Cas 1449697-63-5,(3R,5aS,6R,7aR,8aR,11R,13aR,13bS,14aR)-6-hydroxy-6-(2-indolyl) 5,13-dioxo-3,11-diphenylperhydrodioxazolo[3,2-b][3’,2’-j]-2,8-phenanthroline

1449697-63-5

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Basic information

Product Name: (3R,5aS,6R,7aR,8aR,11R,13aR,13bS,14aR)-6-hydroxy-6-(2-indolyl) 5,13-dioxo-3,11-diphenylperhydrodioxazolo[3,2-b][3’,2’-j]-2,8-phenanthroline
Synonyms: (3R,5aS,6R,7aR,8aR,11R,13aR,13bS,14aR)-6-hydroxy-6-(2-indolyl) 5,13-dioxo-3,11-diphenylperhydrodioxazolo[3,2-b][3’,2’-j]-2,8-phenanthroline
CAS NO:1449697-63-5
Molecular Formula:
Molecular Weight: 589.691
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: (3R,5aS,6R,7aR,8aR,11R,13aR,13bS,14aR)-6-hydroxy-6-(2-indolyl) 5,13-dioxo-3,11-diphenylperhydrodioxazolo[3,2-b][3’,2’-j]-2,8-phenanthroline(CAS DataBase Reference)
NIST Chemistry Reference: (3R,5aS,6R,7aR,8aR,11R,13aR,13bS,14aR)-6-hydroxy-6-(2-indolyl) 5,13-dioxo-3,11-diphenylperhydrodioxazolo[3,2-b][3’,2’-j]-2,8-phenanthroline(1449697-63-5)
EPA Substance Registry System: (3R,5aS,6R,7aR,8aR,11R,13aR,13bS,14aR)-6-hydroxy-6-(2-indolyl) 5,13-dioxo-3,11-diphenylperhydrodioxazolo[3,2-b][3’,2’-j]-2,8-phenanthroline(1449697-63-5)

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: 1449697-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449697-63-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,6,9 and 7 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1449697-63:
(9*1)+(8*4)+(7*4)+(6*9)+(5*6)+(4*9)+(3*7)+(2*6)+(1*3)=225
225 % 10 = 5
So 1449697-63-5 is a valid CAS Registry Number.

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1449697-63-5Relevant academic research and scientific papers

Unsaturated oxazolopiperidone lactams: An unexpected dominotype double conjugate addition-cyclization process

Amat, Mercedes,Llor, Nuria,Checa, Begona,Perez, Maria,Bosch, Joan

, p. 6 - 18 (2014/03/21)

Reactions of 2-acetylindole enolate with unsaturated oxazolopiperidones 3, 4 and 10 unexpectedly gives pentacyclic dilactams 6, 7 and 11, respectively, resulting from a domino-type process involving two successive conjugate additions and a final cyclization.

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