Cas 83466-93-7,dimethyl 5,6,7,7a-tetrahydro-1-(phenoxymethyl)-3-phenyl-1H-pyrrolizine-1,2-dicarboxylate

83466-93-7

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Basic information

Product Name: dimethyl 5,6,7,7a-tetrahydro-1-(phenoxymethyl)-3-phenyl-1H-pyrrolizine-1,2-dicarboxylate
Synonyms: dimethyl 5,6,7,7a-tetrahydro-1-(phenoxymethyl)-3-phenyl-1H-pyrrolizine-1,2-dicarboxylate
CAS NO:83466-93-7
Molecular Formula:
Molecular Weight: 407.466
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: dimethyl 5,6,7,7a-tetrahydro-1-(phenoxymethyl)-3-phenyl-1H-pyrrolizine-1,2-dicarboxylate(CAS DataBase Reference)
NIST Chemistry Reference: dimethyl 5,6,7,7a-tetrahydro-1-(phenoxymethyl)-3-phenyl-1H-pyrrolizine-1,2-dicarboxylate(83466-93-7)
EPA Substance Registry System: dimethyl 5,6,7,7a-tetrahydro-1-(phenoxymethyl)-3-phenyl-1H-pyrrolizine-1,2-dicarboxylate(83466-93-7)

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: 83466-93-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83466-93-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,4,6 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83466-93:
(7*8)+(6*3)+(5*4)+(4*6)+(3*6)+(2*9)+(1*3)=157
157 % 10 = 7
So 83466-93-7 is a valid CAS Registry Number.

83466-93-7Upstream product

67395-14-6 2-[1-Phenoxy-meth-(E)-ylidene]-3-[1-phenyl-1-pyrrolidin-1-yl-meth-(E)-ylidene]-succinic acid dimethyl ester

83466-93-7Downstream Products

83466-93-7Relevant academic research and scientific papers

1-Pyrrolidin-1-ylbuta-1,3-dienes as Potential 1,5-Dipoles; Synthesis of Pyrrolizines

Visser, Germ W.,Verboom, Willem,Benders, Piet H.,Reinhoudt, David N.

, p. 669 - 671 (1982)

Tautomerization of 1-pyrrolidin-1-ylbuta-1,3-dienes and (hetero)aromatic compounds formally containing this moiety, to the corresponding 1,5-dipoles by a concerted hydrogen shift is followed by a 1,5-electrocyclization to give pyrrolizine derivative

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