Cas 1427697-24-2,2-(3-((3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylamino)-2-hydroxypropylamino)quinolin-4(1H)-one

1427697-24-2

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Basic information

Product Name: 2-(3-((3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylamino)-2-hydroxypropylamino)quinolin-4(1H)-one
Synonyms: 2-(3-((3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylamino)-2-hydroxypropylamino)quinolin-4(1H)-one
CAS NO:1427697-24-2
Molecular Formula:
Molecular Weight: 483.545
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: 2-(3-((3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylamino)-2-hydroxypropylamino)quinolin-4(1H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(3-((3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylamino)-2-hydroxypropylamino)quinolin-4(1H)-one(1427697-24-2)
EPA Substance Registry System: 2-(3-((3-(4-fluorophenyl)-1-phenyl-1H-pyrazol-4-yl)methylamino)-2-hydroxypropylamino)quinolin-4(1H)-one(1427697-24-2)

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: 1427697-24-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1427697-24-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,6,9 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1427697-24:
(9*1)+(8*4)+(7*2)+(6*7)+(5*6)+(4*9)+(3*7)+(2*2)+(1*4)=192
192 % 10 = 2
So 1427697-24-2 is a valid CAS Registry Number.

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1427697-24-2Relevant academic research and scientific papers

Synthesis and antibacterial activity of new diaryldiamines

Samrin, Farhana,Sharma, Akash,Khan, Inshad Ali,Puri, Sadhna

, p. 1391 - 1397 (2013/02/22)

Several new quinolines and quinazolines (4, 10, 13) have been synthesized from cheap and readily available chemicals through a series of simple chemical transformations. Most of the synthesized compounds have been evaluated for antibacterial activity against Gram positive and Gram negative strains. Some of the synthesized compounds displayed interesting activity but not very promising for further development.

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