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1,1,1-Trifluoroacetone

Basic information Safety Supplier Related

1,1,1-Trifluoroacetone Basic information

Product Name:
1,1,1-Trifluoroacetone
Synonyms:
  • TRIFLUOROACETONE
  • 1,1,1-trifluoro-2-propanon
  • 3,3,3-Trifluoroacetone
  • CH3COCF3
  • Methyl trifluoromethyl ketone
  • Trifluoromethyl methyl ketone
  • 1,1,1-TRIFLUOROACETONE
  • 1,1,1-TRIFLUORO-2-PROPANONE
CAS:
421-50-1
MF:
C3H3F3O
MW:
112.05
EINECS:
207-005-9
Product Categories:
  • C3 to C6
  • Carbonyl Compounds
  • Ketones
Mol File:
421-50-1.mol
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1,1,1-Trifluoroacetone Chemical Properties

Melting point:
-78 °C
Boiling point:
22 °C(lit.)
Density 
1.252 g/mL at 25 °C(lit.)
vapor pressure 
13.62 psi ( 20 °C)
refractive index 
n20/D 1.3(lit.)
Flash point:
−23 °F
storage temp. 
2-8°C
solubility 
Chloroform, Methanol
form 
Liquid
color 
Clear colorless
Water Solubility 
Miscible
Sensitive 
Lachrymatory
BRN 
1748614
Stability:
Volatile
InChIKey
FHUDAMLDXFJHJE-UHFFFAOYSA-N
CAS DataBase Reference
421-50-1(CAS DataBase Reference)
NIST Chemistry Reference
2-Propanone, 1,1,1-trifluoro-(421-50-1)
EPA Substance Registry System
2-Propanone, 1,1,1-trifluoro- (421-50-1)
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Safety Information

Hazard Codes 
F+,Xi,F
Risk Statements 
12-36/37/38
Safety Statements 
16-26-29-33-36-7/9-9-37/39-39
RIDADR 
UN 1993 3/PG 1
WGK Germany 
3
19
Hazard Note 
Flammable/Lachrymatory
TSCA 
T
HazardClass 
3
PackingGroup 
I
HS Code 
29147090

MSDS

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1,1,1-Trifluoroacetone Usage And Synthesis

Chemical Properties

1,1,1-Trifluoroacetone is CLEAR COLOURLESS LIQUID

Uses

1,1,1-Trifluoroacetone is used as intermediate of bioactive substance and antihypertensive drug, and as effective synthetic building block and trifluoromethyl reaction reagent.

Uses

1,1,1-Trifluoroacetone is a general chemical reagent used in the synthesis of glucokinase-glucokinase regulatory protein) GK-GKRP disruptors which may act as potential targets for type II diabetics. Reactant for enantioselective cycloadditions.

Uses

Used in a synthesis of 2-trifluoromethyl-7-azaindoles starting with 2,6-dihalopyridines. The derived chiral imine was used to prepare enantiopure α-trifluoromethyl alanines and diamines via a Strecker reaction followed by either nitrile hydrolysis or reduction.

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