CAS 30071-93-3|1-(3,5-Bis(trifluoromethyl)phenyl)ethanone

Introduction:Basic information about CAS 30071-93-3|1-(3,5-Bis(trifluoromethyl)phenyl)ethanone, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.
Common Name1-(3,5-Bis(trifluoromethyl)phenyl)ethanone
CAS Number30071-93-3Molecular Weight256.145
Density1.4±0.1 g/cm3Boiling Point162.7±35.0 °C at 760 mmHg
Molecular FormulaC10H6F6OMelting Point/
MSDSChineseUSAFlash Point82.2±0.0 °C
Symbol
GHS07
Signal WordWarning

Names

Name1-[3,5-bis(trifluoromethyl)phenyl]ethanone
SynonymMore Synonyms

Chemical & Physical Properties

Density1.4±0.1 g/cm3
Boiling Point162.7±35.0 °C at 760 mmHg
Molecular FormulaC10H6F6O
Molecular Weight256.145
Flash Point82.2±0.0 °C
Exact Mass256.032288
PSA17.07000
LogP4.06
Vapour Pressure2.1±0.3 mmHg at 25°C
Index of Refraction1.407
InChIKeyMCYCSIKSZLARBD-UHFFFAOYSA-N
SMILESCC(=O)c1cc(C(F)(F)F)cc(C(F)(F)F)c1

Safety Information

Symbol
GHS07
Signal WordWarning
Hazard StatementsH315-H319-H335
Precautionary StatementsP261-P305 + P351 + P338
Personal Protective EquipmentEyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter
Hazard CodesXi:Irritant
Risk PhrasesR36/37/38
Safety PhrasesS26-S36/37/39-S37/39
RIDADR3439
WGK Germany3
HS Code2914700090

Customs

HS Code2914700090
SummaryHS: 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%

Articles3

More Articles
Inhibition of monoamine oxidase-B by 5H-indeno[1,2-c]pyridazines: biological activities, quantitative structure-activity relationships (QSARs) and 3D-QSARs.

J. Med. Chem. 38 , 3874-83, (1995)

A large series (66 compounds) of indeno[1,2-c]pyridazin-5-ones (IPs) were synthesized and tested on their monoamine oxidase-A (MAO-A) and MAO-B inhibitory activity. All of the tested compounds acted p...

Asymmetric biocatalytic reduction of 3,5-bis(trifluoromethyl) acetophenone to (1R)-[3,5-bis(trifluoromethyl)phenyl] ethanol using whole cells of newly isolated Leifsonia xyli HS0904.

Appl. Microbiol. Biotechnol. 90(6) , 1897-904, (2011)

A novel bacterial strain HS0904 was isolated from a soil sample using 3,5-bis(trifluoromethyl) acetophenone as the sole carbon source. This bacterial isolate can asymmetrically reduce 3,5-bis(trifluor...

Rhodium-catalyzed heterogeneous enantioselective hydrogenation of 3, 5-di-(trifluoromethyl)-acetophenone. Hess R, et al.

J. Mol. Catal. A: Chem. 212(1) , 205-9, (2004)

Synonyms

EINECS 250-023-7
Ethanone, 1-[3,5-bis(trifluoromethyl)phenyl]-
3,5-Bis(Trifluoromethyl)Acetophenone
1-[3,5-Bis(trifluoromethyl)phenyl]ethan-1-one
1-Acetyl-3,5-bis(trifluoromethyl)benzene
MFCD00009910
1-[3,5-Bis(trifluoromethyl)phenyl]ethanone
3′,5′-Bis(trifluoromethyl)acetophenone
FXFFR CV1 EXFFF
3’,5’-Bis(trifluoromethyl)acetophenone
3,5-ditrifluoromethylacetophenone
1-(3,5-Bis(trifluoromethyl)phenyl)ethanone
3',5'-Bis(trifluoromethyl)acetophenone
MBT-AC
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