Cas 1620197-94-5,(Z)-4-((5-((4-oxonaphthalen-1(4H)-ylidene)(phenyl)methyl)naphthalen-1-yl)oxy)phthalonitrile

1620197-94-5

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Basic information

Product Name: (Z)-4-((5-((4-oxonaphthalen-1(4H)-ylidene)(phenyl)methyl)naphthalen-1-yl)oxy)phthalonitrile
Synonyms: (Z)-4-((5-((4-oxonaphthalen-1(4H)-ylidene)(phenyl)methyl)naphthalen-1-yl)oxy)phthalonitrile
CAS NO:1620197-94-5
Molecular Formula:
Molecular Weight: 500.556
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: (Z)-4-((5-((4-oxonaphthalen-1(4H)-ylidene)(phenyl)methyl)naphthalen-1-yl)oxy)phthalonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (Z)-4-((5-((4-oxonaphthalen-1(4H)-ylidene)(phenyl)methyl)naphthalen-1-yl)oxy)phthalonitrile(1620197-94-5)
EPA Substance Registry System: (Z)-4-((5-((4-oxonaphthalen-1(4H)-ylidene)(phenyl)methyl)naphthalen-1-yl)oxy)phthalonitrile(1620197-94-5)

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: 1620197-94-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1620197-94-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,1,9 and 7 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1620197-94:
(9*1)+(8*6)+(7*2)+(6*0)+(5*1)+(4*9)+(3*7)+(2*9)+(1*4)=155
155 % 10 = 5
So 1620197-94-5 is a valid CAS Registry Number.

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1620197-94-5Relevant academic research and scientific papers

Synthesis, photophysical and photochemical properties of metal-free and zinc(II) phthalocyanines bearing α-naphtholbenzein units

?z?e?meci, Mukaddes

, p. 16 - 21 (2014)

Synthesis of metal-free and zinc (II) phthalocyanine complexes bearing α-naphtholbenzein units was described. Precursor required for the preparation of phthalocyanine complexes was prepared by nucleophilic aromatic substitution reaction between 4-nitropht

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