Cas 212263-63-3,ethyl 5-(hex-5'-en-1'-yl)-2-phenyl-1-pyrroline-5-carboxylate 1-oxide

212263-63-3

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Basic information

Product Name: ethyl 5-(hex-5'-en-1'-yl)-2-phenyl-1-pyrroline-5-carboxylate 1-oxide
Synonyms: ethyl 5-(hex-5'-en-1'-yl)-2-phenyl-1-pyrroline-5-carboxylate 1-oxide
CAS NO:212263-63-3
Molecular Formula:
Molecular Weight: 315.412
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: ethyl 5-(hex-5'-en-1'-yl)-2-phenyl-1-pyrroline-5-carboxylate 1-oxide(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 5-(hex-5'-en-1'-yl)-2-phenyl-1-pyrroline-5-carboxylate 1-oxide(212263-63-3)
EPA Substance Registry System: ethyl 5-(hex-5'-en-1'-yl)-2-phenyl-1-pyrroline-5-carboxylate 1-oxide(212263-63-3)

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: 212263-63-3(Hazardous Substances Data)

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212263-63-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 212263-63-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,2,2,6 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 212263-63:
(8*2)+(7*1)+(6*2)+(5*2)+(4*6)+(3*3)+(2*6)+(1*3)=93
93 % 10 = 3
So 212263-63-3 is a valid CAS Registry Number.

212263-63-3Upstream product

212265-33-3 ethyl 2-phenyl-1-pyrroline-5-carboxylate 1-oxide

212263-63-3Downstream Products

212263-63-3Relevant academic research and scientific papers

Synthesis and radical reactions of isomeric alkenyl oxaziridines

Black, David St.C.,Edwards, Gavin L.,Laaman, Scan M.

, p. 1981 - 1990 (2007/10/03)

Several alkenyl oxaziridines were prepared either by photoisomerisation of the precursor nitrones, or by peracid oxidation of the analogous pyrrolines. In each case the oxaziridines were produced as separable mixtures of diastereoisomers, and reasons for

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