Cas 19072-23-2,β-Propylamino-zimtsaeure-ethylester

19072-23-2

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Basic information

Product Name: β-Propylamino-zimtsaeure-ethylester
Synonyms: β-Propylamino-zimtsaeure-ethylester
CAS NO:19072-23-2
Molecular Formula:
Molecular Weight: 233.31
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: β-Propylamino-zimtsaeure-ethylester(CAS DataBase Reference)
NIST Chemistry Reference: β-Propylamino-zimtsaeure-ethylester(19072-23-2)
EPA Substance Registry System: β-Propylamino-zimtsaeure-ethylester(19072-23-2)

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: 19072-23-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 19072-23-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,0,7 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 19072-23:
(7*1)+(6*9)+(5*0)+(4*7)+(3*2)+(2*2)+(1*3)=102
102 % 10 = 2
So 19072-23-2 is a valid CAS Registry Number.

19072-23-2Upstream product

19072-23-2Downstream Products

1342899-48-2 ethyl 3-phenyl-2-n-propyl-1,2,5,10-tetrahydro-1,5,10-trioxobenzo[g]isoquinoline-4-carboxylate

19072-23-2Relevant academic research and scientific papers

Electrochemical Oxidative Cyclization: Synthesis of Polysubstituted Pyrrole from Enamines

Chen, Zhiwei,Shi, Guang,Tang, Wei,Sun, Jie,Wang, Wenxing

, p. 951 - 955 (2021/02/03)

A conceptually novel method for the preparation of pyrrole is described by electrochemical-oxidation-induced intermolecular annulation via enamines. In a simple undivided cell, based on a sodium acetate-facilitated, polysubstituted pyrrole derivations has been facilely synthesized under external oxidant-free condition. This electrosynthetic approach providing an environmentally benign protocol for C?C bond cross-coupling and oxidative annulation, which features unparalleled broad scope of substrates and practicality.

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