Cas 248253-41-0,{2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-piperidin-1-yl}-(3,4-dimethoxy-phenyl)-methanone

248253-41-0

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Basic information

Product Name: {2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-piperidin-1-yl}-(3,4-dimethoxy-phenyl)-methanone
Synonyms: {2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-piperidin-1-yl}-(3,4-dimethoxy-phenyl)-methanone
CAS NO:248253-41-0
Molecular Formula:
Molecular Weight: 381.428
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: {2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-piperidin-1-yl}-(3,4-dimethoxy-phenyl)-methanone(CAS DataBase Reference)
NIST Chemistry Reference: {2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-piperidin-1-yl}-(3,4-dimethoxy-phenyl)-methanone(248253-41-0)
EPA Substance Registry System: {2-[1-Benzo[1,3]dioxol-5-yl-meth-(E)-ylidene]-piperidin-1-yl}-(3,4-dimethoxy-phenyl)-methanone(248253-41-0)

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: 248253-41-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 248253-41-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,8,2,5 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 248253-41:
(8*2)+(7*4)+(6*8)+(5*2)+(4*5)+(3*3)+(2*4)+(1*1)=140
140 % 10 = 0
So 248253-41-0 is a valid CAS Registry Number.

248253-41-0Upstream product

248253-41-0Downstream Products

248253-47-6 (2-benzo[1,3]dioxol-5-ylmethyl-piperidin-1-yl)-(3,4-dimethoxy-phenyl)-methanone

248253-41-0Relevant academic research and scientific papers

An efficient synthesis of 5-(or 6-)-arylbenzoindolizidine and - quinolizidine derivatives

Lebrun, Stephane,Couture, Axel,Deniau, Eric,Grandclaudon, Pierre

, p. 2345 - 2352 (2007/10/03)

A new methodology for the synthesis of (hetero)arylated benzomdolizidine and benzoquinolizidine derivatives through sequential reduction of pyrrolidine- and piperidine-based aromatic enamides, and ultimate cyclization, is reported.

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