Cas 1028091-07-7,1-methyl-5-[1-(2-pyrrolidin-1-yl-phenyl)-methy-(E)-ylidene]-imidazolidine-2,4-dione

1028091-07-7

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Basic information

Product Name: 1-methyl-5-[1-(2-pyrrolidin-1-yl-phenyl)-methy-(E)-ylidene]-imidazolidine-2,4-dione
Synonyms:
CAS NO:1028091-07-7
Molecular Formula:
Molecular Weight: 271.319
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: 1-methyl-5-[1-(2-pyrrolidin-1-yl-phenyl)-methy-(E)-ylidene]-imidazolidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 1-methyl-5-[1-(2-pyrrolidin-1-yl-phenyl)-methy-(E)-ylidene]-imidazolidine-2,4-dione(1028091-07-7)
EPA Substance Registry System: 1-methyl-5-[1-(2-pyrrolidin-1-yl-phenyl)-methy-(E)-ylidene]-imidazolidine-2,4-dione(1028091-07-7)

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: 1028091-07-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1028091-07-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,8,0,9 and 1 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1028091-07:
(9*1)+(8*0)+(7*2)+(6*8)+(5*0)+(4*9)+(3*1)+(2*0)+(1*7)=117
117 % 10 = 7
So 1028091-07-7 is a valid CAS Registry Number.

1028091-07-7Upstream product

1028091-07-7Downstream Products

1028091-07-7Relevant academic research and scientific papers

Scope and limitations of the T-reaction employing some functionalized C-H-acids and naturally occurring secondary amines

Rabong, Constantin,Hametner, Christian,Mereiter, Kurt,Kartsev, Victor G.,Jordis, Ulrich

, p. 799 - 838 (2008/09/21)

Scope and limitations of the T-reaction with emphasis on using chiral, natural products as starting materials to prepare novel chiral heterocycles is studied and the diastereoselective introduction of newly formed stereocenters is explained via proposed mechanisms.

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