1956-79-2 Usage
Uses
Used in Organic Synthesis:
(Chloromethyl)(trifluoro)silane is used as a reagent in organic synthesis for the production of pharmaceuticals and agrochemicals. Its reactivity allows for the creation of a wide range of compounds with potential applications in these fields.
Used as a Silylating Agent:
In the field of material science, (Chloromethyl)(trifluoro)silane is used as a silylating agent to modify surfaces and introduce organosilicon functional groups into organic molecules. This modification can enhance the properties of materials, such as their stability or reactivity.
Used in Surface Modification:
(Chloromethyl)(trifluoro)silane is also utilized in the modification of surfaces, which can improve the performance of materials in various applications, including coatings, adhesives, and sealants.
Used in the Chemical Industry:
Within the chemical industry, (Chloromethyl)(trifluoro)silane is employed in the synthesis of various compounds, contributing to the development of new products and technologies.
Safety Precautions:
Check Digit Verification of cas no
The CAS Registry Mumber 1956-79-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,5 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1956-79:
(6*1)+(5*9)+(4*5)+(3*6)+(2*7)+(1*9)=112
112 % 10 = 2
So 1956-79-2 is a valid CAS Registry Number.
1956-79-2Relevant academic research and scientific papers
New route to 1,1-Difluoro-5-methylquasisilatrane
Soldatenko,Grebneva,Chernov,Albanov,Trofimova,Voronkov
experimental part, p. 2490 - 2492 (2012/04/10)
A new route to 1,1-difluoro-5-methylquasisilatrane (N→Si) F 2Si(OCH2CH2)2NMe is elaborated: the reaction of chlorinated methyltrifluorosilanes F3SiCH 3-nCln (n = 1-3) as well as trifluoro(3-chloropropyl) silane and trifluoro(propenyl)silane with N-methyl-bis(2-hydroxyethyl)amine. The reactivity of the silanes F3SiCH3-nCln increases with the number of chlorine atoms, that is, with the electronegativity of the CH3-nCln group. Pleiades Publishing, Ltd., 2011.
Infrared multiple photon dissociation of chloromethyltrifluorosilane
Koshlyakov, Pavel V.,Gorelik, Sergey R.,Chesnokov, Evgeniy N.,Aseev, Oleg S.,Rakhymzhan, Asylkhan A.,Petrov, Alexander K.
experimental part, p. 901 - 908 (2010/01/06)
Infrared multiphoton absorption and dissociation of chloromethyltrifluorosilane molecules under the action of pulsed transversely excited atmospheric pressure CO2 laser were experimentally studied. Dissociation products were analyzed. The dissociation proceeds via chlorine atom transfer from carbon to silicone. High degrees of silicon isotope separation were achieved. The presence of α-chlorine atom in a silicon organic compound brings about a significant improvement in multiple photon dissociation characteristics and an essential increase in isotopic selectivity.
