Cas 421579-73-9,[(R)-3-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-prop-(E)-ylidene]-((S)-2-methoxymethyl-pyrrolidin-1-yl)-amine

421579-73-9

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Basic information

Product Name: [(R)-3-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-prop-(E)-ylidene]-((S)-2-methoxymethyl-pyrrolidin-1-yl)-amine
Synonyms:
CAS NO:421579-73-9
Molecular Formula:
Molecular Weight: 406.641
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: [(R)-3-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-prop-(E)-ylidene]-((S)-2-methoxymethyl-pyrrolidin-1-yl)-amine(CAS DataBase Reference)
NIST Chemistry Reference: [(R)-3-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-prop-(E)-ylidene]-((S)-2-methoxymethyl-pyrrolidin-1-yl)-amine(421579-73-9)
EPA Substance Registry System: [(R)-3-Benzyloxy-2-(tert-butyl-dimethyl-silanyloxy)-prop-(E)-ylidene]-((S)-2-methoxymethyl-pyrrolidin-1-yl)-amine(421579-73-9)

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: 421579-73-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 421579-73-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,2,1,5,7 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 421579-73:
(8*4)+(7*2)+(6*1)+(5*5)+(4*7)+(3*9)+(2*7)+(1*3)=149
149 % 10 = 9
So 421579-73-9 is a valid CAS Registry Number.

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421579-73-9Downstream Products

421579-73-9Relevant academic research and scientific papers

A short diastereo- and enantioselective synthesis of cis-4,5-disubstituted oxazolidin-2-ones

Enders,Kallfass,Nolte

, p. 33 - 36 (2007/10/03)

The asymmetric synthesis of cis-4,5-disubstituted oxazolidin-2-ones is described. Following a four step reaction sequence of α-alkylation, 1,2-addition with subsequent carbamate protection, cyclization and concluding with cleavage of the auxiliary the title compounds are obtained in moderate yields and in excellent diastereo- and enantiomeric excesses (de = 88 - > 96%, ee > 96%).

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