Cas 885603-54-3,N,N-[(S)-1-(naphthalen-2-yl)ethyl][(S)-1-(2-methoxyphenyl)ethyl]-amine

885603-54-3

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Basic information

Product Name: N,N-[(S)-1-(naphthalen-2-yl)ethyl][(S)-1-(2-methoxyphenyl)ethyl]-amine
Synonyms: N,N-[(S)-1-(naphthalen-2-yl)ethyl][(S)-1-(2-methoxyphenyl)ethyl]-amine
CAS NO:885603-54-3
Molecular Formula:
Molecular Weight: 305.42
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: N,N-[(S)-1-(naphthalen-2-yl)ethyl][(S)-1-(2-methoxyphenyl)ethyl]-amine(CAS DataBase Reference)
NIST Chemistry Reference: N,N-[(S)-1-(naphthalen-2-yl)ethyl][(S)-1-(2-methoxyphenyl)ethyl]-amine(885603-54-3)
EPA Substance Registry System: N,N-[(S)-1-(naphthalen-2-yl)ethyl][(S)-1-(2-methoxyphenyl)ethyl]-amine(885603-54-3)

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: 885603-54-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 885603-54-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,5,6,0 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 885603-54:
(8*8)+(7*8)+(6*5)+(5*6)+(4*0)+(3*3)+(2*5)+(1*4)=203
203 % 10 = 3
So 885603-54-3 is a valid CAS Registry Number.

885603-54-3Upstream product

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885603-54-3Relevant academic research and scientific papers

Catalytic asymmetric transformations with fine-tunable biphenol-based monodentate ligands

Chapsal, Bruno D.,Hua, Zihao,Ojima, Iwao

, p. 642 - 657 (2006)

A library of new fine-tunable monodentate phosphite and phosphoramidite ligands based on chiral biphenol have been designed and developed. These monodentate phosphorus ligands have exhibited excellent enantioselectivity in the Pd-catalyzed asymmetric allylic alkylation and Rh-catalyzed asymmetric hydrogenation.

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