Cas 1022161-75-6,(2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis(1-methylpyrrolidine-2-carboxamide)

1022161-75-6

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Basic information

Product Name: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis(1-methylpyrrolidine-2-carboxamide)
Synonyms: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis(1-methylpyrrolidine-2-carboxamide)
CAS NO:1022161-75-6
Molecular Formula:
Molecular Weight: 434.582
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(1-methylpyrrolidine-2-carboxamide)(CAS DataBase Reference)
NIST Chemistry Reference: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis(1-methylpyrrolidine-2-carboxamide)(1022161-75-6)
EPA Substance Registry System: (2S,2'S)-N,N'-[(1S,2S)-1,2-diphenylethane-1,2-diyl] bis(1-methylpyrrolidine-2-carboxamide)(1022161-75-6)

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: 1022161-75-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1022161-75-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,2,1,6 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1022161-75:
(9*1)+(8*0)+(7*2)+(6*2)+(5*1)+(4*6)+(3*1)+(2*7)+(1*5)=86
86 % 10 = 6
So 1022161-75-6 is a valid CAS Registry Number.

1022161-75-6Upstream product

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1022161-75-6Relevant 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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