Cas 1589517-79-2,5-(1,2-dithiolan-3-yl)-1-(4-(3,4,5-trimethoxybenzyl)piperazin-1-yl)pentan-1-one

1589517-79-2

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Basic information

Product Name: 5-(1,2-dithiolan-3-yl)-1-(4-(3,4,5-trimethoxybenzyl)piperazin-1-yl)pentan-1-one
Synonyms: 5-(1,2-dithiolan-3-yl)-1-(4-(3,4,5-trimethoxybenzyl)piperazin-1-yl)pentan-1-one
CAS NO:1589517-79-2
Molecular Formula:
Molecular Weight: 454.655
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: 5-(1,2-dithiolan-3-yl)-1-(4-(3,4,5-trimethoxybenzyl)piperazin-1-yl)pentan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 5-(1,2-dithiolan-3-yl)-1-(4-(3,4,5-trimethoxybenzyl)piperazin-1-yl)pentan-1-one(1589517-79-2)
EPA Substance Registry System: 5-(1,2-dithiolan-3-yl)-1-(4-(3,4,5-trimethoxybenzyl)piperazin-1-yl)pentan-1-one(1589517-79-2)

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: 1589517-79-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1589517-79-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,9,5,1 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1589517-79:
(9*1)+(8*5)+(7*8)+(6*9)+(5*5)+(4*1)+(3*7)+(2*7)+(1*9)=232
232 % 10 = 2
So 1589517-79-2 is a valid CAS Registry Number.

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1589517-79-2Relevant academic research and scientific papers

Development of cholinesterase inhibitors using (a)-lipoic acid-benzyl piperazine hybrid molecules

Kim, Beom-Cheol,Lee, Seung-Hwan,Jang, Mi,Shon, Min Young,Park, Jeong Ho

, p. 3322 - 3326 (2014/01/06)

A series of hybrid molecules between (a)-lipoic acid (ALA) and benzyl piperazines were synthesized and their in vitro cholinesterase [acetylcholinesterase (AChE) and butyrylcholinesterase (BuChE)] inhibitory activities were evaluated. Even though the pare

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