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Silane, [2-methoxy-4-(2-propenyl)phenoxy]trimethyl-, is a complex organic compound with the chemical formula C13H24O2Si. It is a colorless liquid at room temperature and is derived from the combination of a silane molecule with a methoxy and allylphenoxy group. Silane, [2-methoxy-4-(2-propenyl)phenoxy]trimethyl- is primarily used as a coupling agent in the production of composite materials, particularly in the rubber and plastics industries, to enhance the adhesion between the inorganic and organic components. It is also employed as a cross-linking agent in the synthesis of various polymers, contributing to improved mechanical properties and durability of the final products. Due to its reactivity, it is essential to handle Silane, [2-methoxy-4-(2-propenyl)phenoxy]trimethyl- with care, following appropriate safety measures to prevent potential hazards.

4515-52-0

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4515-52-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4515-52-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,5,1 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4515-52:
(6*4)+(5*5)+(4*1)+(3*5)+(2*5)+(1*2)=80
80 % 10 = 0
So 4515-52-0 is a valid CAS Registry Number.

4515-52-0Relevant academic research and scientific papers

Synthesis of bifunctional disiloxanes: Via subsequent hydrosilylation of alkenes and alkynes

Szyling, Jakub,Januszewski, Rafa?,Jankowska, Kamila,Walkowiak, J?drzej,Kownacki, Ireneusz,Franczyk, Adrian

supporting information, p. 4504 - 4507 (2021/05/17)

The first protocol for the synthesis of unsymmetrical bifunctional 1,1,3,3-tetramethyldisiloxane derivatives via subsequent hydrosilylation of alkenes and alkynes is presented. The methodology described has vast functional group tolerance and is extremely efficient towards the formation of novel disiloxane-based building blocks.

Silyl derivatives of eugenol

-

, (2008/06/13)

Silyl derivatives of eugenol include compositions of the formula STR1 where R1, R2 and R3 are independently selected from linear, branched, and cyclic hydrocarbon groups having a total of from one to about eight carbon ato

29Si and 13C NMR Spectra of 4-Substituted 2-Methoxytrimethylsiloxybenzenes. Factors Determining the Chemical Shifts in Models of Lignin Constituents

Schraml, Jan,Kvicalova, Magdalena,Chvalovsky, Vaclav,Elder, Thomas,Brezny, Robert

, p. 973 - 978 (2007/10/02)

29Si and 13C NMR chemical shifts are reported for a series of twenty 4-substituted 2-methoxytrimethylsiloxybenzenes; the set of substituents incorporates a basic set of ten substituents differing in their relative polar and resonance effects and ten other

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