (Work-up A).
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Ergänzende Hinweise
DefinitionChEBI: A nitrile that is propionitrile in which one of the methyl hydrogens has been replaced by a phenyl group.
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