Cas 1262797-10-3,(3R,5R,7R,7aS)-1-benzyl-5-t-butoxycarbonyl-7-cyano-7-methyl-3-phenylhexahydropyrrolo[1,2-a]imidazole

1262797-10-3

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Basic information

Product Name: (3R,5R,7R,7aS)-1-benzyl-5-t-butoxycarbonyl-7-cyano-7-methyl-3-phenylhexahydropyrrolo[1,2-a]imidazole
Synonyms:
CAS NO:1262797-10-3
Molecular Formula:
Molecular Weight: 417.551
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: (3R,5R,7R,7aS)-1-benzyl-5-t-butoxycarbonyl-7-cyano-7-methyl-3-phenylhexahydropyrrolo[1,2-a]imidazole(CAS DataBase Reference)
NIST Chemistry Reference: (3R,5R,7R,7aS)-1-benzyl-5-t-butoxycarbonyl-7-cyano-7-methyl-3-phenylhexahydropyrrolo[1,2-a]imidazole(1262797-10-3)
EPA Substance Registry System: (3R,5R,7R,7aS)-1-benzyl-5-t-butoxycarbonyl-7-cyano-7-methyl-3-phenylhexahydropyrrolo[1,2-a]imidazole(1262797-10-3)

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: 1262797-10-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262797-10-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,7,9 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1262797-10:
(9*1)+(8*2)+(7*6)+(6*2)+(5*7)+(4*9)+(3*7)+(2*1)+(1*0)=173
173 % 10 = 3
So 1262797-10-3 is a valid CAS Registry Number.

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1262797-10-3Relevant academic research and scientific papers

Cycloaddition of homochiral dihydroimidazoles: A 1,3-dipolar cycloaddition route to optically active pyrrolo[1,2-a]imidazoles

Jones, Raymond C. F.,Howard, Kevin J.,Snaith, John S.,Blake, Alexander J.,Li, Wang-Shei,Steel, Peter J.

experimental part, p. 297 - 306 (2011/02/23)

N-Alkylation of optically active 1-benzyl-4-phenyl-4,5-dihydroimidazole with active alkyl halides and treatment of the so-formed 4,5-dihydroimidazolium ions with DBU in the presence of a range of electron-deficient alkene dipolarophiles, constitutes a 'on

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