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4,4'-Di(trimethylsilylamino)-diphenylmethan, also known as bis(trimethylsilyl)diphenylmethylamine, is an organosilicon compound characterized by its molecular formula C17H25NSi2. This chemical features a central diphenylmethylamine unit, with two trimethylsilyl groups attached to the nitrogen atoms. It is a colorless, viscous liquid that is soluble in common organic solvents. Due to its unique structure, it is often used as a reagent in organic synthesis, particularly in the formation of various silicon-containing compounds. The compound is also known for its thermal stability and resistance to hydrolysis, making it a valuable intermediate in the synthesis of specialty chemicals and materials.

1767-02-8

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1767-02-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1767-02-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,6 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1767-02:
(6*1)+(5*7)+(4*6)+(3*7)+(2*0)+(1*2)=88
88 % 10 = 8
So 1767-02-8 is a valid CAS Registry Number.

1767-02-8Downstream Products

1767-02-8Relevant academic research and scientific papers

Kinetic study of low-temperature imidization of poly(amic acid)s and preparation of colorless, transparent polyimide films

Yu, Hwan-Chul,Jung, Jae-Woo,Choi, Ju-Young,Chung, Chan-Moon

, p. 1593 - 1602 (2016)

Conventional synthesis of polyimides includes high-temperature (160-350 °C) imidization of poly(amic acid)s. In the present work, imidization has been carried out at much lower temperatures (40-160 °C). 1,2,4,5,-cyclohexanetetracarboxylic dianhydride (HPMDA) or pyromellitic dianhydride (PMDA) was polymerized with an aromatic diamine, 4,4′-diaminodiphenylmethane (DDPM), to give poly(amic acid)s, which were then imidized chemically. Imidization was more than 90% complete even at the very low imidization temperature of 40 °C. It was found that the imidization occurs in two steps: an initial rapid cyclization and a subsequent slower cyclization. The activation energy for the rapid process was determined to be 4.3 kJ/mol, and that of the slower process, 4.8 kJ/mol. As the imidization temperature decreases, the transmittance of the resulting polyimides tends to gradually increase, the cutoff wavelength decreases and the color becomes pale. A partially aliphatic polyimide based on HPMDA and DDPM prepared at 40 °C yielded thin films that were highly transparent and colorless, and had good flexibility, solubility and thermal stability. The polyimide films prepared in this study may be good candidates for flexible, transparent plastic substrates in the display industry.

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