Cas 1369423-69-7,11-(4-chlorophenyl)-3-(tetrahydro-2H-pyran-2-yl)benzo[f]pyridazino[4,5-b][1,4]oxazepine-4,10(3H,11H)-dione

1369423-69-7

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Basic information

Product Name: 11-(4-chlorophenyl)-3-(tetrahydro-2H-pyran-2-yl)benzo[f]pyridazino[4,5-b][1,4]oxazepine-4,10(3H,11H)-dione
Synonyms: 11-(4-chlorophenyl)-3-(tetrahydro-2H-pyran-2-yl)benzo[f]pyridazino[4,5-b][1,4]oxazepine-4,10(3H,11H)-dione
CAS NO:1369423-69-7
Molecular Formula:
Molecular Weight: 423.856
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: 11-(4-chlorophenyl)-3-(tetrahydro-2H-pyran-2-yl)benzo[f]pyridazino[4,5-b][1,4]oxazepine-4,10(3H,11H)-dione(CAS DataBase Reference)
NIST Chemistry Reference: 11-(4-chlorophenyl)-3-(tetrahydro-2H-pyran-2-yl)benzo[f]pyridazino[4,5-b][1,4]oxazepine-4,10(3H,11H)-dione(1369423-69-7)
EPA Substance Registry System: 11-(4-chlorophenyl)-3-(tetrahydro-2H-pyran-2-yl)benzo[f]pyridazino[4,5-b][1,4]oxazepine-4,10(3H,11H)-dione(1369423-69-7)

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: 1369423-69-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1369423-69-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,9,4,2 and 3 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1369423-69:
(9*1)+(8*3)+(7*6)+(6*9)+(5*4)+(4*2)+(3*3)+(2*6)+(1*9)=187
187 % 10 = 7
So 1369423-69-7 is a valid CAS Registry Number.

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1369423-69-7Relevant academic research and scientific papers

One-pot synthesis of fused pyridazino[4,5- b ][1,4]oxazepine-diones via smiles rearrangement

Liu, Yanli,Ma, Ying,Zhan, Chunjing,Huang, Aiping,Ma, Chen

, p. 255 - 258 (2012)

Fused pyridazino[4,5-b][1,4]oxazepine-diones were easily obtained in moderate to excellent yields via Smiles rearrangement. The synthetic approach is supported by a one-pot coupling-Smiles rearrangement-cyclization process. This process has potential appl

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