Cas 476350-39-7,<i>N</i>-[3-(6-amino-purin-9-yl)-propyl]-4-methyl-<i>N</i>-(6-methyl-phenanthridin-8-yl)-benzenesulfonamide

476350-39-7

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Basic information

Product Name: N-[3-(6-amino-purin-9-yl)-propyl]-4-methyl-N-(6-methyl-phenanthridin-8-yl)-benzenesulfonamide
Synonyms: N-[3-(6-amino-purin-9-yl)-propyl]-4-methyl-N-(6-methyl-phenanthridin-8-yl)-benzenesulfonamide
CAS NO:476350-39-7
Molecular Formula:
Molecular Weight: 537.645
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-[3-(6-amino-purin-9-yl)-propyl]-4-methyl-N-(6-methyl-phenanthridin-8-yl)-benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[3-(6-amino-purin-9-yl)-propyl]-4-methyl-N-(6-methyl-phenanthridin-8-yl)-benzenesulfonamide(476350-39-7)
EPA Substance Registry System: N-[3-(6-amino-purin-9-yl)-propyl]-4-methyl-N-(6-methyl-phenanthridin-8-yl)-benzenesulfonamide(476350-39-7)

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: 476350-39-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 476350-39-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,6,3,5 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 476350-39:
(8*4)+(7*7)+(6*6)+(5*3)+(4*5)+(3*0)+(2*3)+(1*9)=167
167 % 10 = 7
So 476350-39-7 is a valid CAS Registry Number.

476350-39-7Upstream product

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476350-39-7Relevant academic research and scientific papers

Interactions of novel phenanthridinium-nucleobase conjugates with complementary and non-complementary nucleotides in aqueous media

Tumir, Lidija-Marija,Piantanida, Ivo,Novak, Predrag,Zinic, Mladen

, p. 599 - 607 (2007/10/03)

A series of novel phenanthridine-nucleobase conjugates were prepared and studied by spectroscopic methods. An analysis of 1H NMR, UV-Vis and fluorescence spectra in aqueous media revealed intramolecular aromatic stacking interactions between th

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