Cas 1131377-07-5,2-(4-chlorophenyl)-4-di(4-methylphenyl)methylene-3-diphenylmethylene-1-phenylpyrrolidine

1131377-07-5

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Basic information

Product Name: 2-(4-chlorophenyl)-4-di(4-methylphenyl)methylene-3-diphenylmethylene-1-phenylpyrrolidine
Synonyms:
CAS NO:1131377-07-5
Molecular Formula:
Molecular Weight: 614.23
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-(4-chlorophenyl)-4-di(4-methylphenyl)methylene-3-diphenylmethylene-1-phenylpyrrolidine(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-chlorophenyl)-4-di(4-methylphenyl)methylene-3-diphenylmethylene-1-phenylpyrrolidine(1131377-07-5)
EPA Substance Registry System: 2-(4-chlorophenyl)-4-di(4-methylphenyl)methylene-3-diphenylmethylene-1-phenylpyrrolidine(1131377-07-5)

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: 1131377-07-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1131377-07-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,3,1,3,7 and 7 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1131377-07:
(9*1)+(8*1)+(7*3)+(6*1)+(5*3)+(4*7)+(3*7)+(2*0)+(1*7)=115
115 % 10 = 5
So 1131377-07-5 is a valid CAS Registry Number.

1131377-07-5Upstream product

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1131377-07-5Relevant academic research and scientific papers

Synthesis of substituted pyrrolidines by reaction of aryl-substituted vinylidenecyclopropanes with aromatic imines catalyzed by BF3· Et2O

Stepakov,Larina,Radina,Boitsov,Molchanov

experimental part, p. 430 - 434 (2009/04/04)

The reactions of 1,1-diaryl-2-(diphenylvinylidene)cyclopropanes and 1,1-diaryl-2-(2-phenylpropenylidine) cyclopropanes with aromatic amines in the presence of BF3·Et2O leads to the formation of pyrrolidine derivatives.

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