Cas 161126-76-7,6-Diethoxymethyl-4-dimethylamino-4-methyl-2-phenyl-4H-[1,3]selenazine-5-carbaldehyde

161126-76-7

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Basic information

Product Name: 6-Diethoxymethyl-4-dimethylamino-4-methyl-2-phenyl-4H-[1,3]selenazine-5-carbaldehyde
Synonyms: 6-Diethoxymethyl-4-dimethylamino-4-methyl-2-phenyl-4H-[1,3]selenazine-5-carbaldehyde
CAS NO:161126-76-7
Molecular Formula:
Molecular Weight: 409.387
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: 6-Diethoxymethyl-4-dimethylamino-4-methyl-2-phenyl-4H-[1,3]selenazine-5-carbaldehyde(CAS DataBase Reference)
NIST Chemistry Reference: 6-Diethoxymethyl-4-dimethylamino-4-methyl-2-phenyl-4H-[1,3]selenazine-5-carbaldehyde(161126-76-7)
EPA Substance Registry System: 6-Diethoxymethyl-4-dimethylamino-4-methyl-2-phenyl-4H-[1,3]selenazine-5-carbaldehyde(161126-76-7)

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: 161126-76-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161126-76-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,1,2 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 161126-76:
(8*1)+(7*6)+(6*1)+(5*1)+(4*2)+(3*6)+(2*7)+(1*6)=107
107 % 10 = 7
So 161126-76-7 is a valid CAS Registry Number.

161126-76-7Upstream product

161126-76-7Downstream Products

161126-76-7Relevant academic research and scientific papers

Easy access to substituted selenazine and selenopyran derivatives by a cycloaddition-cyclorersion process

Dubreuil, Didier,Pradere, Jean Paul,Giraudeau, Nathalie,Goli, Martin,Tonnard, Francois

, p. 237 - 240 (2007/10/02)

N′-selenoacylamidines were isolated by condensation of selenobenzamide with orthoamides. [4+2] cycloadditions with electrophilic dienophiles were performed leading to 1,3- selenazine derivatives. Selenoamide vinylogs obtained by thermolysis of 4H-1,3-sele

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