| Identification | More | [Name]
METHYL TRIFLUOROPYRUVATE | [CAS]
13089-11-7 | [Synonyms]
METHYL 3,3,3-TRIFLUOROPYRUVATE
METHYL TRIFLUOROPYRUVATE
RARECHEM AL BF 1300
TRIFLUOROPYRUVIC ACID METHYL ESTER
Methyl trifluoropyruvate 97%
Methyltrifluoropyruvate97% | [EINECS(EC#)]
629-146-9 | [Molecular Formula]
C4H3F3O3 | [MDL Number]
MFCD00114936 | [Molecular Weight]
156.06 | [MOL File]
13089-11-7.mol |
| Chemical Properties | Back Directory | [Appearance]
clear colorless to light yellow liquid | [Boiling point ]
86 °C(lit.)
| [density ]
1.529 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.332(lit.)
| [Fp ]
80 °F
| [storage temp. ]
Flammables area | [form ]
Liquid | [color ]
Clear colorless to light yellow | [Specific Gravity]
1.528 | [BRN ]
1863490 | [InChI]
InChI=1S/C4H3F3O3/c1-10-3(9)2(8)4(5,6)7/h1H3 | [InChIKey]
XGLLQDIWQRQROJ-UHFFFAOYSA-N | [SMILES]
C(OC)(=O)C(=O)C(F)(F)F | [CAS DataBase Reference]
13089-11-7(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
C,F,Xi | [Risk Statements ]
R10:Flammable. | [Safety Statements ]
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S16:Keep away from sources of ignition-No smoking . | [RIDADR ]
UN 1993 3/PG 3
| [WGK Germany ]
3
| [Hazard Note ]
Flammable | [HazardClass ]
3 | [PackingGroup ]
III | [HS Code ]
29183000 |
| Hazard Information | Back Directory | [Chemical Properties]
clear colorless to light yellow liquid | [Uses]
Methyl 3,3,3-trifluoropyruvate may be used in the synthesis of:
- 2-hydroxy-2-trifluoromethylbutan-4-olides
- 2-(trifluoromethyl)butan-4-olides
- 4-trifluoromethyl-(2H)-pyridazin-3-ones
- methyl 3-methoxy-2-trifluoromethylacrylate
| [General Description]
Methyl 3,3,3-trifluoropyruvate is an alkyl 3,3,3-trifluoropyruvate that can be synthesized using hexafluoropropene-1,2-oxide (HFPO) as a starting material. It reacts with aromatic amines, benzylic manoamines and diamines to form the corresponding hemiaminals. |
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