Cas 88377-20-2,4-Acridinecarboxamide, 9-[[2-methoxy-4-[(methylsulfonyl)amino]phenyl]amino]-5-methyl-, monohydrochloride

88377-20-2

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Basic information

Product Name: 4-Acridinecarboxamide, 9-[[2-methoxy-4-[(methylsulfonyl)amino]phenyl]amino]-5-methyl-, monohydrochloride
Synonyms:
CAS NO:88377-20-2
Molecular Formula: C23H22N4O4S.ClH
Molecular Weight: 486.979
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: 4-Acridinecarboxamide, 9-[[2-methoxy-4-[(methylsulfonyl)amino]phenyl]amino]-5-methyl-, monohydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: 4-Acridinecarboxamide, 9-[[2-methoxy-4-[(methylsulfonyl)amino]phenyl]amino]-5-methyl-, monohydrochloride(88377-20-2)
EPA Substance Registry System: 4-Acridinecarboxamide, 9-[[2-methoxy-4-[(methylsulfonyl)amino]phenyl]amino]-5-methyl-, monohydrochloride(88377-20-2)

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: 88377-20-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 88377-20-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,3,7 and 7 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88377-20:
(7*8)+(6*8)+(5*3)+(4*7)+(3*7)+(2*2)+(1*0)=172
172 % 10 = 2
So 88377-20-2 is a valid CAS Registry Number.

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88377-20-2Relevant academic research and scientific papers

Potential antitumor agents. 40. Orally active 4,5-disubstituted derivatives of amsacrine

Denny,Atwell,Baguley

, p. 363 - 367 (2007/10/02)

The DNA-intercalating agent amsacrine is an effective drug for the treatment of human leukemias and lymphomas but has minimal solid tumor activity. As a first step in identifying analogues with a wider spectrum of activity, a comparison was made of the in

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