62244-51-3 Usage
General Description
(4-chlorophenyl)(fluoro)dimethylsilane is a chemical compound with the molecular formula C8H10ClFSi. It is a silane derivative with a chlorine atom and a fluorine atom attached to a phenyl ring, as well as two methyl groups attached to the silicon atom. (4-chlorophenyl)(fluoro)dimethylsilane is used as a reagent in organic synthesis, particularly in the preparation of organosilicon compounds. It can also be used as a building block in the production of pharmaceuticals and agrochemicals. Additionally, (4-chlorophenyl)(fluoro)dimethylsilane has applications in the field of materials science, especially in the development of polymers and coatings with enhanced properties. Due to its reactive nature and potential toxicity, proper handling and safety precautions are necessary when working with this chemical.
Check Digit Verification of cas no
The CAS Registry Mumber 62244-51-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,2,4 and 4 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62244-51:
(7*6)+(6*2)+(5*2)+(4*4)+(3*4)+(2*5)+(1*1)=103
103 % 10 = 3
So 62244-51-3 is a valid CAS Registry Number.
62244-51-3Relevant articles and documents
Preparation of the iodides (Me3Si)2C(SiMe2C6H4Y)(SiMe2I) and some related compounds
Eaborn, Colin,Jones, Karen L.,Lickiss, Paul D.
, p. 35 - 42 (2007/10/02)
The preparations of: (a) the iodides (Me3Si)2C(SiMe2C6H4Y)(SiMe2I) (Y=H, p-OMe, p-Me, p-Cl, m-CF3), via the corresponding hydrides; (b) the compounds (Me3Si)2C(SiMe2Ph)(SiMe2X) with X=F, O2CCF3, OMe, N3, NCS and Cl: and (c) the iodide (p-MeC6H4)3CSiMe2I are described. Key words: Silicon; Iodide; Fluoride; Hydride; Trimethylsilyl
REACTIONS IN THE CHLOROSILANE-SILANOL-SILOXANE SYSTEM
Ruehlmann, K.
, p. 139 - 152 (2007/10/02)
We obtained the first ?*-values and ES-values for siloxy groups by spectroscopic and kinetic methods.Detailed mechanistic investigations are performed on the hydrolysis of chlorosilanes, the cleavage of Si-O-Si bonds by HCl, and the substituent exchange reaction between silanols and chlorosilanes.
