1,1,1-Trifluoroacetone structure
|
Common Name | 1,1,1-Trifluoroacetone | ||
---|---|---|---|---|
CAS Number | 421-50-1 | Molecular Weight | 112.050 | |
Density | 1.2±0.1 g/cm3 | Boiling Point | 21.5±0.0 °C at 760 mmHg | |
Molecular Formula | C3H3F3O | Melting Point | -78 °C | |
MSDS | Chinese USA | Flash Point | -30.6±0.0 °C | |
Symbol |
GHS02, GHS07 |
Signal Word | Danger |
Name | 1,1,1-Trifluoroacetone |
---|---|
Synonym | More Synonyms |
Density | 1.2±0.1 g/cm3 |
---|---|
Boiling Point | 21.5±0.0 °C at 760 mmHg |
Melting Point | -78 °C |
Molecular Formula | C3H3F3O |
Molecular Weight | 112.050 |
Flash Point | -30.6±0.0 °C |
Exact Mass | 112.013596 |
PSA | 17.07000 |
LogP | 0.49 |
Vapour Pressure | 865.9±0.0 mmHg at 25°C |
Index of Refraction | 1.287 |
Storage condition | 2-8°C |
Water Solubility | Miscible |
Symbol |
GHS02, GHS07 |
---|---|
Signal Word | Danger |
Hazard Statements | H224-H315-H319-H335 |
Precautionary Statements | P210-P261-P305 + P351 + P338 |
Personal Protective Equipment | Eyeshields;Faceshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US) |
Hazard Codes | F+:Highlyflammable;Xi:Irritant; |
Risk Phrases | R12;R36/37/38 |
Safety Phrases | S16-S26-S29-S33-S36-S7/9-S9-S37/39 |
RIDADR | UN 1993 3/PG 1 |
WGK Germany | 3 |
Packaging Group | I |
Hazard Class | 3 |
HS Code | 29147090 |
Precursor 9 | |
---|---|
DownStream 9 | |
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% |
Mitochondrial dysfunction and respiratory chain defects in a rodent model of methotrexate-induced enteritis.
Hum. Exp. Toxicol. 33(10) , 1051-65, (2014) The efficacy of methotrexate (MTX), a widely used chemotherapeutic drug, is limited by its gastrointestinal toxicity and the mechanism of which is not clear. The present study investigates the possibl... |
|
Concise synthesis of enantiopure alpha-trifluoromethyl alanines, diamines, and amino alcohols via the Strecker-type reaction.
J. Org. Chem. 71 , 7075, (2006) Diastereomerically pure alpha-trifluoromethyl alpha-amino nitriles obtained by Strecker-type reactions from chiral CF3 imines and iminium proved to be very attractive versatile intermediates for the s... |
|
Synthesis , 251, (2007)
|
1,1,1-Trifluorpropan-2-on |
EINECS 207-005-9 |
1,1,1-Trifluoroacetone |
2-Propanone, 1,1,1-trifluoro- |
MFCD00000423 |
1,1,1-trifluoropropan-2-one |