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(4-Fluorophenyl)Methyl-Trimethylsilane is an organosilicon compound that contains a silicon atom bonded to three methyl groups and a phenyl group with a fluorine atom attached to it. It is commonly used as a reagent in organic synthesis, particularly in the formation of carbon-silicon bonds. (4-Fluorophenyl)Methyl-Trimethylsilane is known for its ability to selectively introduce the (4-fluorophenyl)methyl group into various organic molecules, making it a valuable tool in chemical research and development. Additionally, (4-Fluorophenyl)Methyl-Trimethylsilane is considered to be relatively stable and can be safely handled and stored when following standard laboratory protocols.

706-25-2

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706-25-2 Usage

Uses

Used in Pharmaceutical Industry:
(4-Fluorophenyl)Methyl-Trimethylsilane is used as a reagent for the synthesis of pharmaceutical compounds, particularly for the introduction of the (4-fluorophenyl)methyl group into organic molecules. This allows for the creation of new drug candidates with potential therapeutic properties.
Used in Agrochemical Industry:
(4-Fluorophenyl)Methyl-Trimethylsilane is used as a reagent in the synthesis of agrochemicals, such as pesticides and herbicides. The introduction of the (4-fluorophenyl)methyl group can enhance the effectiveness of these compounds and contribute to the development of new agrochemical products.
Used in Specialty Chemicals Production:
(4-Fluorophenyl)Methyl-Trimethylsilane is used as a reagent in the production of specialty chemicals, where the selective introduction of the (4-fluorophenyl)methyl group can provide unique properties and applications for these chemicals. This can lead to the development of innovative materials and products in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 706-25-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 7,0 and 6 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 706-25:
(5*7)+(4*0)+(3*6)+(2*2)+(1*5)=62
62 % 10 = 2
So 706-25-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H15FSi/c1-12(2,3)8-9-4-6-10(11)7-5-9/h4-7H,8H2,1-3H3

706-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-fluorophenyl)methyl-trimethylsilane

1.2 Other means of identification

Product number -
Other names AMTSi095

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:706-25-2 SDS

706-25-2Relevant academic research and scientific papers

Fluoroalkylselenolation of Alkyl Silanes/Trifluoroborates under Metal-Free Visible-Light Photoredox Catalysis

Ghiazza, Clément,Khrouz, Lhoussain,Billard, Thierry,Monnereau, Cyrille,Tlili, Anis

supporting information, p. 1559 - 1566 (2019/11/03)

Herein a metal-free fluoroalkylselenolation of alkylsilanes as well as potassium alkyltrifluoroborates under visible light photocatalysis is disclosed. The developed methodologies are performed under mild conditions, room temperature in the presence of an organic photocatalyst and blue LED irradiation. Mechanistic investigations including luminescence and EPR spectroscopy allow us to shed light on both mechanisms.

Palladium-catalyzed C(sp3)-C(sp2) cross-coupling of homoleptic rare-earth metal trialkyl complexes with aryl bromides: Efficient synthesis of functionalized benzyltrimethylsilanes

Cai, Guilong,Huang, Yingda,Du, Tingting,Zhang, Shaowen,Yao, Bo,Li, Xiaofang

supporting information, p. 5425 - 5427 (2016/05/09)

The first C(sp3)-C(sp2) cross-coupling of rare-earth metal alkyl complexes with aryl bromides has been developed. This reaction was conducted at low catalyst loading (0.5 mol%) and exhibited a broad substrate scope, thus providing a facile method for the synthesis of benzyltrimethylsilanes with diverse functional groups.

Catalysis of Kumada-Tamao-Corriu coupling by a (POC OP)Rh pincer complex

Timpa, Samuel D.,Fafard, Claudia M.,Herbert, David E.,Ozerov, Oleg V.

supporting information; experimental part, p. 5426 - 5429 (2011/06/27)

A pincer-based (POCOP)Rh catalyst is demonstrated to be an active and well-defined catalyst for the coupling of select aryl and alkyl Grignards with aryl iodides. The proposed intermediacy of oxidative addition of aryl halides to (POCOP)RhI is supported by the isolation of the oxidative addition product. The Royal Society of Chemistry.

Reactions of a N-acyliminium ion pool with benzylsilanes. Implication of a radical/cation/radical cation chain mechanism involving oxidative C-Si bond cleavage

Maruyama, Tomokazu,Mizuno, Yusuke,Shimizu, Ikuo,Suga, Seiji,Yoshida, Jun-Ichi

, p. 1902 - 1903 (2007/10/03)

The reaction of a N-acyliminium ion pool with benzylsilane proceeds by a chain mechanism involving oxidative C-Si bond cleavage. A radical/cation/radical cation crossover mechanism involving single electron transfer has been proposed. The effective binary

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