5-(Trifluoromethyl)-1-indanone

5-(Trifluoromethyl)-1-indanone Suppliers list
Company Name: J & K SCIENTIFIC LTD.  
Tel: 18210857532 18210857532
Email: jkinfo@jkchemical.com
Company Name: Beijing HwrkChemical Technology Co., Ltd  
Tel: 89508211 18501085097
Email: sales.bj@hwrkchemical.com
Company Name: Tetranov Biopharm  
Tel: 13526569071
Email: sales@leadmedpharm.com
Company Name: Shanghai Hanhong Scientific Co.,Ltd.  
Tel: 021-54306202 13764082696
Email: info@hanhongsci.com
Company Name: China DongFan Chemical Co.,LTD  
Tel: 86-0571-85151182
Email:

5-(Trifluoromethyl)-1-indanone manufacturers

5-(Trifluoromethyl)-1-indanone Basic information
Product Name:5-(Trifluoromethyl)-1-indanone
Synonyms:5-(TRIFLUOROMETHYL)-2,3-DIHYDROINDEN-1-ONE,98%;5-(TRIFLUOROMETHYL)INDANONE;5-trifluormethyl-1-indanone;5-(Trifluoromethyl)-1-indanone;2,3-Dihydro-5-(trifluoromethyl)-1H-inden-1-one, 2,3-Dihydro-1-oxo-5-(trifluoromethyl)-1H-indene;5-(Trifluoromethyl)indan-1-one 98%;1H-Inden-1-one, 2,3-dihydro-5-(trifluoromethyl)-;5-(TrifluoroMethyl)-2,3-dihydro-1H-inden-1-one
CAS:150969-56-5
MF:C10H7F3O
MW:200.16
EINECS:
Product Categories:Indanone & Indene
Mol File:150969-56-5.mol
5-(Trifluoromethyl)-1-indanone Structure
5-(Trifluoromethyl)-1-indanone Chemical Properties
Boiling point 237.1±40.0 °C(Predicted)
density 1.347±0.06 g/cm3(Predicted)
storage temp. Sealed in dry,Room Temperature
solubility Chloroform (Slightly), DMSO (Slightly)
form Solid
color White to Off-White
Safety Information
HS Code 2914390090
MSDS Information
5-(Trifluoromethyl)-1-indanone Usage And Synthesis
Synthesis
2-bromo-5-(trifluoromethyl)-benzenepropanoic acid

869725-56-4

5-(Trifluoromethyl)-1-indanone

150969-56-5

Step E General procedure for the synthesis of 5-(trifluoromethyl)indan-1-one from 3-[2-bromo-5-(trifluoromethyl)phenyl]propionic acid: to a mixture of 3-[2-bromo-5-(trifluoromethyl)phenyl]propionic acid (2.8 g, 9.4 mmol) in THF (100 mL) and hexanes (20 mL) was added slowly and dropwise at -78°C a solution of 2.5 M n-butyllithium in hexane (8.3 mL). After dropwise addition, the reaction was quenched with saturated aqueous NH4Cl solution. The reaction mixture was extracted twice with ethyl acetate. The combined organic phases were washed with saturated aqueous NaHCO3 and brine, dried over anhydrous MgSO4 and concentrated. The crude product was purified by fast column chromatography on silica gel with 10-20% EtOAc/hexane as eluent to afford the target product 5-(trifluoromethyl)indan-1-one as a white solid (0.7 g, 37% yield).LC/MS analysis: the calculated value of (M+H)+ for C10H7F3O was 201; measured value, 201.1.

References[1] Patent: US2005/261310, 2005, A1. Location in patent: Page/Page column 25
[2] ACS Medicinal Chemistry Letters, 2010, vol. 1, # 9, p. 483 - 487
5-(Trifluoromethyl)-1-indanone Preparation Products And Raw materials
Raw materials2-bromo-5-(trifluoromethyl)-benzenepropanoic acid-->Hexane-->Tetrahydrofuran-->n-Butyllithium
Tag:5-(Trifluoromethyl)-1-indanone(150969-56-5) Related Product Information
Indan 1-Indanone 5-(Trifluoromethyl)-1-indanone 5-Methyl-1-indanone 2-Phenyl-5-(trifluoromethyl)-1H-indene-1,3(2H)-dione tert-Butyl 3-oxo-6-(trifluoromethyl)-2,3-dihydrospiro[indene-1,4'-piperidine]-1'-carboxylate 7-Bromo-6-fluoro-1-indanone 4-Bromo-6-fluoroindan-1-one 5-Chloro-7-hydroxy-indan-1-one 7-Bromo-4-fluoro-2,3-dihydro-1H-inden-1-one