Cas 119877-53-1,ethyl 2,3,4,5,6-pentafluoro-α-<<(4-fluorophenyl)amino>methylene>-β-oxobenzenepropionate

119877-53-1

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Basic information

Product Name: ethyl 2,3,4,5,6-pentafluoro-α-<<(4-fluorophenyl)amino>methylene>-β-oxobenzenepropionate
Synonyms: ethyl 2,3,4,5,6-pentafluoro-α-<<(4-fluorophenyl)amino>methylene>-β-oxobenzenepropionate
CAS NO:119877-53-1
Molecular Formula:
Molecular Weight: 403.281
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: ethyl 2,3,4,5,6-pentafluoro-α-<<(4-fluorophenyl)amino>methylene>-β-oxobenzenepropionate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 2,3,4,5,6-pentafluoro-α-<<(4-fluorophenyl)amino>methylene>-β-oxobenzenepropionate(119877-53-1)
EPA Substance Registry System: ethyl 2,3,4,5,6-pentafluoro-α-<<(4-fluorophenyl)amino>methylene>-β-oxobenzenepropionate(119877-53-1)

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: 119877-53-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 119877-53-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,8,7 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 119877-53:
(8*1)+(7*1)+(6*9)+(5*8)+(4*7)+(3*7)+(2*5)+(1*3)=171
171 % 10 = 1
So 119877-53-1 is a valid CAS Registry Number.

119877-53-1Upstream product

119877-53-1Downstream Products

107564-03-4 5,6,7,8-Tetrafluoro-1-(4-fluoro-phenyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid ethyl ester

119877-53-1Relevant academic research and scientific papers

Synthesis of novel 5-fluoro analogues of norfloxacin and ciprofloxacin

Moran,Ziegler Jr.,Dunne,Kuck,Lin

, p. 1313 - 1318 (1989)

A series of polyfluoro-3-quinolonecarboxylic acids have been synthesized and their in vitro antibacterial activity evaluated. The desired 7-(substituted amino) derivatives were prepared from the 5,6,7,8-tetrafluoroquinolone acids. Conversely, amine displa

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