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78902-28-0

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78902-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78902-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,9,0 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 78902-28:
(7*7)+(6*8)+(5*9)+(4*0)+(3*2)+(2*2)+(1*8)=160
160 % 10 = 0
So 78902-28-0 is a valid CAS Registry Number.

78902-28-0Downstream Products

78902-28-0Relevant academic research and scientific papers

STUDIES OF THE 1,3,5,2,4,6-TRIOXATRIPHOSPHORINANE RING SYSTEM

Quin, Louis D.,Ionkin, Alexey S.

, p. 205 - 214 (2007/10/02)

Phosphorodichloridites with sterically demanding O-aryl groups are known to undergo controlled partial hydrolysis to give 1,3,5,2,4,6-trioxatriphosphorinane derivatives, but the O-(1-adamantyl) and O-neopentyl groups failed to provide control of the hydro

Thermal Retro-Trimerization of Some 1,3,5,2,4,6-Trioxatriphosphorinanes to Phosphenites

Quin, Louis D.,Ionkin, Alexey S.

, p. 5186 - 5189 (2007/10/02)

Pyrolysis in a packed tube of the vapor from three 2,4,6-tris(aryloxy)-1,3,5,2,4,6-trioxatriphosphorinanes was performed at 300-350 deg C and 1E-6 mm; the product was collected on a cold finger chilled by liquid nitrogen.The cracking of the trimer was complete, and the product at -195 deg C appeared to consist only of the monomeric aryl phosphenite, ArOP=O.On warming, dimerization occured, later followed by trimer formation.The weak 31P NMR signal for the phosphenite (about δ 238 for three O-aryl derivatives) persisted in the solution for several weeks if water was rigorously excluded.Treatment of the phosphenite with water or alcohols at -195 deg C gave a mixture of products; the major product (ArO-PH(O)OH) came from addition of the nucleophile to the P=O bond, but significant amounts (10-20percent) of dialkyl H-phosphonates (HP(O)(OR)2) were present, apparently from displacement of the O-aryl substituent of the phosphenite, followed by addition to the double bond.

Experiments on the Generation of 2-Coordinate Phosphoryl Species by Fragmentation of 7-Phosphanorbornene and 3-Phospholene Derivatives

Quin, Louis D.,Jankowski, Stefan,Rudzinski, Juliusz,Sommese, Anthony G.,Wu, Xiao-Ping

, p. 6212 - 6216 (2007/10/02)

2,6-Di-tert-butyl-4-methylphenyl phosphenite (ArOP=O) was released into the gas phase on heating a neat sample of a 7-phosphanorbornene derivative 6 bearing this aryloxy substituent at 300 deg C (0.01 mm).Attempts to prepare 1-adamantyl phosphenite simila

Synthesis and Structure of 2,4-Bis(2,6-di-tert-butyl-4-methylphenoxy)-1,3,2,4-dioxadiphosphetane. An Aryl Phosphenite Dimer

Chasar, Dwight W.,Fackler, John P.,Komoroski, Richard A.,Kroenke, William J.,Mazany, Anthony M.

, p. 5690 - 5693 (2007/10/02)

When 2,4,6-tris(2,6-di-tert-butyl-4-methylphenoxy)-1,3,5,2,4,6-trioxatriphosphorinane (1a) is sublimed at 220 deg C under vacuum, a new heterocycle, a 1,3,2,4-dioxadiphosphetane (3), is formed.This molecule can be considered a dimer of the aryl phosphenit

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