Cas 415915-01-4,1-[(4-methoxy-phenyl)-hydrazono]-9-oxo-1,2,3,4,9,10-hexahydro-acridine-4-carboxylic acid ethyl ester

415915-01-4

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Basic information

Product Name: 1-[(4-methoxy-phenyl)-hydrazono]-9-oxo-1,2,3,4,9,10-hexahydro-acridine-4-carboxylic acid ethyl ester
Synonyms:
CAS NO:415915-01-4
Molecular Formula:
Molecular Weight: 405.453
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-methoxy-phenyl)-hydrazono]-9-oxo-1,2,3,4,9,10-hexahydro-acridine-4-carboxylic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 1-[(4-methoxy-phenyl)-hydrazono]-9-oxo-1,2,3,4,9,10-hexahydro-acridine-4-carboxylic acid ethyl ester(415915-01-4)
EPA Substance Registry System: 1-[(4-methoxy-phenyl)-hydrazono]-9-oxo-1,2,3,4,9,10-hexahydro-acridine-4-carboxylic acid ethyl ester(415915-01-4)

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: 415915-01-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 415915-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,5,9,1 and 5 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 415915-01:
(8*4)+(7*1)+(6*5)+(5*9)+(4*1)+(3*5)+(2*0)+(1*1)=134
134 % 10 = 4
So 415915-01-4 is a valid CAS Registry Number.

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415915-01-4Relevant academic research and scientific papers

Synthesis and cytotoxicity of potential anticancer derivatives of pyrazolo[3,4,5-kl]acridine and indolo[2,3-a]acridine

Bu, Xianyong,Chen, Junjie,Deady, Leslie W,Denny, William A

, p. 175 - 181 (2002)

Pyrazolo[3,4,5-kl]acridines were prepared by reaction of ethyl 1,9-dioxo-1,2,3,4,9,10-hexahydroacridine-4-carboxylate (4) with hydrazine and its methyl and 2-(dimethylamino)ethyl derivatives, followed by aromatization of the intermediate products with 1,4

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