Cas 1392830-45-3,12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one

1392830-45-3

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Basic information

Product Name: 12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one
Synonyms: 12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one
CAS NO:1392830-45-3
Molecular Formula:
Molecular Weight: 459.547
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: 12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one(CAS DataBase Reference)
NIST Chemistry Reference: 12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one(1392830-45-3)
EPA Substance Registry System: 12-(dimethylamino)-1-phenyl-2,3-dihydro-1H-chromeno[3,4-j]imidazo[1,2-f]phenanthridin-15(16bH)-one(1392830-45-3)

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: 1392830-45-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1392830-45-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,2,8,3 and 0 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1392830-45:
(9*1)+(8*3)+(7*9)+(6*2)+(5*8)+(4*3)+(3*0)+(2*4)+(1*5)=173
173 % 10 = 3
So 1392830-45-3 is a valid CAS Registry Number.

1392830-45-3Upstream product

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1392830-45-3Relevant academic research and scientific papers

Synthesis of a coumarin/phenanthridine-fused heterocycle as a lockable colorimetric fluorescence molecular switch

Su, Shih-Hsun,Yang, Ding-Yah

, p. 253 - 263 (2012/07/03)

A coumarin/phenanthridine-fused heterocycle was synthesized via base-mediated annulation of N-alkylquinolinium salt and coumarin. Its potential to function as a lockable molecular switch by use of pH and redox chemistry as external stimuli was evaluated.

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