Cas 1195786-16-3,4-(3-(pyrrol-1-yl)benzyl)-N-(2-ethoxyphenyl)piperazine-1-carboxamide

1195786-16-3

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Basic information

Product Name: 4-(3-(pyrrol-1-yl)benzyl)-N-(2-ethoxyphenyl)piperazine-1-carboxamide
Synonyms: 4-(3-(pyrrol-1-yl)benzyl)-N-(2-ethoxyphenyl)piperazine-1-carboxamide
CAS NO:1195786-16-3
Molecular Formula:
Molecular Weight: 404.512
EINECS: N/A
Product Categories: N/A
Mol File: 1195786-16-3.mol
Article Data: 1

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-(3-(pyrrol-1-yl)benzyl)-N-(2-ethoxyphenyl)piperazine-1-carboxamide(CAS DataBase Reference)
NIST Chemistry Reference: 4-(3-(pyrrol-1-yl)benzyl)-N-(2-ethoxyphenyl)piperazine-1-carboxamide(1195786-16-3)
EPA Substance Registry System: 4-(3-(pyrrol-1-yl)benzyl)-N-(2-ethoxyphenyl)piperazine-1-carboxamide(1195786-16-3)

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: 1195786-16-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1195786-16-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,5,7,8 and 6 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1195786-16:
(9*1)+(8*1)+(7*9)+(6*5)+(5*7)+(4*8)+(3*6)+(2*1)+(1*6)=203
203 % 10 = 3
So 1195786-16-3 is a valid CAS Registry Number.

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1195786-16-3Relevant articles and documents

A multistep continuous-flow system for rapid on-demand synthesis of receptor ligands

Petersen, Trine P.,Ritzen, Andreas,Ulven, Trond

, p. 5134 - 5137 (2009)

A multistep continuous-flow system for synthesis of receptor ligands by assembly of three variable building blocks in a single unbroken flow is described. The sequence consists of three reactions and two scavenger steps, where a Cbz-protected diamine is reacted with an isocyanate, deprotected, and reacted further with an alkylating agent.

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