Cas 1301714-79-3,N-butyl-2-(2-(2-(butylamino)-2-oxoethyl)-4-methoxyphenyl)-7-methoxy-4-methyl-1-naphthamide

1301714-79-3

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Basic information

Product Name: N-butyl-2-(2-(2-(butylamino)-2-oxoethyl)-4-methoxyphenyl)-7-methoxy-4-methyl-1-naphthamide
Synonyms: N-butyl-2-(2-(2-(butylamino)-2-oxoethyl)-4-methoxyphenyl)-7-methoxy-4-methyl-1-naphthamide
CAS NO:1301714-79-3
Molecular Formula:
Molecular Weight: 490.643
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: N-butyl-2-(2-(2-(butylamino)-2-oxoethyl)-4-methoxyphenyl)-7-methoxy-4-methyl-1-naphthamide(CAS DataBase Reference)
NIST Chemistry Reference: N-butyl-2-(2-(2-(butylamino)-2-oxoethyl)-4-methoxyphenyl)-7-methoxy-4-methyl-1-naphthamide(1301714-79-3)
EPA Substance Registry System: N-butyl-2-(2-(2-(butylamino)-2-oxoethyl)-4-methoxyphenyl)-7-methoxy-4-methyl-1-naphthamide(1301714-79-3)

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: 1301714-79-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1301714-79-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,1,7,1 and 4 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1301714-79:
(9*1)+(8*3)+(7*0)+(6*1)+(5*7)+(4*1)+(3*4)+(2*7)+(1*9)=113
113 % 10 = 3
So 1301714-79-3 is a valid CAS Registry Number.

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1301714-79-3Relevant academic research and scientific papers

Synthesis of 2-phenylnaphthalenes through gold-catalyzed dimerization via a highly selective carbon nucleophile pathway

Wang, Sinan,Zhang, Lei,Ding, Xiao,Zhou, Yu,Wang, Jinfang,Jiang, Hualiang,Liu, Hong

, p. 4514 - 4521 (2011/06/27)

A protocol for the facile synthesis of 2-phenylnaphthalene has been developed. The benzyl carbon acts as a nucleophilic center in the presence of the amide nitrogen and acetate oxygen, affording the selective formation of a naphthalene scaffold through th

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