Zifrosilone

Zifrosilone Suppliers list
Company Name: Suzhou Meishi Biotechnology Co., Ltd.  
Tel: 1173954148q
Email: meishipharma@126.com
Products Intro: Product Name:132236-18-1
CAS:132236-18-1
Purity:99% HPLC Package:1G;5G;10G;100G;1KG;
Company Name: Zhuhai Aobokai Biomedical Technology Co., Ltd.  
Tel: 400-0628126
Email: sales-team@aobchem.com.cn
Products Intro: Product Name:2,2,2-trifluoro-1-(3-(trimethylsilyl)phenyl)ethanone
CAS:132236-18-1
Purity:95%+ Package:1g;5kg Remarks:86114
Company Name: Baoji Didu Pharmaceutical and Chemical Co., Ltd  
Tel: 17691182729 15991417702
Email: 1065@dideu.com
Products Intro: Product Name:2,2,2-trifluoro-1-(3-(trimethylsilyl)phenyl)ethanone
CAS:132236-18-1
Purity:95% Package:1kg;25kg
Company Name: TargetMol Chemicals Inc.  
Tel: 15002134094
Email: marketing@targetmol.com
Products Intro: Product Name:Zifrosilone
CAS:132236-18-1
Purity:详情请点击官网 Package:1 mg
Company Name: Lanospharma Laboratories Co.,Ltd  
Tel: 13440048448
Email: sales@lanospharma.com
Products Intro:
Zifrosilone Basic information
Product Name:Zifrosilone
Synonyms:Zifrosilone;MDL73745;Ethanone, 2,2,2-trifluoro-1-[3-(trimethylsilyl)phenyl]-;2,2,2-trifluoro-1-(3-(trimethylsilyl)phenyl)ethanone
CAS:132236-18-1
MF:C11H13F3OSi
MW:246.3
EINECS:
Product Categories:
Mol File:132236-18-1.mol
Zifrosilone Structure
Zifrosilone Chemical Properties
Boiling point 215.3±35.0 °C(Predicted)
density 1.11±0.1 g/cm3(Predicted)
Safety Information
MSDS Information
Zifrosilone Usage And Synthesis
OriginatorZifrosilone,Marion Merrell Dow
UsesInhibitor (acetylcholinesterase).
Manufacturing Process3-Trimethylsilyl-bromobenzene:
A mixture of 1,3-dibromobenzene (25.0 g, 106.4 mmol) and trimethylsilylchloride (11.6 g, 106.4 mmol) in diethyl ether (50 ml) was added dropwise in 1.5 hours on magnesium (2.59 g, 106.4 mmol) in diethyl ether (25 ml). Then the mixture was refluxed for 18 hours, cooled to 0°C, treated with 4 N HCl (75 ml). The organic layer was separated, washed with water, brine, dried over MgSO 4 and concentrated. 3-Trimethylsilylbromobenzene was obtained by fractional distillation as a colorless oil (13.4 g, 55% yield, b.p.: 55-62°C/0.8 mmHg.
2,2,2-Trifluoro-1-(3-trimethylsilylphenyl)ethanone:
To a solution of 3-trimethylsilylbromobenzene (7.62 g, 33.3 mmol) in diethyl ether (35 ml) was added 1.5 M n-butyl lithium in hexane (22.2 ml, 33.3 mmol) at 0°C over 10 min. Then the mixture was allowed to react 15 min at room temperature, cooled to -78°C and ethyl trifluoroacetate (14.2 g, 100 mmol) was added over 5 min. Then the mixture was allowed to react 15 min at -78°C, the cooling bath was removed and when the temperature rose to 0°C. 3 N HCl (35 ml) was added dropwise. The organic layer was separated, washed with water, brine, dried over MgSO 4 and concentrated. Chromatography (silica gel, cyclohexane/diethyl ether: 90/10) followed by distillation under reduced pressure afforded the expected compound (zifrosilone) as a colorless oil (4.32 g, 53% yield), boiling point 120°C/0.8 mm Hg; Rf: 0.28 (cyclohexane/diethyl ether: 95/5).
Therapeutic FunctionAcetylcholinesterase inhibitor
Zifrosilone Preparation Products And Raw materials
Raw materialsn-Butyllithium-->Chlorotrimethylsilane
Tag:Zifrosilone(132236-18-1) Related Product Information
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