Cas 913059-68-4,(2R,3R,5S)-3-((R)-1-Hydroxy-but-3-enyl)-5-phenyl-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid

913059-68-4

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Basic information

Product Name: (2R,3R,5S)-3-((R)-1-Hydroxy-but-3-enyl)-5-phenyl-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid
Synonyms: (2R,3R,5S)-3-((R)-1-Hydroxy-but-3-enyl)-5-phenyl-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid
CAS NO:913059-68-4
Molecular Formula:
Molecular Weight: 415.51
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,3R,5S)-3-((R)-1-Hydroxy-but-3-enyl)-5-phenyl-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,5S)-3-((R)-1-Hydroxy-but-3-enyl)-5-phenyl-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid(913059-68-4)
EPA Substance Registry System: (2R,3R,5S)-3-((R)-1-Hydroxy-but-3-enyl)-5-phenyl-1-(toluene-4-sulfonyl)-pyrrolidine-2-carboxylic acid(913059-68-4)

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: 913059-68-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 913059-68-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,3,0,5 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 913059-68:
(8*9)+(7*1)+(6*3)+(5*0)+(4*5)+(3*9)+(2*6)+(1*8)=164
164 % 10 = 4
So 913059-68-4 is a valid CAS Registry Number.

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913059-68-4Relevant academic research and scientific papers

Asymmetric multicomponent reactions: Diastereoselective synthesis of substituted pyrrolidines and prolines

Ghosh, Arun K.,Kulkarni, Sarang,Xu, Chun-Xiao,Fanwick, Phillip E.

, p. 4509 - 4511 (2006)

A novel diastereoselective synthesis of substituted pyrrolidines has been developed. Asymmetric multicomponent reactions of optically active phenyldihydrofuran, N-tosyl imino ester, and silane reagents in a one-pot operation afforded highly substituted py

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