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Silane, methylenebis[dichloromethyl-], also known as bis(chloromethyl)methylsilane or Si(CClH2)3, is an organosilicon compound with the chemical formula C3H6Cl2Si. It is a colorless, volatile liquid that is highly reactive and sensitive to moisture and air. Silane, methylenebis[dichloromethyl- is primarily used as a coupling agent in the production of composite materials, such as fiberglass and carbon fiber, to improve the adhesion between the resin matrix and the reinforcing fibers. It is also employed as a cross-linking agent in the synthesis of silicone rubber and as a silylating agent in organic synthesis. Due to its reactivity, it is essential to handle this chemical with caution and under controlled conditions to prevent unwanted reactions and potential hazards.

4519-03-3

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4519-03-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4519-03-3 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 9 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4519-03:
(6*4)+(5*5)+(4*1)+(3*9)+(2*0)+(1*3)=83
83 % 10 = 3
So 4519-03-3 is a valid CAS Registry Number.

4519-03-3Relevant academic research and scientific papers

New chalcogen derivatives of silicon possessing adamantane and noradamantane structures

Herzog,Rheinwald

, p. 133 - 143 (2001)

The reaction of Si2Cl4Me2 (1) with Li2Se in THF yields exclusively the noradamantane (MeSi)4Se5 (4). The sulfur analogue (MeSi)4S5 (3) could be obtained from 1, MeSiCl

Synthesis of Functional Monosilanes by Disilane Cleavage with Phosphonium Chlorides

Santowski, Tobias,Sturm, Alexander G.,Lewis, Kenrick M.,Felder, Thorsten,Holthausen, Max C.,Auner, Norbert

supporting information, p. 3809 - 3815 (2019/02/13)

The Müller–Rochow direct process (DP) for the large-scale production of methylchlorosilanes MenSiCl4?n (n=1–3) generates a disilane residue (MenSi2Cl6?n, n=1–6, DPR) in thousands of tons annually. This report is on methylchlorodisilane cleavage reactions with use of phosphonium chlorides as the cleavage catalysts and reaction partners to preferably obtain bifunctional monosilanes MexSiHyClz (x=2, y=z=1; x,y=1, z=2; x=z=1, y=2). Product formation is controlled by the reaction temperature, the amount of phosphonium chloride employed, the choice of substituents at the phosphorus atom, and optionally by the presence of hydrogen chloride, dissolved in ethers, in the reaction mixture. Replacement of chloro by hydrido substituents at the disilane backbone strongly increases the overall efficiency of disilane cleavage, which allows nearly quantitative silane monomer formation under comparably moderate conditions. This efficient workup of the DPR thus not only increases the economic value of the DP, but also minimizes environmental pollution.

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