Cas 174222-04-9,(2R,3S)-3-(tert-Butyl-diphenyl-silanyloxy)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester

174222-04-9

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Basic information

Product Name: (2R,3S)-3-(tert-Butyl-diphenyl-silanyloxy)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester
Synonyms:
CAS NO:174222-04-9
Molecular Formula:
Molecular Weight: 453.654
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: (2R,3S)-3-(tert-Butyl-diphenyl-silanyloxy)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3S)-3-(tert-Butyl-diphenyl-silanyloxy)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester(174222-04-9)
EPA Substance Registry System: (2R,3S)-3-(tert-Butyl-diphenyl-silanyloxy)-2-formyl-pyrrolidine-1-carboxylic acid tert-butyl ester(174222-04-9)

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: 174222-04-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 174222-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,4,2,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 174222-04:
(8*1)+(7*7)+(6*4)+(5*2)+(4*2)+(3*2)+(2*0)+(1*4)=109
109 % 10 = 9
So 174222-04-9 is a valid CAS Registry Number.

174222-04-9Upstream product

174222-03-8 (2S,3S)-N-(tert-butoxycarbonyl)-3-(tert-butyldiphenylsiloxy)-2-(hydroxymethyl)pyrrolidine

174222-04-9Downstream Products

174222-05-0 (3R)-tert-butyl 3-hydroxy-3-((2S,3S)-3-(tert-butyldiphenylsiloxy)-N-(tert-butoxycarbonyl)-2-pyrrolidinyl)propionate

174222-04-9Relevant academic research and scientific papers

Total synthesis of cis- and trans-3-hydroxy-D-proline and (+)-detoxinine

Mulzer, Johann,Meier, Andreas,Buschmann, Juergen,Luger, Peter

, p. 566 - 572 (1996)

The unnatural enantiomer of the amino acid detoxinine and both diastereomeric 3-hydroxy-D-prolines have been prepared from D-mannitol via the O-silylated hydroxyproline 12 as a common key intermediate.

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