Grundinformationen
- Standard-SMILES
N#Cc1c(C(F)(F)F)cc(Cl)nc1Cl- InChIKey
WRXXBTBGBXYHSG-UHFFFAOYSA-N- Summenformel
- C7HCl2F3N2
- Durchschnittliche Molmasse
- 240,99 g/mol
- Monoisotopische Masse
- 239,94688805
Namen und Bezeichner
- Bevorzugter Name
- 2,6-Dichloro-4-(trifluoromethyl)nicotinonitrile
- IUPAC
- 2,6-dichloro-4-(trifluoromethyl)pyridine-3-carbonitrile
- Englischer Name
- 2,6-Dichloro-4-(trifluoromethyl)nicotinonitrile
- Summenformel
- C7HCl2F3N2
- Molmasse
- 241
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
13600-42-5- PubChem CID
- 2736726
- DTXSID
DTXSID50371555- EC Number
- 670-849-5
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 3,4
- Polarare Oberfläche (TPSA)
- 36,7 Ų
- H-Brücken-Donoren
- 0
- H-Brücken-Akzeptoren
- 5
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 14
- Formalladung
- 0
- Komplexität
- 259
Physikochemische Eigenschaften
- Schmelzpunkt
- 38 °C · 38 °C
- Siedepunkt
- 282.4 · 282.4±35.0 °C(Predicted)
- Dichte
- 1.63 · 1.63±0.1 g/cm3(Predicted)
- storage temp.
- 2 · under inert gas (nitrogen or Argon) at 2-8°C
- Aggregatzustand
- crystals
- pka
- -6.82 · -6.82±0.10(Predicted)
- Farbe
- Colourless
- CAS Datenbank
- 13600 · 13600-42-5(CAS DataBase Reference)
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H301 (25%): 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, P317, 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 4 reports by companies from 4 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- ridadr
- 3439
- hs_code
- 2933399990
- risk_code
- 20/21/22-36/37/38
- hazard_code
- T,Xi,Xn
- safety_code
- 22-26-36/37/39
- hazard_class
- TOXIC
Chemie und Industrie
Anwendungen
Verwenden3-Cyano-2,6-dichloro-4-trifluoromethylpyridine is used as a reagent in the synthesis of cyano(trifluoromethyl)aminopyridine derivatives which are used as androgen receptor antagonists for stimulating hair growth and reducing sebum production. 3-Cyano-2,6-dichloro-4-trifluoromethylpyridine is also used in the preparation of novel analogs of marine indole alkaloids which are used as potential anticancer agents.
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