Cas 870283-26-4,4-Imidazolidinone, 2-(1,1-dimethylethyl)-3-methyl-5-[[1-(phenylmethyl)-1H-indol-3-yl]methyl] -, (2S,5S)-

870283-26-4

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Basic information

Product Name: 4-Imidazolidinone, 2-(1,1-dimethylethyl)-3-methyl-5-[[1-(phenylmethyl)-1H-indol-3-yl]methyl] -, (2S,5S)-
Synonyms:
CAS NO:870283-26-4
Molecular Formula: C24H29N3O
Molecular Weight: 375.514
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: 4-Imidazolidinone, 2-(1,1-dimethylethyl)-3-methyl-5-[[1-(phenylmethyl)-1H-indol-3-yl]methyl] -, (2S,5S)-(CAS DataBase Reference)
NIST Chemistry Reference: 4-Imidazolidinone, 2-(1,1-dimethylethyl)-3-methyl-5-[[1-(phenylmethyl)-1H-indol-3-yl]methyl] -, (2S,5S)-(870283-26-4)
EPA Substance Registry System: 4-Imidazolidinone, 2-(1,1-dimethylethyl)-3-methyl-5-[[1-(phenylmethyl)-1H-indol-3-yl]methyl] -, (2S,5S)-(870283-26-4)

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: 870283-26-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 870283-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,0,2,8 and 3 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 870283-26:
(8*8)+(7*7)+(6*0)+(5*2)+(4*8)+(3*3)+(2*2)+(1*6)=174
174 % 10 = 4
So 870283-26-4 is a valid CAS Registry Number.

870283-26-4Upstream product

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870283-26-4Relevant academic research and scientific papers

Preparation of the MacMillan imidazolidinones

Samulis, Leopold,Tomkinson, Nicholas C.O.

, p. 4263 - 4267 (2011)

A general method for the preparation of the MacMillan imidazolidinones is described. Treatment of an α-amino amide with a carbonyl compound in refluxing chloroform in the presence of Yb(OTf)3 (1 mol %) provides convenient access to the corresponding imidazolidinones.

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