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(Chloromethyl)bis(4-fluorophenyl)methylsilane, with the chemical formula C9H10ClFSi, is a silane compound characterized by a silicon atom bonded to two methyl groups, a chloromethyl group, and two 4-fluorophenyl groups. This versatile compound serves as a valuable building block in organic synthesis for the creation of complex molecules.

85491-26-5

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85491-26-5 Usage

Uses

Used in Organic Synthesis:
(Chloromethyl)bis(4-fluorophenyl)methylsilane is used as a versatile building block for the creation of complex molecules in organic synthesis. Its unique structure allows for the formation of various silanes and organosilicon compounds, contributing to the development of novel materials and compounds.
Used in Pharmaceutical and Agrochemical Industries:
(Chloromethyl)bis(4-fluorophenyl)methylsilane is used as a potential reagent for the preparation of pharmaceuticals and agrochemicals. Its ability to form diverse silane and organosilicon compounds makes it a valuable precursor in the synthesis of new drugs and agrochemicals, potentially leading to advancements in these fields.
Used in Materials Science:
(Chloromethyl)bis(4-fluorophenyl)methylsilane may find applications in materials science due to its potential to form functionalized silicones and other organosilicon compounds. These materials can be utilized in various applications, such as coatings, adhesives, and sealants, due to their unique properties.
Used as a Starting Material for Silicone Production:
(Chloromethyl)bis(4-fluorophenyl)methylsilane can be used as a starting material for the production of functionalized silicones. These silicones have a wide range of applications, including in the manufacturing of high-performance materials for various industries, such as electronics, automotive, and aerospace.

Check Digit Verification of cas no

The CAS Registry Mumber 85491-26-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,9 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85491-26:
(7*8)+(6*5)+(5*4)+(4*9)+(3*1)+(2*2)+(1*6)=155
155 % 10 = 5
So 85491-26-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H13ClF2Si/c1-18(10-15,13-6-2-11(16)3-7-13)14-8-4-12(17)5-9-14/h2-9H,10H2,1H3

85491-26-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (chloromethyl)bis(4-fluorophenyl)methylsilane

1.2 Other means of identification

Product number -
Other names (Chlormethyl)bis(4-fluorphenyl)methylsilan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:85491-26-5 SDS

85491-26-5Downstream Products

85491-26-5Relevant academic research and scientific papers

Flusilazole and synthesis method thereof

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Paragraph 0033-0038; 0043-0044; 0048-0049; 0053-0054, (2018/12/14)

The invention discloses flusilazole and a synthesis method thereof. The synthesis method comprises the following steps: putting magnesium powder into a Grignard reaction kettle; adding an organic solvent and uniformly stirring; cooling and adding p-fluorobromobenzene in one step; mixing and stirring; dropwise adding the p-fluorobromobenzene, and keeping heat and reacting; cooling and storing to obtain a p-fluorobromobenzene Grignard reagent; raising the temperature of the p-fluorobromobenzene Grignard reagent; dropwise adding methyl chloromethyl dichlorosilane and carrying out heat insulation;recycling an organic solvent under negative pressure to obtain a flusilazole intermediate, magnesium bromide and magnesium chloride; adding DMF (Dimethyl Formamide), stirring, cooling and centrifuging; removing the magnesium bromide and the magnesium chloride to obtain a DMF mother solution; dissolving triazole sodium salt into formamide; adding the DMF mother solution and reacting; recycling theDMF under negative pressure and distilling in vacuum; cooling to obtain the flusilazole. The content of the flusilazole is greater than or equal to 95.0 percent and the yield is 80 to 90 percent; thesynthesis method has the advantages of moderate reaction conditions, safety in operation, low equipment requirements, low cost, no wastewater and easiness for operation and implementation, and is suitable for large-scale production of enterprises.

Fungicidal 1,2,4-triazole derivatives

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, (2008/06/13)

Silicon-containing 1,2,4-triazoles having broad-spectrum fungicidal activity have been discovered.

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