3',5'-Bis(trifluoromethyl)acetophenone

3',5'-Bis(trifluoromethyl)acetophenone
  • CAS No.:30071-93-3
Other grades of this product :
3',5'-Bis(trifluoromethyl)acetophenone Basic information
Uses
Product Name:3',5'-Bis(trifluoromethyl)acetophenone
Synonyms:TRIFLUOROMETHYL ACETOPHENONE;3',5'-Bis(trifluoromethyl)acetophenone 98%;3,5-BIS(TRIFLUOROMETHYL);3,5-Di(trifluoromethyl)hypnone;3',5'-Bis(trifluorom;1-[3,5-bis(trifluoromethyl)phenyl]ethan-1-one;3.5-Bis(trifluoromethyl)acetopenone;1-[3,5-bis(trifluoromethyl)phenyl]ethanone (Aprepitant)
CAS:30071-93-3
MF:C10H6F6O
MW:256.14
EINECS:250-023-7
Product Categories:C10;Carbonyl Compounds;Boronic Acid series;PHARMACEUTICAL INTERMEDIATES;Miscellaneous;Ketones;Fluorides;Trifluoromethylbenzene serise;Aromatic Acetophenones & Derivatives (substituted);ketone;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks;Indolines ,Indoles
Mol File:30071-93-3.mol
3',5'-Bis(trifluoromethyl)acetophenone Chemical Properties
Boiling point 95-98 °C (15 mmHg)
density 1.422 g/mL at 25 °C(lit.)
refractive index n20/D 1.4221(lit.)
Fp 180 °F
storage temp. Sealed in dry,Room Temperature
form clear liquid
color Colorless to Light yellow
Specific Gravity1.422
BRN 2384789
CAS DataBase Reference30071-93-3(CAS DataBase Reference)
NIST Chemistry Reference3',5'-Bis(trifluoromethyl)acetophenone(30071-93-3)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36/37/39-37/39-36
RIDADR 3439
WGK Germany 3
HazardClass IRRITANT
HS Code 29147000
MSDS Information
ProviderLanguage
3',5'-Bis(trifluoromethyl)acetophenone English
ACROS English
SigmaAldrich English
ALFA English
3',5'-Bis(trifluoromethyl)acetophenone Usage And Synthesis
Uses3',5'-Bis(Trifluoromethyl)acetophenone is a reactant that has been used in the preparation of pyrazole carboxamide derivatives with antibacterial and antifungal activity.
Chemical PropertiesCLEAR PALE YELLOW LIQUID
Uses3'',5''-Bis(Trifluoromethyl)acetophenone is a reactant that has been used in the preparation of pyrazole carboxamide derivatives with antibacterial and antifungal activity.
Synthesis Reference(s)The Journal of Organic Chemistry, 68, p. 3695, 2003 DOI: 10.1021/jo026903n

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