Cas 231609-72-6,N,3-dimethyl-N-methoxy-2-(1-methyl-3-oxo-3-phenyl-1-propenylamino)butyramide

231609-72-6

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Basic information

Product Name: N,3-dimethyl-N-methoxy-2-(1-methyl-3-oxo-3-phenyl-1-propenylamino)butyramide
Synonyms: N,3-dimethyl-N-methoxy-2-(1-methyl-3-oxo-3-phenyl-1-propenylamino)butyramide
CAS NO:231609-72-6
Molecular Formula:
Molecular Weight: 304.389
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,3-dimethyl-N-methoxy-2-(1-methyl-3-oxo-3-phenyl-1-propenylamino)butyramide(CAS DataBase Reference)
NIST Chemistry Reference: N,3-dimethyl-N-methoxy-2-(1-methyl-3-oxo-3-phenyl-1-propenylamino)butyramide(231609-72-6)
EPA Substance Registry System: N,3-dimethyl-N-methoxy-2-(1-methyl-3-oxo-3-phenyl-1-propenylamino)butyramide(231609-72-6)

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: 231609-72-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 231609-72-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,1,6,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 231609-72:
(8*2)+(7*3)+(6*1)+(5*6)+(4*0)+(3*9)+(2*7)+(1*2)=116
116 % 10 = 6
So 231609-72-6 is a valid CAS Registry Number.

231609-72-6Upstream product

23652-90-6 3-amino-1-phenylbut-2-en-1-one

231609-72-6Downstream Products

231609-72-6Relevant academic research and scientific papers

Versatility of Weinreb amides in the Knorr pyrrole synthesis

Alberola, Angel,Ortega, Alfonso Gonzalez,Sadaba, M. Luisa,Sanudo, Carmen

, p. 6555 - 6566 (1999)

N-Methoxy-N-methyl-α-enaminocarboxamides were prepared starting from enamines and Weinreb α-aminoamides. Their reaction with oganometallic compounds and subsequent cyclization constitute a versatile alternative in the Knorr pyrrole synthesis.

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