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1,1,3,3,5-pentaphenoxy-5-[(4-hydroxy)phenoxy]-cyclotriphosphazatriene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

151340-07-7

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151340-07-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 151340-07-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,1,3,4 and 0 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 151340-07:
(8*1)+(7*5)+(6*1)+(5*3)+(4*4)+(3*0)+(2*0)+(1*7)=87
87 % 10 = 7
So 151340-07-7 is a valid CAS Registry Number.

151340-07-7Upstream product

151340-07-7Downstream Products

151340-07-7Relevant academic research and scientific papers

Elastomeric Polyphosphazenes with Phenoxy-Cyclotriphosphazene Side Groups

Modzelewski, Tomasz,Wilts, Emily,Allcock, Harry R.

, p. 7543 - 7549 (2015)

New polymers with a phosphazene backbone and both 2,2,2-trifluoroethoxy- and phenoxy-functionalized cyclotriphosphazene substituents exist in three phases depending on the side group ratios. At low concentrations of the bulky substituents (up to ~7 mol %), the polymers are semicrystalline thermoplastics, with properties that are minor variations of poly[bis(2,2,2-trifluoroethoxy)phosphazene]. However, after the incorporation of between ~7 mol % and ~20 mol % of the bulky cyclic trimeric side groups, the polymers lose their semicrystalline properties and become amorphous elastomers. At still higher trimer loadings (>20 mol %) the materials develop gum-like behavior. The elastomeric phase appears to be generated by interdigitation or agglomeration of the bulky aryloxy-cyclotriphosphazene side groups, which act as quasi-physical cross-links between the polymer chains. The presence of these interactions allows the materials to experience high strain values before rupture (up to 1000%), and elastic recovery of more than 85% of the original dimensions when stressed up to 60% of the break elongation over four cycles. In addition, the chemical and physical nature of the substituents on the cyclic trimeric side groups alters the physical characteristics of the polymer in a way that provides a facile method to tune the properties.

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