Cas 96567-08-7,4,15-bis(4-ethoxyphenyl)-8,10,19,21-tetramethyl-2,4,6,8,10,13,15,17,19,21-decaazahexacyclo<10.10.0.01.18.02.6.07.12.013.17>docosan-3,5,9,11,14,16,20,22-octaone

96567-08-7

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Basic information

Product Name: 4,15-bis(4-ethoxyphenyl)-8,10,19,21-tetramethyl-2,4,6,8,10,13,15,17,19,21-decaazahexacyclo<10.10.0.0^1.18.0^2.6.0^7.12.0^13.17>docosan-3,5,9,11,14,16,20,22-octaone
Synonyms:
CAS NO:96567-08-7
Molecular Formula:
Molecular Weight: 716.667
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4,15-bis(4-ethoxyphenyl)-8,10,19,21-tetramethyl-2,4,6,8,10,13,15,17,19,21-decaazahexacyclo<10.10.0.0^1.18.0^2.6.0^7.12.0^13.17>docosan-3,5,9,11,14,16,20,22-octaone(CAS DataBase Reference)
NIST Chemistry Reference: 4,15-bis(4-ethoxyphenyl)-8,10,19,21-tetramethyl-2,4,6,8,10,13,15,17,19,21-decaazahexacyclo<10.10.0.0^1.18.0^2.6.0^7.12.0^13.17>docosan-3,5,9,11,14,16,20,22-octaone(96567-08-7)
EPA Substance Registry System: 4,15-bis(4-ethoxyphenyl)-8,10,19,21-tetramethyl-2,4,6,8,10,13,15,17,19,21-decaazahexacyclo<10.10.0.0^1.18.0^2.6.0^7.12.0^13.17>docosan-3,5,9,11,14,16,20,22-octaone(96567-08-7)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 96567-08-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 96567-08-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,6,5,6 and 7 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 96567-08:
(7*9)+(6*6)+(5*5)+(4*6)+(3*7)+(2*0)+(1*8)=177
177 % 10 = 7
So 96567-08-7 is a valid CAS Registry Number.

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96567-08-7Relevant academic research and scientific papers

Reactions of Uracils, 5. Bridged 1,2,5,6-Tetrazocanes with Uracil and Urazole Bridges by Dimerization of 5-(1,2,4-Triazolidin-1-yl)uracils

Wamhoff, Heinrich,Wald, Klemens,Kirfel, Armin,Farkas, Lajos,Samimi, Nabi,Will, Georg

, p. 436 - 443 (2007/10/02)

Upon N-bromosuccinimide oxidation 5-(1,2,4-triazolidin-1-yl)uracils 3a-d, easily accessible by insertion of the 4-R-TAD 1a-d to 1,3-dimethyluracil (2), react with radical head-to-tail dimerization to give the novel bridged 1,2,5,6-tetrazocanes 4a-d in hig

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