706-25-2 Usage
General Description
(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 has applications in the pharmaceutical and agrochemical industries, as well as in the production of specialty chemicals. It 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.
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
706-25-2Relevant articles and documents
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.
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.
