1,1,1-Trifluoro-2-butanone

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Names

[ CAS No. ]:
381-88-4

[ Name ]:
1,1,1-Trifluoro-2-butanone

[Synonym ]:
1,1,1-Trifluoro-2-butanone
1,1,1-Trifluorobutan-2-one
MFCD00190641

Chemical & Physical Properties

[ Density]:
1.2±0.1 g/cm3

[ Boiling Point ]:
45.4±35.0 °C at 760 mmHg

[ Molecular Formula ]:
C4H5F3O

[ Molecular Weight ]:
126.077

[ Flash Point ]:
-8.8±17.4 °C

[ Exact Mass ]:
126.029251

[ PSA ]:
17.07000

[ LogP ]:
1.02

[ Vapour Pressure ]:
348.6±0.1 mmHg at 25°C

[ Index of Refraction ]:
1.314

MSDS

Safety Information

[ Symbol ]:

GHS02

[ Signal Word ]:
Danger

[ Hazard Statements ]:
H225

[ Precautionary Statements ]:
P210

[ Personal Protective Equipment ]:
Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US)

[ Hazard Codes ]:
F: Flammable;

[ Risk Phrases ]:
R11;R36/37/38

[ Safety Phrases ]:
S9-S16-S29-S33

[ RIDADR ]:
UN 1993 3/PG 1

[ WGK Germany ]:
3

[ Packaging Group ]:
II

[ Hazard Class ]:
3

[ HS Code ]:
2914700090

Synthetic Route

Precursor & DownStream

Precursor

  • Ethyl trifluoroacetate
  • ETHYLMAGNESIUM BROMIDE
  • ethane
  • Trifluoroacetic anhydride
  • ethyl 2-methyl-4,4,4-trifluoroacetoacetate
  • 1,1,1-trifluoro-2-butanol
  • Bromoethane
  • (trifluoro methyl) magnesiumiodide
  • Propanoyl chloride
  • ethylmagnesium iodide

DownStream

  • 3-BROMO-1,1,1-TRIFLUORO-2-BUTANONE
  • 1,1,1-trifluoro-N-(4-methoxyphenyl)butan-2-imine
  • 3-(trifluoromethyl)pent-1-yn-3-ol
  • 1,1,1-trifluoro-2-butanol
  • 3,3-Dibromo-2-oxo-1,1,1-trifluorobutane

Customs

[ HS Code ]: 2914700090

[ Summary ]:
HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%

Articles

A facile synthesis of C-24 and C-25 oxysterols by in situ generated ethyl(trifluoromethyl)dioxirane.

Steroids 74(1) , 81-7, (2009)

Experiments were performed to compare the regioselective hydroxylation of the isopropyl C-H bond at C-25 in 5alpha-cholestan-3beta-yl acetate by in situ generated dimethyldioxirane, methyl(trifluorome...


More Articles


Related Compounds

  • 3-BROMO-1,1,1-TRIFLUORO-2-BUTANONE
  • 1,1,1-Trifluoro-2-butanone cyanohydrin
  • 4,4-Diethoxy-1,1,1-trifluoro-2-butanone
  • 1,1,1-trifluoro-2-(1,1,2,2-tetrafluoroethoxy)propane
  • 1,1,1-Trifluoro-2-methyl-2-propanol
  • 1,1,1-trifluoro-2,4-heptanedione
  • N-{[1-methyl-3-(pyridin-4-yl)-1H-pyrazol-5-yl]methyl}-2,1,3-benzothiadiazole-5-carboxamide
  • Methyl 3-[[1-(2,2,2-trifluoroethyl)piperidin-4-yl]methylsulfamoyl]thiophene-2-carboxylate
  • N-{[1-methyl-3-(pyridin-2-yl)-1H-pyrazol-5-yl]methyl}-1,3-benzothiazole-2-carboxamide
  • N-(adamantan-1-yl)-3-oxo-4-(1,3-thiazol-2-yl)piperazine-1-carboxamide
  • N-{[1-methyl-3-(thiophen-2-yl)-1H-pyrazol-5-yl]methyl}adamantane-1-carboxamide
  • 4-methoxy-2-methyl-N-{[1-methyl-3-(pyridin-2-yl)-1H-pyrazol-5-yl]methyl}benzene-1-sulfonamide
  • 4-(5-fluoropyrimidin-2-yl)-3-oxo-N-[(thiophen-2-yl)methyl]piperazine-1-carboxamide
  • 1,3-Benzodioxol-5-yl-[3-(triazol-1-ylmethyl)azetidin-1-yl]methanone
  • 3-Tert-butyl-6-{[1-(2-phenyl-1,3-thiazole-4-carbonyl)piperidin-4-yl]methoxy}pyridazine
  • 4,4,4-trifluoro-N-{2-[4-(furan-2-yl)phenyl]-2-hydroxyethyl}butanamide
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