51501-87-2 Usage
Uses
Used in Chemical Synthesis:
Methoxy-dimethyl-(4-methylphenyl)silane is used as a reagent in the synthesis of organic compounds due to its high reactivity, facilitating the formation of new chemical bonds and structures.
Used in Pharmaceutical Industry:
In the pharmaceutical sector, methoxy-dimethyl-(4-methylphenyl)silane is utilized as a silanizing agent for modifying the surface properties of drug molecules, potentially enhancing their stability, solubility, and bioavailability.
Used in Agrochemical Industry:
Methoxy-dimethyl-(4-methylphenyl)silane is employed as a component in the formulation of agrochemicals, where it can improve the performance and effectiveness of pesticides and other agricultural chemicals by altering their surface interactions with plants and pests.
Used in Materials Science:
In the field of materials science, methoxy-dimethyl-(4-methylphenyl)silane is used as a surface modifier to enhance the properties of various materials, such as improving adhesion, durability, and resistance to environmental factors.
Check Digit Verification of cas no
The CAS Registry Mumber 51501-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,5,0 and 1 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51501-87:
(7*5)+(6*1)+(5*5)+(4*0)+(3*1)+(2*8)+(1*7)=92
92 % 10 = 2
So 51501-87-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H16OSi/c1-9-5-7-10(8-6-9)12(3,4)11-2/h5-8H,1-4H3
51501-87-2Relevant academic research and scientific papers
Synthesis of phenols via fluoride-free oxidation of arylsilanes and arylmethoxysilanes
Rayment, Elizabeth J.,Summerhill, Nick,Anderson, Edward A.
, p. 7052 - 7060 (2012/10/07)
Rapid, efficient methods have been developed to prepare phenols from the oxidation of arylhydrosilanes. The effects of arene substituents and fluoride promoters on this process show that while electron-deficient arenes can undergo direct oxidation from the hydrosilane, electron-rich aromatics benefit from silane activation via oxidation to the methoxysilane using homogeneous or heterogeneous transition metal catalysis. The combination of these two oxidations into a streamlined flow procedure involving minimal processing of reaction intermediates is also reported.
Photochemical protodesilylation of 2-R3Si-1,3-dimethoxybenzenes. Direct observation of β-silyl-substituted cyclohexadienyl cations
Lew, Calvin S. Q.,McClelland, Robert A.
, p. 11516 - 11520 (2007/10/02)
Irradiation (254 nm) of the title compounds 5 (R3Si = Me3Si, Ph2MeSi, and 4-XC6H4Me2Si with X = 4-MeO, 4-Me, H, 4-F, and 4-Cl) in 1,1,1,3,3,3-hexafluoroisopropyl alcohol (HFIP) results in q
