Cas 1575718-02-3,4-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-benzo[h]pyrazolo[3,4-b]quinolin-5,6-dione

1575718-02-3

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Basic information

Product Name: 4-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-benzo[h]pyrazolo[3,4-b]quinolin-5,6-dione
Synonyms: 4-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-benzo[h]pyrazolo[3,4-b]quinolin-5,6-dione
CAS NO:1575718-02-3
Molecular Formula:
Molecular Weight: 480.867
EINECS: N/A
Product Categories: N/A
Mol File: 1575718-02-3.mol
Article Data: 1

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-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-benzo[h]pyrazolo[3,4-b]quinolin-5,6-dione(CAS DataBase Reference)
NIST Chemistry Reference: 4-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-benzo[h]pyrazolo[3,4-b]quinolin-5,6-dione(1575718-02-3)
EPA Substance Registry System: 4-(4-chlorophenyl)-3-(4-nitrophenyl)-1H-benzo[h]pyrazolo[3,4-b]quinolin-5,6-dione(1575718-02-3)

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: 1575718-02-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1575718-02-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,5,7,1 and 8 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1575718-02:
(9*1)+(8*5)+(7*7)+(6*5)+(5*7)+(4*1)+(3*8)+(2*0)+(1*2)=193
193 % 10 = 3
So 1575718-02-3 is a valid CAS Registry Number.

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1575718-02-3Relevant articles and documents

Microwave induced three-component synthesis and antimycobacterial activity of benzopyrazolo[3,4-b]quinolindiones

Quiroga, Jairo,Diaz, Yurina,Bueno, Juan,Insuasty, Braulio,Abonia, Rodrigo,Ortiz, Alejandro,Nogueras, Manuel,Cobo, Justo

, p. 216 - 224 (2014/02/14)

Three series of novel 4-arylbenzo[h]pyrazolo[3,4-b]quinolin-5,6-diones 4, 7 and 9 have been efficiently obtained in good yields by three-component microwave assisted reaction between aminopyrazoles 1 or 6 (both 1-phenyl and 1-H substituted), 2-hydroxynaph

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