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3-methyl-1-(triethylsiloxy)butane is an organic compound with the molecular formula C11H26OSi. It is a colorless liquid that is soluble in organic solvents. 3-methyl-1-(triethylsiloxy)butane is characterized by a butane chain with a methyl group at the third carbon and a triethylsiloxy group attached to the first carbon. The triethylsiloxy group consists of a silicon atom bonded to three ethyl groups and an oxygen atom. This structure endows the compound with unique chemical properties, making it useful in various applications, such as a protecting group in organic synthesis or as an intermediate in the preparation of other organosilicon compounds. Its stability and reactivity can be influenced by the presence of the siloxy group, which can participate in various chemical reactions, including hydrolysis and condensation reactions.

7030-73-1

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7030-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7030-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,0,3 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 7030-73:
(6*7)+(5*0)+(4*3)+(3*0)+(2*7)+(1*3)=71
71 % 10 = 1
So 7030-73-1 is a valid CAS Registry Number.

7030-73-1Relevant academic research and scientific papers

Alcoholysis Equilibria of Triethylalkoxysilanes Catalyzed by Iodine or Iodine Monobromide

Ito, Katsuko,Ibaraki, Takeshi

, p. 2973 - 2975 (2007/10/02)

The equilibrium constants K of alcoholysis of triethylalkoxysilanes were determined at 20 degC and 40 degC.Iodine monobromide was used to promote the reactions associated with the tertiary alkoxyl groups, while the other reactions proceeded in the presence of iodine.The K values of the reaction systems with ethoxyl or propoxyl-primary, secondary, and tertiary alkoxyl pairs were 1 or above, about 0.5, and about 0.05, respectively.These values reflect the extent of the binding abilities of the alkoxyl groups to silicon, which is in the expected order of primary>secondary>tertiary alkoxyl groups.A mechanism is postulated for the reaction which involves participation by the iodine or iodine monobromide.

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