Grundinformationen
- Standard-SMILES
C[C@H](O)C(F)(F)F- InChIKey
GILIYJDBJZWGBG-REOHCLBHSA-N- Summenformel
- C3H5F3O
- Durchschnittliche Molmasse
- 114,07 g/mol
- Monoisotopische Masse
- 114,02924944
Namen und Bezeichner
- Bevorzugter Name
- (2S)-1,1,1-Trifluoropropan-2-ol
- IUPAC
- (2S)-1,1,1-trifluoropropan-2-ol
- Englischer Name
- (S)-1,1,1-TRIFLUORO-2-PROPANOL
- Summenformel
- C3H5F3O
- Molmasse
- 114.07
Namen und Synonyme
Weitere Namen anzeigen
Datenbank-Bezeichner
- CAS
3539-97-7- PubChem CID
- 6999971
- DTXSID
DTXSID10426459- EC Number
- 690-088-2
- Nikkaji
- J52.780G
Eigenschaften
Berechnete Struktureigenschaften
- XLogP
- 0,7
- Polarare Oberfläche (TPSA)
- 20,2 Ų
- H-Brücken-Donoren
- 1
- H-Brücken-Akzeptoren
- 4
- Frei drehbare Bindungen
- 0
- Schwere Atome
- 7
- Formalladung
- 0
- Komplexität
- 57,7
Physikochemische Eigenschaften
- Siedepunkt
- 67 · 67.0±35.0℃ (760 Torr)
- Dichte
- 1.235 · 1.235±0.06 g/cm3 (20 ºC 760 Torr)
- Flammpunkt
- 38.8 · 38.8±17.0℃
- storage temp.
- Store at room temperature
- pka
- 12.53 · 12.53±0.20(Predicted)
- Aggregatzustand
- liquid
- Farbe
- Clear
- InChI
- InChI=1S/C3H5F3O/c1-2(7)3(4,5)6/h2,7H,1H3/t2-/m0/s1
- InChIKey
- GILIYJDBJZWGBG-REOHCLBHSA-N
- SMILES
- C(F)(F)(F)[C@@H](O)C
Sicherheit und Regulatorisches
GHS-Klassifizierung
GHS Classification
Danger
H225 (100%): Highly Flammable liquid and vapor [Danger Flammable liquids]
P210, P233, P240, P241, P242, P243, P261, P264, P264+P265, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P319, P321, P332+P317, P337+P317, P362+P364, P370+P378, P403+P233, P403+P235, P405, and P501 (click each P-code to see the statement)
Aggregated GHS information provided per 5 reports by companies from 3 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.
Gefahrenhinweise
Sicherheitsdaten
- ridadr
- UN1993
- hs_code
- 2905599890
Chemie und Industrie
Anwendungen
Beschreibung(S)-1,1,1-Trifluoro-2-propanol is a compound important as an intermediate for various medicines and agrichemicals. Aside from methods using chemical catalysts, biological methods of reducing 1,1,1-trifluoroacetone to (S)-1,1,1-trifluoro-2-propanol by having microbial enzymes act on 1,1,1-trifluoroacetone has hitherto been studied.
Verwenden(S)-1,1,1-TRIFLUORO-2-PROPANOL can be used as organic synthesis intermediates and pharmaceutical intermediates, mainly used in laboratory research and development and chemical production processes.
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