Cas 1026076-65-2,{(R)-1-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-3-phenyl-propyl]-pentyl}-((S)-2-methoxymethyl-pyrrolidin-1-yl)-carbamic acid methyl ester

1026076-65-2

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Basic information

Product Name: {(R)-1-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-3-phenyl-propyl]-pentyl}-((S)-2-methoxymethyl-pyrrolidin-1-yl)-carbamic acid methyl ester
Synonyms:
CAS NO:1026076-65-2
Molecular Formula:
Molecular Weight: 506.801
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)-1-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-3-phenyl-propyl]-pentyl}-((S)-2-methoxymethyl-pyrrolidin-1-yl)-carbamic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: {(R)-1-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-3-phenyl-propyl]-pentyl}-((S)-2-methoxymethyl-pyrrolidin-1-yl)-carbamic acid methyl ester(1026076-65-2)
EPA Substance Registry System: {(R)-1-[(S)-1-(tert-Butyl-dimethyl-silanyloxy)-3-phenyl-propyl]-pentyl}-((S)-2-methoxymethyl-pyrrolidin-1-yl)-carbamic acid methyl ester(1026076-65-2)

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: 1026076-65-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1026076-65-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,2,6,0,7 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1026076-65:
(9*1)+(8*0)+(7*2)+(6*6)+(5*0)+(4*7)+(3*6)+(2*6)+(1*5)=122
122 % 10 = 2
So 1026076-65-2 is a valid CAS Registry Number.

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1026076-65-2Relevant 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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