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bis[4-(3-nitro-5-trifluoromethylphenoxy)phenyl]sulfone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1206480-18-3

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1206480-18-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206480-18-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,4,8 and 0 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1206480-18:
(9*1)+(8*2)+(7*0)+(6*6)+(5*4)+(4*8)+(3*0)+(2*1)+(1*8)=123
123 % 10 = 3
So 1206480-18-3 is a valid CAS Registry Number.

1206480-18-3Relevant academic research and scientific papers

Preparation and characterization of highly transparent and colorless semi-aromatic polyimide films derived from alicyclic dianhydride and aromatic diamines

Zhai, Lei,Yang, Shiyong,Fan, Lin

, p. 3529 - 3539 (2012)

A novel meta-substituted aromatic diamine containing trifluoromethyl and sulfonyl groups in the backbone, i.e., 2,2′-bis[4-(3-amino-5- trifluoromethylphenoxy)phenyl]sulfone (m-6FBAPS), was synthesized and characterized. A series of semi-aromatic polyimides were prepared from 1,2,4,5-cyclohexanetetracarboxylic dianhydride (CHDA) and various aromatic diamines. These polymers exhibited excellent solubility, high thermal stabilities and good mechanical properties. All semi-aromatic polyimide films showed considerably improved optical transparency as comparing with traditional aromatic ones due to the incorporation of alicyclic moieties. They gave the UV cutoff wavelengths of 292-314 nm, transmittance at 450 nm > 91% and yellowness indices 3.8. The extremely transparent and entirely colorless films were obtained from the polymers incorporated with bulky electron-withdrawing trifluoromethyl and sulfonyl groups in diamine moieties, such as PI-2, PI-5 and PI-6. Their excellent optical properties are attributed to the distorted molecular conformation combined with the weakened electron-accepting and electron-donating properties of dianydride and diamines, which significantly restrained the formation of inter-/intra-molecular charge transfer interactions.

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