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C15H15Cl5N3O2P3 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

210972-45-5

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210972-45-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 210972-45-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,0,9,7 and 2 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 210972-45:
(8*2)+(7*1)+(6*0)+(5*9)+(4*7)+(3*2)+(2*4)+(1*5)=115
115 % 10 = 5
So 210972-45-5 is a valid CAS Registry Number.

210972-45-5Upstream product

210972-45-5Downstream Products

210972-45-5Relevant academic research and scientific papers

Interfacial synthesis of bisphenol A tetrachlorocyclotriphosphazene from bisphenol A and hexachlorocyclotriphosphazene

Thompson, Tiffany N.,Ramos-Hunter, Susan,Robertson, Jasmine,Arnett, Natalie Y.

supporting information, p. 5311 - 5313 (2013/09/12)

The effect of solvent purity on the synthesis and yield of bisphenol A tetrachlorocyclotriphosphazene (BATCCP) has not been described in the literature. The purpose of this research was to synthesize BATCCP hybrid monomers and to evaluate the effect of solvent purity on the BATCCP production. BATCCP monomers were prepared by an interfacial procedure in a water/toluene system as a function of time with the assistance of a phase transfer catalyst, tetraoctylammonium bromide. 1H and 31P NMR confirmed the production of BATCCP monomer by the appearance of chemical shifts at 7.18 and 5.35 ppm in the 1H NMR and 23.4 and 13.9 ppm in the 31P NMR, respectively. Distillation of the toluene, not suggested in previous reports of HCCP hybrid synthesis, resulted in an improvement of actual % yield to 40% and stability of the product throughout the 1440 min reaction as confirmed by MALDI, compared with an 11% actual yield at 15 min, decaying to 2% over a 1440 min reaction when the synthesis was performed with 'anhydrous toluene' as provided commercially without further distillation.

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