Cas 1569352-23-3,6-bromo-N-(2-(cyclohexylamino)-1-(5-methoxy-2-((1-(3-nitrophenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-2-oxoethyl)-2-oxo-N-(p-tolyl)-2H-chromene-3-carboxamide

1569352-23-3

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Basic information

Product Name: 6-bromo-N-(2-(cyclohexylamino)-1-(5-methoxy-2-((1-(3-nitrophenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-2-oxoethyl)-2-oxo-N-(p-tolyl)-2H-chromene-3-carboxamide
Synonyms:
CAS NO:1569352-23-3
Molecular Formula:
Molecular Weight: 821.684
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: 6-bromo-N-(2-(cyclohexylamino)-1-(5-methoxy-2-((1-(3-nitrophenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-2-oxoethyl)-2-oxo-N-(p-tolyl)-2H-chromene-3-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 6-bromo-N-(2-(cyclohexylamino)-1-(5-methoxy-2-((1-(3-nitrophenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-2-oxoethyl)-2-oxo-N-(p-tolyl)-2H-chromene-3-carboxamide(1569352-23-3)
EPA Substance Registry System: 6-bromo-N-(2-(cyclohexylamino)-1-(5-methoxy-2-((1-(3-nitrophenyl)-1H-1,2,3-triazol-4-yl)methoxy)phenyl)-2-oxoethyl)-2-oxo-N-(p-tolyl)-2H-chromene-3-carboxamide(1569352-23-3)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1569352-23-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1569352-23-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,3,5 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1569352-23:
(9*1)+(8*5)+(7*6)+(6*9)+(5*3)+(4*5)+(3*2)+(2*2)+(1*3)=193
193 % 10 = 3
So 1569352-23-3 is a valid CAS Registry Number.

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1569352-23-3Relevant academic research and scientific papers

One-pot synthesis of coumarin-3-carboxamides containing a triazole ring via an isocyanide-based six-component reaction

Shaabani, Shabnam,Shaabani, Ahmad,Ng, Seik Weng

, p. 176 - 183 (2014/05/06)

A facile, efficient, and environmentally friendly approach has been developed for the diversity oriented synthesis of trifunctional coumarin-amide-triazole containing compounds. A wide variety of pharmacologically significant and structurally interesting compounds were synthesized via a one-pot, six-component, tandem Knoevenagel/Ugi/click reaction sequence from readily available starting materials in ethanol at room temperature in excellent overall yields. Substituents could be independently varied at five different positions.

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