Cas 1105044-57-2,(2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis{2-[benzyl(methyl)amino]propanamide}

1105044-57-2

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Basic information

Product Name: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis{2-[benzyl(methyl)amino]propanamide}
Synonyms: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis{2-[benzyl(methyl)amino]propanamide}
CAS NO:1105044-57-2
Molecular Formula:
Molecular Weight: 562.755
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: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis{2-[benzyl(methyl)amino]propanamide}(CAS DataBase Reference)
NIST Chemistry Reference: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis{2-[benzyl(methyl)amino]propanamide}(1105044-57-2)
EPA Substance Registry System: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis{2-[benzyl(methyl)amino]propanamide}(1105044-57-2)

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: 1105044-57-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1105044-57-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,0,5,0,4 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1105044-57:
(9*1)+(8*1)+(7*0)+(6*5)+(5*0)+(4*4)+(3*4)+(2*5)+(1*7)=92
92 % 10 = 2
So 1105044-57-2 is a valid CAS Registry Number.

1105044-57-2Upstream product

1105044-57-2Downstream Products

1105044-57-2Relevant academic research and scientific papers

Synthesis of Yb complexes with amino-acid-armed ligands for direct asymmetric tandem aldol reduction reactions

Stodulski, Maciej,Jazwinski, Jaroslaw,Mlynarski, Jacek

experimental part, p. 5553 - 5562 (2009/05/11)

A synthetic route to a series of C2-symmetric chiral ligands armed with selectively protected amino acids have been developed with the aim to study the potential of the corresponding Yb(III) complexes for enantioselective direct aldol reactions

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