Cas 1395060-91-9,5-cyano-6-imino-1-(4-methoxyphenyl)-4-phenyl-N-(pyridin-3-yl)-1,6-dihydro-pyridazine-3-carboxamide

1395060-91-9

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Basic information

Product Name: 5-cyano-6-imino-1-(4-methoxyphenyl)-4-phenyl-N-(pyridin-3-yl)-1,6-dihydro-pyridazine-3-carboxamide
Synonyms:
CAS NO:1395060-91-9
Molecular Formula:
Molecular Weight: 422.446
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: 5-cyano-6-imino-1-(4-methoxyphenyl)-4-phenyl-N-(pyridin-3-yl)-1,6-dihydro-pyridazine-3-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 5-cyano-6-imino-1-(4-methoxyphenyl)-4-phenyl-N-(pyridin-3-yl)-1,6-dihydro-pyridazine-3-carboxamide(1395060-91-9)
EPA Substance Registry System: 5-cyano-6-imino-1-(4-methoxyphenyl)-4-phenyl-N-(pyridin-3-yl)-1,6-dihydro-pyridazine-3-carboxamide(1395060-91-9)

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: 1395060-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1395060-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,5,0,6 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1395060-91:
(9*1)+(8*3)+(7*9)+(6*5)+(5*0)+(4*6)+(3*0)+(2*9)+(1*1)=169
169 % 10 = 9
So 1395060-91-9 is a valid CAS Registry Number.

1395060-91-9Upstream product

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1395060-91-9Relevant academic research and scientific papers

Activated anilide in heterocyclic synthesis: Synthesis of new hydrazo, dihydropyridazine, tetrahydropyridine, dihydropyridine and pyranopyridine derivatives

Hafiz, Ibrahim Saad Abdel,Ramiz, Mahmoud Mohamed Mahfouz,Elian, Mohamed Ahmed

, p. 647 - 655 (2012/08/27)

A series of new hydrazo, dihydropyridazine, tetrahydropyridine, dihydropyridine and pyranopyridine derivatives with known biological activity have been prepared through the reactions of 3-oxo-3-phenyl-N- (pyridine-3-yl) propanamide 3 and enaminonitrile 17

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