Cas 26163-79-1,(E)-1-morpholino-3-(p-tolyl)prop-2-en-1-one

26163-79-1

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Basic information

Product Name: (E)-1-morpholino-3-(p-tolyl)prop-2-en-1-one
Synonyms: (E)-1-morpholino-3-(p-tolyl)prop-2-en-1-one
CAS NO:26163-79-1
Molecular Formula:
Molecular Weight: 231.294
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: (E)-1-morpholino-3-(p-tolyl)prop-2-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-morpholino-3-(p-tolyl)prop-2-en-1-one(26163-79-1)
EPA Substance Registry System: (E)-1-morpholino-3-(p-tolyl)prop-2-en-1-one(26163-79-1)

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: 26163-79-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 26163-79-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,6 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 26163-79:
(7*2)+(6*6)+(5*1)+(4*6)+(3*3)+(2*7)+(1*9)=111
111 % 10 = 1
So 26163-79-1 is a valid CAS Registry Number.

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26163-79-1Downstream Products

26163-79-1Relevant academic research and scientific papers

(E)-α,β-unsaturated amides from tertiary amines, olefins and CO via Pd/Cu-catalyzed aerobic oxidative N-dealkylation

Shi, Renyi,Zhang, Hua,Lu, Lijun,Gan, Pei,Sha, Yuchen,Zhang, Heng,Liu, Qiang,Beller, Matthias,Lei, Aiwen

, p. 3247 - 3250 (2015)

A novel Pd/Cu-catalyzed chemoselective aerobic oxidative N-dealkylation/carbonylation reaction has been developed. Tertiary amines are utilized as a "reservoir" of "active" secondary amines in this transformation, which inhibits the formation of undesired by-products and the deactivation of the catalysts. This protocol allows for an efficient and straightforward construction of synthetically useful and bioactive (E)-α,β-unsaturated amide derivatives from easily available tertiary amines, olefins and CO. This journal is

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