Cas 853879-00-2,(4R,5S)-1,5-Dimethyl-3-((2S,5R)-5-naphthalen-1-yl-2,5-dihydro-furan-2-yl)-4-phenyl-imidazolidin-2-one

853879-00-2

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Basic information

Product Name: (4R,5S)-1,5-Dimethyl-3-((2S,5R)-5-naphthalen-1-yl-2,5-dihydro-furan-2-yl)-4-phenyl-imidazolidin-2-one
Synonyms: (4R,5S)-1,5-Dimethyl-3-((2S,5R)-5-naphthalen-1-yl-2,5-dihydro-furan-2-yl)-4-phenyl-imidazolidin-2-one
CAS NO:853879-00-2
Molecular Formula:
Molecular Weight: 384.478
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: (4R,5S)-1,5-Dimethyl-3-((2S,5R)-5-naphthalen-1-yl-2,5-dihydro-furan-2-yl)-4-phenyl-imidazolidin-2-one(CAS DataBase Reference)
NIST Chemistry Reference: (4R,5S)-1,5-Dimethyl-3-((2S,5R)-5-naphthalen-1-yl-2,5-dihydro-furan-2-yl)-4-phenyl-imidazolidin-2-one(853879-00-2)
EPA Substance Registry System: (4R,5S)-1,5-Dimethyl-3-((2S,5R)-5-naphthalen-1-yl-2,5-dihydro-furan-2-yl)-4-phenyl-imidazolidin-2-one(853879-00-2)

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: 853879-00-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 853879-00-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,3,8,7 and 9 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 853879-00:
(8*8)+(7*5)+(6*3)+(5*8)+(4*7)+(3*9)+(2*0)+(1*0)=212
212 % 10 = 2
So 853879-00-2 is a valid CAS Registry Number.

853879-00-2Upstream product

853879-00-2Downstream Products

853879-00-2Relevant academic research and scientific papers

Syntheses of 2,5-disubstituted dihydrofurans from γ-substituted chiral allenamides

Berry, Craig R.,Hsung, Richard P.,Antoline, Jennifer E.,Petersen, Matthew E.,Challeppan, Rameshkumar,Nielson, Jessica A.

, p. 4038 - 4042 (2007/10/03)

Details of a synthesis of dihydrofurans using γ-substituted chiral allenamides are described here. Some transformations of these dihydrofurans are also examined including a highly stereoselective dihydroxylation and a rare account of a Lewis acid-mediated

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