Cas 125422-61-9,2,5-diphenyl-7-carbethoxy-2,4,6,8-tetraaza <3.3.1>bicyclooct-5-ene-1,3-dione

125422-61-9

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Basic information

Product Name: 2,5-diphenyl-7-carbethoxy-2,4,6,8-tetraaza <3.3.1>bicyclooct-5-ene-1,3-dione
Synonyms: 2,5-diphenyl-7-carbethoxy-2,4,6,8-tetraaza <3.3.1>bicyclooct-5-ene-1,3-dione
CAS NO:125422-61-9
Molecular Formula:
Molecular Weight: 364.36
EINECS: N/A
Product Categories: N/A
Mol File: 125422-61-9.mol
Article Data: 1

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: 2,5-diphenyl-7-carbethoxy-2,4,6,8-tetraaza <3.3.1>bicyclooct-5-ene-1,3-dione(CAS DataBase Reference)
NIST Chemistry Reference: 2,5-diphenyl-7-carbethoxy-2,4,6,8-tetraaza <3.3.1>bicyclooct-5-ene-1,3-dione(125422-61-9)
EPA Substance Registry System: 2,5-diphenyl-7-carbethoxy-2,4,6,8-tetraaza <3.3.1>bicyclooct-5-ene-1,3-dione(125422-61-9)

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: 125422-61-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125422-61-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,4,2 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 125422-61:
(8*1)+(7*2)+(6*5)+(5*4)+(4*2)+(3*2)+(2*6)+(1*1)=99
99 % 10 = 9
So 125422-61-9 is a valid CAS Registry Number.

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125422-61-9Relevant articles and documents

DO OXAZOLES UNDERGO DIELS-ALDER REACTIONS WITH HETERODIENOPHILES ?

Hassner, Alfred,Fischer, Bilha

, p. 3535 - 3546 (2007/10/02)

5-Alkoxy and 2-alkoxyoxazoles wre shown to react with N=N, C=N or C=O dienophiles to form products that in most cases can be explained to result from a Diels-Alder addition, or by nucleophilic attack of the oxazole on the dienophile, followed by rearrangement.The products are triazolines, imidazolines or oxazolines respectively.Relative reactivities were established and mechanistic pathways discussed.

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