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Phenol, 4,4'-(dimethylsilylene)bis-, also known as bis(4-hydroxyphenyl)dimethylsilane, is an organosilicon compound characterized by its molecular formula C14H16O2Si. This chemical features a central dimethylsilane bridge connecting two phenol groups, which are aromatic compounds containing a hydroxyl group directly attached to a carbon atom on the benzene ring. The presence of the dimethylsilylene group imparts unique properties to Phenol, 4,4'-(dimethylsilylene)bis-, such as increased thermal stability and resistance to oxidation compared to the parent phenol molecule. Phenol, 4,4'-(dimethylsilylene)bis-, is utilized in various applications, including the synthesis of silane coupling agents, which are used to improve the adhesion between inorganic materials and organic polymers, as well as in the production of specialty resins and coatings. Its unique structure also makes it a subject of interest in materials science and organic chemistry research.

2915-36-8

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2915-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2915-36-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,1 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 2915-36:
(6*2)+(5*9)+(4*1)+(3*5)+(2*3)+(1*6)=88
88 % 10 = 8
So 2915-36-8 is a valid CAS Registry Number.

2915-36-8Relevant academic research and scientific papers

Design and synthesis of silicon-containing steroid sulfatase inhibitors possessing pro-estrogen antagonistic character

Kajita, Daisuke,Nakamura, Masaharu,Matsumoto, Yotaro,Makishima, Makoto,Hashimoto, Yuichi

, p. 2244 - 2252 (2014/04/17)

Steroid sulfatase (STS) is a potential target for treatment of postmenopausal hormone-dependent breast cancer. Several steroidal STS inhibitors have been reported, but steroidal compounds are difficult to optimize and may interact with other targets. On t

New insights into structure-property relationships in thermosetting polymers from studies of cocured polycyanurate networks

Guenthner, Andrew J.,Lamison, Kevin R.,Vij, Vandana,Reams, Josiah T.,Yandek, Gregory R.,Mabry, Joseph M.

experimental part, p. 211 - 220 (2012/04/17)

Studies of the physical properties of the cocured networks formed from three similar dicyanate ester monomers revealed a number of unexpected variations from simple linear mixing rules. These variations shed light on important synergistic effects in cocur

Synthesis and characterization of poly(carbonates) and poly(thiocarbonates) derived from diphenols containing silicon as central atom

Tagle,Terraza,Alvarez

, p. 239 - 248 (2007/10/03)

Poly(carbonates) and poly(thiocarbonates) containing silicon in the main chain and derived from the diphenols bis(4-hydroxyphenyl)-dimethylsilane, bis(4-hydroxyphenyl)-ethylmethylsilane, and bis(4-hydroxyphenyl)-diethylsilane with phosgene or thiophosgene

New bisphenols with silylene fragments: Synthesis and spectra

Pushkarev

, p. 1749 - 1751 (2007/10/03)

A series of bisphenols containing silylene sequences were prepared by condensation of 4-(trimethylsiloxy)phenylmagnesium bromide with αω-dichloropermethylsilanes and studied by fluorescence spectroscopy.

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