Cas 1133775-59-3,[3-(2,4-dichlorophenyl)-4-imino-1-(4-nitrophenyl)-1,4-dihydro-5H-pyrazolo[3,4-d]pyrimidin-5-yl]amine

1133775-59-3

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Basic information

Product Name: [3-(2,4-dichlorophenyl)-4-imino-1-(4-nitrophenyl)-1,4-dihydro-5H-pyrazolo[3,4-d]pyrimidin-5-yl]amine
Synonyms: [3-(2,4-dichlorophenyl)-4-imino-1-(4-nitrophenyl)-1,4-dihydro-5H-pyrazolo[3,4-d]pyrimidin-5-yl]amine
CAS NO:1133775-59-3
Molecular Formula:
Molecular Weight: 416.226
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: [3-(2,4-dichlorophenyl)-4-imino-1-(4-nitrophenyl)-1,4-dihydro-5H-pyrazolo[3,4-d]pyrimidin-5-yl]amine(CAS DataBase Reference)
NIST Chemistry Reference: [3-(2,4-dichlorophenyl)-4-imino-1-(4-nitrophenyl)-1,4-dihydro-5H-pyrazolo[3,4-d]pyrimidin-5-yl]amine(1133775-59-3)
EPA Substance Registry System: [3-(2,4-dichlorophenyl)-4-imino-1-(4-nitrophenyl)-1,4-dihydro-5H-pyrazolo[3,4-d]pyrimidin-5-yl]amine(1133775-59-3)

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: 1133775-59-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1133775-59-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,3,7,7 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1133775-59:
(9*1)+(8*1)+(7*3)+(6*3)+(5*7)+(4*7)+(3*5)+(2*5)+(1*9)=153
153 % 10 = 3
So 1133775-59-3 is a valid CAS Registry Number.

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1133775-59-3Relevant academic research and scientific papers

Synthesis and antimicrobial activity of some new pyrazole, fused pyrazolo[3,4-d]-pyrimidine and pyrazolo[4,3-e][1,2,4]-triazolo[1,5-c]pyrimidine derivatives

Abunada, Nada M.,Hassaneen, Hamdi M.,Kandile, Nadia G.,Miqdad, Omar A.

, p. 1501 - 1517 (2008/12/22)

Hydrazonyl bromides 2a,b reacted with active methylene compounds (dibenzoylmethane, acetylacetone, ethyl acetoacetate, phenacyl cyanide, acetoacetanilide, ethyl cyanoacetate, cyanoacetamide and malononitrile) to afford the corresponding 1,3,4,5-tetrasubst

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