Cas 1450728-68-3,(E)-N-((2-(1-(benzo[d][1,3]dioxol-5-yl)ethyl)naphthalen-1-yl)methylene)-4-methoxyaniline

1450728-68-3

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Basic information

Product Name: (E)-N-((2-(1-(benzo[d][1,3]dioxol-5-yl)ethyl)naphthalen-1-yl)methylene)-4-methoxyaniline
Synonyms: (E)-N-((2-(1-(benzo[d][1,3]dioxol-5-yl)ethyl)naphthalen-1-yl)methylene)-4-methoxyaniline
CAS NO:1450728-68-3
Molecular Formula:
Molecular Weight: 409.485
EINECS: N/A
Product Categories: N/A
Mol File: 1450728-68-3.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: (E)-N-((2-(1-(benzo[d][1,3]dioxol-5-yl)ethyl)naphthalen-1-yl)methylene)-4-methoxyaniline(CAS DataBase Reference)
NIST Chemistry Reference: (E)-N-((2-(1-(benzo[d][1,3]dioxol-5-yl)ethyl)naphthalen-1-yl)methylene)-4-methoxyaniline(1450728-68-3)
EPA Substance Registry System: (E)-N-((2-(1-(benzo[d][1,3]dioxol-5-yl)ethyl)naphthalen-1-yl)methylene)-4-methoxyaniline(1450728-68-3)

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: 1450728-68-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1450728-68-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,5,0,7,2 and 8 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1450728-68:
(9*1)+(8*4)+(7*5)+(6*0)+(5*7)+(4*2)+(3*8)+(2*6)+(1*8)=163
163 % 10 = 3
So 1450728-68-3 is a valid CAS Registry Number.

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1450728-68-3Relevant articles and documents

Aldimine-directed branched-selective hydroarylation of styrenes

Lee, Pin-Sheng,Yoshikai, Naohiko

supporting information, p. 1240 - 1244 (2013/03/13)

Branching out: A simple and inexpensive cobalt/triarylphosphine catalyst promotes aldimine-directed hydroarylation of styrene with high branched regioselectivity to afford 1,1-diarylethane derivatives in good yields under mild reaction conditions. The ortho-formyl group in the hydroarylation products is amenable to dehydrative cyclization, to give fused polycyclic aromatic hydrocarbons, as well as decarbonylative removal. Copyright

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