Cas 1449215-84-2,2-{[(6-ethyl-2-ethoxy-4-oxo-2H-chromen-3(4H)-ylidene)methyl]amino}benzenesulfonamide

1449215-84-2

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Basic information

Product Name: 2-{[(6-ethyl-2-ethoxy-4-oxo-2H-chromen-3(4H)-ylidene)methyl]amino}benzenesulfonamide
Synonyms: 2-{[(6-ethyl-2-ethoxy-4-oxo-2H-chromen-3(4H)-ylidene)methyl]amino}benzenesulfonamide
CAS NO:1449215-84-2
Molecular Formula:
Molecular Weight: 402.471
EINECS: N/A
Product Categories: N/A
Mol File: 1449215-84-2.mol
Article Data: 2

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: 2-{[(6-ethyl-2-ethoxy-4-oxo-2H-chromen-3(4H)-ylidene)methyl]amino}benzenesulfonamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-{[(6-ethyl-2-ethoxy-4-oxo-2H-chromen-3(4H)-ylidene)methyl]amino}benzenesulfonamide(1449215-84-2)
EPA Substance Registry System: 2-{[(6-ethyl-2-ethoxy-4-oxo-2H-chromen-3(4H)-ylidene)methyl]amino}benzenesulfonamide(1449215-84-2)

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: 1449215-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1449215-84-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,9,2,1 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1449215-84:
(9*1)+(8*4)+(7*4)+(6*9)+(5*2)+(4*1)+(3*5)+(2*8)+(1*4)=172
172 % 10 = 2
So 1449215-84-2 is a valid CAS Registry Number.

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1449215-84-2Relevant articles and documents

2-Alkoxy-3-(sulfonylarylaminomethylene)-chroman-4-ones as potent and selective inhibitors of ectonucleotidases

Al-Rashida, Mariya,Batool, Gazala,Sattar, Almas,Ejaz, Syeda Abida,Khan, Samiullah,Lecka, Joanna,Sévigny, Jean,Hameed, Abdul,Iqbal, Jamshed

, p. 484 - 494 (2016)

A facile method for the modulation of 2-alkoxy side chain of 3-formylchromone enamines has been exploited for the synthesis of a series of 2-alkoxy-3-(sulfonylarylaminomethylene)-chroman-4-ones. This modulation was achieved by simply changing the alcoholi

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