Cas 1420293-04-4,N-benzylidene-1-(2-(3,3-dimethoxypropyl)-4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)-2-methoxy-2-oxoethanamine oxide

1420293-04-4

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Basic information

Product Name: N-benzylidene-1-(2-(3,3-dimethoxypropyl)-4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)-2-methoxy-2-oxoethanamine oxide
Synonyms: N-benzylidene-1-(2-(3,3-dimethoxypropyl)-4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)-2-methoxy-2-oxoethanamine oxide
CAS NO:1420293-04-4
Molecular Formula:
Molecular Weight: 423.507
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-benzylidene-1-(2-(3,3-dimethoxypropyl)-4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)-2-methoxy-2-oxoethanamine oxide(CAS DataBase Reference)
NIST Chemistry Reference: N-benzylidene-1-(2-(3,3-dimethoxypropyl)-4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)-2-methoxy-2-oxoethanamine oxide(1420293-04-4)
EPA Substance Registry System: N-benzylidene-1-(2-(3,3-dimethoxypropyl)-4,4,5,5-tetramethyl-1,3-dioxolan-2-yl)-2-methoxy-2-oxoethanamine oxide(1420293-04-4)

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: 1420293-04-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1420293-04-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,0,2,9 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1420293-04:
(9*1)+(8*4)+(7*2)+(6*0)+(5*2)+(4*9)+(3*3)+(2*0)+(1*4)=114
114 % 10 = 4
So 1420293-04-4 is a valid CAS Registry Number.

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1420293-04-4Relevant academic research and scientific papers

Functional-group-tolerant catalytic migratory oxidative coupling of nitrones

Hashizume, Shogo,Oisaki, Kounosuke,Kanai, Motomu

, p. 2600 - 2606,7 (2012)

A copper-catalyzed migratory oxidative-coupling reaction between nitrones and various ethers/amines exhibited high functional-group tolerance. Even in aqueous media, the reaction proceeded efficiently. For practical use of this catalysis, a unique sequent

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