Cas 214400-48-3,(R)-2-[(R)-((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester

214400-48-3

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Basic information

Product Name: (R)-2-[(R)-((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
Synonyms: (R)-2-[(R)-((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester
CAS NO:214400-48-3
Molecular Formula:
Molecular Weight: 421.534
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)-2-[(R)-((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-[(R)-((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(214400-48-3)
EPA Substance Registry System: (R)-2-[(R)-((4R,5R)-5-Benzyloxymethyl-2,2-dimethyl-[1,3]dioxolan-4-yl)-hydroxy-methyl]-pyrrolidine-1-carboxylic acid tert-butyl ester(214400-48-3)

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: 214400-48-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 214400-48-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,4,4,0 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 214400-48:
(8*2)+(7*1)+(6*4)+(5*4)+(4*0)+(3*0)+(2*4)+(1*8)=83
83 % 10 = 3
So 214400-48-3 is a valid CAS Registry Number.

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214400-48-3Relevant academic research and scientific papers

Stereoselective synthesis of hydroxyindolizidines via sparteine-assisted deprotonation of N-Boc-pyrrolidine

Majewski, Marek,Shao, Jianxing,Nelson, Ken,Nowak, Pawel,Irvine, Nicholas M.

, p. 6787 - 6790 (2007/10/03)

Three diastereoisomers of 1-deoxycastanospermine were synthesized in enantiomerically pure form. The key step in the synthesis involved reaction of lithiated N-Boc-pyrrolidine in the presence of sparteine with a chiral building block derived from tartaric acid.

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