Cas 138286-70-1,Benzamide, N-[[4-(2-methoxyphenyl)-2-piperazinyl]methyl]-4-[(methylsulfonyl)amino]- , monohydrochloride

138286-70-1

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Basic information

Product Name: Benzamide, N-[[4-(2-methoxyphenyl)-2-piperazinyl]methyl]-4-[(methylsulfonyl)amino]- , monohydrochloride
Synonyms:
CAS NO:138286-70-1
Molecular Formula: C20H26N4O4S.ClH
Molecular Weight: 454.978
EINECS: N/A
Product Categories: N/A
Mol File: 138286-70-1.mol

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: Benzamide, N-[[4-(2-methoxyphenyl)-2-piperazinyl]methyl]-4-[(methylsulfonyl)amino]- , monohydrochloride(CAS DataBase Reference)
NIST Chemistry Reference: Benzamide, N-[[4-(2-methoxyphenyl)-2-piperazinyl]methyl]-4-[(methylsulfonyl)amino]- , monohydrochloride(138286-70-1)
EPA Substance Registry System: Benzamide, N-[[4-(2-methoxyphenyl)-2-piperazinyl]methyl]-4-[(methylsulfonyl)amino]- , monohydrochloride(138286-70-1)

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: 138286-70-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 138286-70-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,2,8 and 6 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 138286-70:
(8*1)+(7*3)+(6*8)+(5*2)+(4*8)+(3*6)+(2*7)+(1*0)=151
151 % 10 = 1
So 138286-70-1 is a valid CAS Registry Number.

138286-70-1Upstream product

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138286-70-1Relevant academic research and scientific papers

Synthesis, cardiac electrophysiology, and β-blocking activity of novel arylpiperazines with potential as class II/III antiarrhythmic agents

Phillips,Morgan Jr.,Lumma Jr.,Gomez,Lind,Lis,Argentieri,Sullivan

, p. 743 - 750 (2007/10/02)

A series of novel arylpiperazines have been prepared in an attempt to incorporate both class II (β-receptor blocking) and class III antiarrhythmic properties in a single molecule. The key step in the preparation of the new compounds involves a regioselect

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