Cas 905855-85-8,2,2'-{[(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methyleneoxy)}bis(N,N-dibenzylethanamine)

905855-85-8

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Basic information

Product Name: 2,2'-{[(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methyleneoxy)}bis(N,N-dibenzylethanamine)
Synonyms: 2,2'-{[(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methyleneoxy)}bis(N,N-dibenzylethanamine)
CAS NO:905855-85-8
Molecular Formula:
Molecular Weight: 608.821
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: 2,2'-{[(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methyleneoxy)}bis(N,N-dibenzylethanamine)(CAS DataBase Reference)
NIST Chemistry Reference: 2,2'-{[(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methyleneoxy)}bis(N,N-dibenzylethanamine)(905855-85-8)
EPA Substance Registry System: 2,2'-{[(4S,5S)-2,2-dimethyl-1,3-dioxolane-4,5-diyl]bis(methyleneoxy)}bis(N,N-dibenzylethanamine)(905855-85-8)

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: 905855-85-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 905855-85-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,5,8,5 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 905855-85:
(8*9)+(7*0)+(6*5)+(5*8)+(4*5)+(3*5)+(2*8)+(1*5)=198
198 % 10 = 8
So 905855-85-8 is a valid CAS Registry Number.

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905855-85-8Relevant academic research and scientific papers

Anchimeric assistance in the case of vicinal dimesylate: Formation of enantiomeric or meso-bimorpholine

Kanger, Tonis,Laars, Marju,Kriis, Kadri,Kailas, Tiiu,Mueuerisepp, Aleksander-Mati,Pehk, Tonis,Lopp, Margus

, p. 1853 - 1857 (2006)

An anchimeric effect of vicinal dimesylate in the intramolecular nucleophilic substitution by amine is described. One sulfonate group of the dimesylate acts as an internal nucleophile and the other as a leaving group, affording meso-bimorpholine in the in

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