| Identification | More | [Name]
2-TRIFLUOROMETHYL-2-PROPANOL | [CAS]
507-52-8 | [Synonyms]
1,1,1-TRIFLUORO-2-METHYL-2-PROPANOL
2-TRIFLUOROMETHYL-2-PROPANOL
2-(TRIFLUOROMETHYL)PROPAN-2-OL
2-(TRIFLUOROMETHYL)-PROPANOL-2
1,1,1-trifluoro-2-methyl-propan-2-ol
2-Propanol, 1,1,1-trifluoro-2-methyl-
2,2,2-Trifluoro-tert-Butanol
2-(Trifluoromethyl)propan-2-ol 98%
2-(Trifluoromethyl)propan-2-ol98%
2-TRIFLUOROMETHYL-2-PROPANOL 95% | [EINECS(EC#)]
208-075-3 | [Molecular Formula]
C4H7F3O | [MDL Number]
MFCD00014391 | [Molecular Weight]
128.09 | [MOL File]
507-52-8.mol |
| Chemical Properties | Back Directory | [Melting point ]
53℃ | [Boiling point ]
83 °C (lit.) | [density ]
1.17 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.3335(lit.)
| [Fp ]
59 °F
| [form ]
clear liquid | [pka]
12.60±0.29(Predicted) | [color ]
Colorless to Almost colorless | [BRN ]
1736196 | [InChI]
1S/C4H7F3O/c1-3(2,8)4(5,6)7/h8H,1-2H3 | [InChIKey]
OCGWWLDZAFOHGD-UHFFFAOYSA-N | [SMILES]
CC(C)(O)C(F)(F)F | [CAS DataBase Reference]
507-52-8(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
F | [Risk Statements ]
R11:Highly Flammable. | [Safety Statements ]
S16:Keep away from sources of ignition-No smoking .
S23:Do not breathe gas/fumes/vapor/spray (appropriate wording to be specified by the manufacturer) .
S36:Wear suitable protective clothing . | [RIDADR ]
1987 | [WGK Germany ]
3
| [Hazard Note ]
Flammable | [HazardClass ]
3 | [PackingGroup ]
II | [HS Code ]
2905599890 | [Storage Class]
3 - Flammable liquids | [Hazard Classifications]
Flam. Liq. 2 |
| Hazard Information | Back Directory | [Uses]
2-Trifluoromethyl-2-propanol may be employed as a solvent for the preparation of [18F]fluorothymidine. It may also be used in the synthesis of [2-(trifluoromethyl)-2-propyl nitrate] through nitration in nitric acid/trifluoroacetic anhydride. | [General Description]
2-Trifluoromethyl-2-propanol is a fluorinated aliphatic alcohol. It can be prepared by reacting methyllithium, trifluoroacetone and trifluorovinyl bromide in ether. This can also be synthesized from the reaction between methylmagnesium bromide and 1,1,1-trifluoroacetone in ether. |
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