Cas 1443017-99-9,1-(3-((tert-butyldimethylsilyl)oxy)propyl)-5-(4-methoxyphenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one

1443017-99-9

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Basic information

Product Name: 1-(3-((tert-butyldimethylsilyl)oxy)propyl)-5-(4-methoxyphenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one
Synonyms: 1-(3-((tert-butyldimethylsilyl)oxy)propyl)-5-(4-methoxyphenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one
CAS NO:1443017-99-9
Molecular Formula:
Molecular Weight: 451.681
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: 1-(3-((tert-butyldimethylsilyl)oxy)propyl)-5-(4-methoxyphenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 1-(3-((tert-butyldimethylsilyl)oxy)propyl)-5-(4-methoxyphenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one(1443017-99-9)
EPA Substance Registry System: 1-(3-((tert-butyldimethylsilyl)oxy)propyl)-5-(4-methoxyphenyl)-2-phenyl-2,3-dihydropyridin-4(1H)-one(1443017-99-9)

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: 1443017-99-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1443017-99-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,3,0,1 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1443017-99:
(9*1)+(8*4)+(7*4)+(6*3)+(5*0)+(4*1)+(3*7)+(2*9)+(1*9)=139
139 % 10 = 9
So 1443017-99-9 is a valid CAS Registry Number.

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1443017-99-9Relevant academic research and scientific papers

Palladium-catalyzed direct C-H arylation of cyclic enaminones with aryl iodides

Yu, Yi-Yun,Bi, Lei,Georg, Gunda I.

, p. 6163 - 6169 (2013/07/26)

A ligand-free method for the Pd-catalyzed direct arylation of cyclic enaminones using aryl iodides was developed. This method can be applied to a wide range of cyclic enaminones and aryl iodides with excellent C5-regioselectivity. Using widely available aryl iodides, the generality of this transformation provides easy access to a variety of 3-arylpiperidine structural motifs.

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