Cas 1357598-08-3,N-(5-(2-oxo-2H-naphtho[1,2-b][1,4]oxazin-3-yl)-1,3,4-oxadiazol-2-yl)benzamide

1357598-08-3

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Basic information

Product Name: N-(5-(2-oxo-2H-naphtho[1,2-b][1,4]oxazin-3-yl)-1,3,4-oxadiazol-2-yl)benzamide
Synonyms: N-(5-(2-oxo-2H-naphtho[1,2-b][1,4]oxazin-3-yl)-1,3,4-oxadiazol-2-yl)benzamide
CAS NO:1357598-08-3
Molecular Formula:
Molecular Weight: 384.351
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: N-(5-(2-oxo-2H-naphtho[1,2-b][1,4]oxazin-3-yl)-1,3,4-oxadiazol-2-yl)benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-(5-(2-oxo-2H-naphtho[1,2-b][1,4]oxazin-3-yl)-1,3,4-oxadiazol-2-yl)benzamide(1357598-08-3)
EPA Substance Registry System: N-(5-(2-oxo-2H-naphtho[1,2-b][1,4]oxazin-3-yl)-1,3,4-oxadiazol-2-yl)benzamide(1357598-08-3)

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: 1357598-08-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357598-08-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,5,9 and 8 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1357598-08:
(9*1)+(8*3)+(7*5)+(6*7)+(5*5)+(4*9)+(3*8)+(2*0)+(1*8)=203
203 % 10 = 3
So 1357598-08-3 is a valid CAS Registry Number.

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1357598-08-3Relevant academic research and scientific papers

Synthesis and antitumor evaluation of some new 1,3,4-oxadiazole-based heterocycles

Bondock, Samir,Adel, Shymaa,Etman, Hassan A.,Badria, Farid A.

experimental part, p. 192 - 199 (2012/03/26)

The synthetic strategies and characterization of some novel 1,3,4-oxadiazole derivatives carrying different pharmacophores and heterocyclic rings that are relevant to potential antitumor and cytotoxic activities are described. The antitumor activities of

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