Cas 89767-23-7,1,4,7,10-Tetraethyl-octahydro-1,3a,4,6a,7,9a,10,12a-octaaza-3b,6b,9b,12b-tetraphospha-tetracyclopenta[a,c,e,g]cyclooctene

89767-23-7

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Product Name: 1,4,7,10-Tetraethyl-octahydro-1,3a,4,6a,7,9a,10,12a-octaaza-3b,6b,9b,12b-tetraphospha-tetracyclopenta[a,c,e,g]cyclooctene
Synonyms: 1,4,7,10-Tetraethyl-octahydro-1,3a,4,6a,7,9a,10,12a-octaaza-3b,6b,9b,12b-tetraphospha-tetracyclopenta[a,c,e,g]cyclooctene
CAS NO:89767-23-7
Molecular Formula:
Molecular Weight: 464.41
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: 1,4,7,10-Tetraethyl-octahydro-1,3a,4,6a,7,9a,10,12a-octaaza-3b,6b,9b,12b-tetraphospha-tetracyclopenta[a,c,e,g]cyclooctene(CAS DataBase Reference)
NIST Chemistry Reference: 1,4,7,10-Tetraethyl-octahydro-1,3a,4,6a,7,9a,10,12a-octaaza-3b,6b,9b,12b-tetraphospha-tetracyclopenta[a,c,e,g]cyclooctene(89767-23-7)
EPA Substance Registry System: 1,4,7,10-Tetraethyl-octahydro-1,3a,4,6a,7,9a,10,12a-octaaza-3b,6b,9b,12b-tetraphospha-tetracyclopenta[a,c,e,g]cyclooctene(89767-23-7)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 89767-23-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89767-23-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,7,6 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89767-23:
(7*8)+(6*9)+(5*7)+(4*6)+(3*7)+(2*2)+(1*3)=197
197 % 10 = 7
So 89767-23-7 is a valid CAS Registry Number.

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89767-23-7Relevant academic research and scientific papers

Cyclotetra((λ3-phosphazanes) derivant de diamines-1,2. Precurseurs de composes du phosphore dicoordonne

Malavaud, Christian,N'Gando M'Pondo, Teophile,Lopez, Lucien,Barrans, Jean,Legros, Jean-Pierre

, p. 43 - 50 (2007/10/02)

Cyclotetraphosphazanes 2 and 5 obtained from 1,2-diamines are 1,3,2-diazaphosphole oligomers leading to the monomeric form by either thermal equilibrium or by complexing with boron trifluoride.The dicoordinated form stabilized by an orthophenylene ring could explain the reactivity of 4,5-benzo 1,3,2-diazaphosphole 3 with compounds having a mobile hydrogen; these reactions were a 1.2 type addition while butanol led to a 1.1 type addition with complexed 1,3,2-diazaphospholes 4 and 8.

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