Cas 894419-50-2,N-{2-[4,5-dimethoxy-2-(2-oxo-2-phenylethyl)phenyl]-1-methylethyl}formamide

894419-50-2

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Basic information

Product Name: N-{2-[4,5-dimethoxy-2-(2-oxo-2-phenylethyl)phenyl]-1-methylethyl}formamide
Synonyms: N-{2-[4,5-dimethoxy-2-(2-oxo-2-phenylethyl)phenyl]-1-methylethyl}formamide
CAS NO:894419-50-2
Molecular Formula:
Molecular Weight: 341.407
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-{2-[4,5-dimethoxy-2-(2-oxo-2-phenylethyl)phenyl]-1-methylethyl}formamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{2-[4,5-dimethoxy-2-(2-oxo-2-phenylethyl)phenyl]-1-methylethyl}formamide(894419-50-2)
EPA Substance Registry System: N-{2-[4,5-dimethoxy-2-(2-oxo-2-phenylethyl)phenyl]-1-methylethyl}formamide(894419-50-2)

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: 894419-50-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 894419-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,4,4,1 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 894419-50:
(8*8)+(7*9)+(6*4)+(5*4)+(4*1)+(3*9)+(2*5)+(1*0)=212
212 % 10 = 2
So 894419-50-2 is a valid CAS Registry Number.

894419-50-2Upstream product

894419-50-2Downstream Products

52999-84-5 1-benzyl-6,7-dimethoxy-3-methyl-3,4-dihydro-isoquinoline

894419-50-2Relevant academic research and scientific papers

A synthesis of n-formylenamides of isoquinoline

Ivanov, Iliyan,Nikolova, Stoyanka,Statkova-Abeghe, Stela,Angelov, Plamen

, p. 387 - 393 (2007/10/03)

N-Formylenamides of isoquinoline (6) were obtained from N-[2-(2-acyl-4,5-dimethoxyphenyl)ethyl]formamides (5) by cyclization in the presence of catalytic amount of p-toluensulfonic acid. The starting keto formamides (5) were obtained by acylation of a N-[

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