Cas 125578-46-3,1-Oxo-1,2-dihydro-6H-pyrrolo[3,2,1-de]acridine-2-carboxylic acid (2,6-difluoro-phenyl)-amide

125578-46-3

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Basic information

Product Name: 1-Oxo-1,2-dihydro-6H-pyrrolo[3,2,1-de]acridine-2-carboxylic acid (2,6-difluoro-phenyl)-amide
Synonyms:
CAS NO:125578-46-3
Molecular Formula:
Molecular Weight: 376.362
EINECS: N/A
Product Categories: N/A
Mol File: 125578-46-3.mol
Article Data: 1

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: 1-Oxo-1,2-dihydro-6H-pyrrolo[3,2,1-de]acridine-2-carboxylic acid (2,6-difluoro-phenyl)-amide(CAS DataBase Reference)
NIST Chemistry Reference: 1-Oxo-1,2-dihydro-6H-pyrrolo[3,2,1-de]acridine-2-carboxylic acid (2,6-difluoro-phenyl)-amide(125578-46-3)
EPA Substance Registry System: 1-Oxo-1,2-dihydro-6H-pyrrolo[3,2,1-de]acridine-2-carboxylic acid (2,6-difluoro-phenyl)-amide(125578-46-3)

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: 125578-46-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 125578-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,5,5,7 and 8 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 125578-46:
(8*1)+(7*2)+(6*5)+(5*5)+(4*7)+(3*8)+(2*4)+(1*6)=143
143 % 10 = 3
So 125578-46-3 is a valid CAS Registry Number.

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125578-46-3Relevant articles and documents

1,2-Dihydro-1-oxopyrrolophenothiazine-2-carboxamides and Congeners, Dual Cyclooxygenase/5-Lipoxygenase Inhibitors with Antiinflammatory Activity

Mylari, Banavara L.,Carty, Thomas J.,Moore, Peter F.,Zembrowski, William J.

, p. 2019 - 2024 (2007/10/02)

A series of 1,2-dihydro-1-oxopyrrolophenothiazine, 1,2-dihydro-1-oxopyrrolophenoxazine, and 1,2-dihydro-1-oxopyrroloacridine-2-carboxamides were prepared by reaction of 1,2-dihydro-1-oxopyrrolophenothiazine or other

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