Cas 127405-70-3,4-[(E)-3-(3-{[2-(3,4-Dimethoxy-phenyl)-ethyl]-methyl-amino}-propylcarbamoyl)-propenyl]-benzoic acid methyl ester

127405-70-3

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Basic information

Product Name: 4-[(E)-3-(3-{[2-(3,4-Dimethoxy-phenyl)-ethyl]-methyl-amino}-propylcarbamoyl)-propenyl]-benzoic acid methyl ester
Synonyms: 4-[(E)-3-(3-{[2-(3,4-Dimethoxy-phenyl)-ethyl]-methyl-amino}-propylcarbamoyl)-propenyl]-benzoic acid methyl ester
CAS NO:127405-70-3
Molecular Formula:
Molecular Weight: 454.566
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: 4-[(E)-3-(3-{[2-(3,4-Dimethoxy-phenyl)-ethyl]-methyl-amino}-propylcarbamoyl)-propenyl]-benzoic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 4-[(E)-3-(3-{[2-(3,4-Dimethoxy-phenyl)-ethyl]-methyl-amino}-propylcarbamoyl)-propenyl]-benzoic acid methyl ester(127405-70-3)
EPA Substance Registry System: 4-[(E)-3-(3-{[2-(3,4-Dimethoxy-phenyl)-ethyl]-methyl-amino}-propylcarbamoyl)-propenyl]-benzoic acid methyl ester(127405-70-3)

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: 127405-70-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 127405-70-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,0 and 5 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 127405-70:
(8*1)+(7*2)+(6*7)+(5*4)+(4*0)+(3*5)+(2*7)+(1*0)=113
113 % 10 = 3
So 127405-70-3 is a valid CAS Registry Number.

127405-70-3Upstream product

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127405-70-3Relevant academic research and scientific papers

Synthesis and cardiovascular activity of phenylalkylamine derivatives. I. Potential specific bradycardic agents

Ozaki,Matsukura,Kabasawa,Ishibashi,Ikemori,Hamano,Minami

, p. 2735 - 2740 (2007/10/02)

A series of acyclic amide derivatives of N-(ω-aminoalkyl)-N-methylhomoveratrylamine was synthesized and evaluated for their bradycardic activity in isolated guinea pig right atria. Among these compounds, (E)-N-[3[N'-[2-(3,4-dimethoxyphenyl)ethyl]-N'-methy

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