Cas 129895-55-2,N-{2-[2-Hydroxy-3-(4-methoxy-phenoxy)-propylamino]-ethyl}-4-methanesulfonylamino-benzamide

129895-55-2

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Basic information

Product Name: N-{2-[2-Hydroxy-3-(4-methoxy-phenoxy)-propylamino]-ethyl}-4-methanesulfonylamino-benzamide
Synonyms:
CAS NO:129895-55-2
Molecular Formula:
Molecular Weight: 437.517
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: N-{2-[2-Hydroxy-3-(4-methoxy-phenoxy)-propylamino]-ethyl}-4-methanesulfonylamino-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{2-[2-Hydroxy-3-(4-methoxy-phenoxy)-propylamino]-ethyl}-4-methanesulfonylamino-benzamide(129895-55-2)
EPA Substance Registry System: N-{2-[2-Hydroxy-3-(4-methoxy-phenoxy)-propylamino]-ethyl}-4-methanesulfonylamino-benzamide(129895-55-2)

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: 129895-55-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 129895-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,9,8,9 and 5 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 129895-55:
(8*1)+(7*2)+(6*9)+(5*8)+(4*9)+(3*5)+(2*5)+(1*5)=182
182 % 10 = 2
So 129895-55-2 is a valid CAS Registry Number.

129895-55-2Upstream product

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129895-55-2Relevant academic research and scientific papers

Synthesis of novel (aryloxy)propanolamines and related compounds possessing both class II and class III antiarrhythmic activity

Lis,Morgan Jr.,Marisca,Gomez,Lind,Davey,Phillips,Sullivan

, p. 2883 - 2891 (2007/10/02)

Several (aryloxy)propanolamines and related compounds (i.e. 5-13, 16-18, 20-24, 27-33, 35, 37-39, 41, and 42) were synthesized and investigated for their class III electrophysiological activity and class II (β-blocking) effects with use of in vitro and in

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