Cas 1620197-73-0,1-((furan-2-yl)carbonyl)-3-(5-chloro-2-hydroxyphenyl)-5-p-tolyl-4,5-dihydro-1H-pyrazole

1620197-73-0

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Basic information

Product Name: 1-((furan-2-yl)carbonyl)-3-(5-chloro-2-hydroxyphenyl)-5-p-tolyl-4,5-dihydro-1H-pyrazole
Synonyms: 1-((furan-2-yl)carbonyl)-3-(5-chloro-2-hydroxyphenyl)-5-p-tolyl-4,5-dihydro-1H-pyrazole
CAS NO:1620197-73-0
Molecular Formula:
Molecular Weight: 380.831
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: 1-((furan-2-yl)carbonyl)-3-(5-chloro-2-hydroxyphenyl)-5-p-tolyl-4,5-dihydro-1H-pyrazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-((furan-2-yl)carbonyl)-3-(5-chloro-2-hydroxyphenyl)-5-p-tolyl-4,5-dihydro-1H-pyrazole(1620197-73-0)
EPA Substance Registry System: 1-((furan-2-yl)carbonyl)-3-(5-chloro-2-hydroxyphenyl)-5-p-tolyl-4,5-dihydro-1H-pyrazole(1620197-73-0)

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: 1620197-73-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1620197-73-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,2,0,1,9 and 7 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1620197-73:
(9*1)+(8*6)+(7*2)+(6*0)+(5*1)+(4*9)+(3*7)+(2*7)+(1*3)=150
150 % 10 = 0
So 1620197-73-0 is a valid CAS Registry Number.

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1620197-73-0Relevant academic research and scientific papers

Synthesis of some novel hydrazone and 2-pyrazoline derivatives: Monoamine oxidase inhibitory activities and docking studies

Evranos-Aks?z, Begüm,Yabano?lu-?ift?i, Samiye,U?ar, Gülberk,Yelek?i, Kemal,Ertan, Rahmiye

, p. 3278 - 3284 (2014/07/22)

A novel series of 2-pyrazoline and hydrazone derivatives were synthesized and investigated for their human monoamine oxidase (hMAO) inhibitory activity. All compounds inhibited the hMAO isoforms (MAO-A or MAO-B) competitively and reversibly. With the exce

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