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2.4.6.8'-Tetramethyl-2'.4'.6'.8-tetraphenyl-cyclotetrasiloxan is a complex cyclic organosilicon compound characterized by its unique structure. It consists of a cyclotetrasiloxane ring, which is a four-membered ring containing silicon and oxygen atoms, with each silicon atom bonded to two oxygen atoms. The compound is further modified by the presence of four methyl groups (-CH3) attached to the silicon atoms and four phenyl groups (C6H5) connected to the oxygen atoms. This arrangement endows the molecule with specific properties, such as thermal stability and resistance to hydrolysis, making it potentially useful in various applications, including as a component in high-performance materials and coatings. The compound's structure also contributes to its unique electronic and optical properties, which can be exploited in the development of advanced materials for electronics and photonics.

5131-04-4

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5131-04-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5131-04-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,1,3 and 1 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 5131-04:
(6*5)+(5*1)+(4*3)+(3*1)+(2*0)+(1*4)=54
54 % 10 = 4
So 5131-04-4 is a valid CAS Registry Number.

5131-04-4Downstream Products

5131-04-4Relevant academic research and scientific papers

A functionality do not contain impurity methyl phenyl cyclosiloxane method for the preparation of

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Paragraph 0048; 0049; 0054, (2017/04/29)

The invention relates to a preparation method of methylphenyl cyclosiloxane without containing polyfunctional impurities. The preparation method comprises the following steps: (A) sequentially adding a polar aprotic solvent, methylphenyl dialkoxysilane, water and a catalyst into a reactor for hydrolysis and condensation reaction, distilling out alcohol and water, and when the refractive index nD25 of distillate is nearly 1.3325, stopping the reaction; (2) gradually heating to 110-160 DEG C, and cracking the catalyst in a refluxing state; (3) after cracking the catalyst, distilling out and recycling the solvent, wherein an undistilled part in the reactor is a crude product; (4) distilling and purifying the crude product, and collecting methylphenyl cyclosiloxane distillate, namely obtaining a finished product. In the whole process, organic acid, inorganic acid or an alkali metal hydroxide is not used as a catalyst, and complex operations, such as neutralizing, water washing, filtering and the like rare not required; the reaction is easy to control; the yield of the finished product is as high as 90.0-97.1%; the purity of the finished product is 98.1-99.99%.

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