Cas 122409-59-0,(1S)-N-<1-(benzyloxycarbonyl)-3-oxo-3-phenyl-propyl>-N<sup>ε</sup>-(tert-butoxycarbonyl)-(S)-lysyl-(S)-proline tert-butyl ester

122409-59-0

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Basic information

Product Name: (1S)-N-<1-(benzyloxycarbonyl)-3-oxo-3-phenyl-propyl>-N^ε-(tert-butoxycarbonyl)-(S)-lysyl-(S)-proline tert-butyl ester
Synonyms: (1S)-N-<1-(benzyloxycarbonyl)-3-oxo-3-phenyl-propyl>-N^ε-(tert-butoxycarbonyl)-(S)-lysyl-(S)-proline tert-butyl ester
CAS NO:122409-59-0
Molecular Formula:
Molecular Weight: 665.827
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: (1S)-N-<1-(benzyloxycarbonyl)-3-oxo-3-phenyl-propyl>-N^ε-(tert-butoxycarbonyl)-(S)-lysyl-(S)-proline tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (1S)-N-<1-(benzyloxycarbonyl)-3-oxo-3-phenyl-propyl>-N^ε-(tert-butoxycarbonyl)-(S)-lysyl-(S)-proline tert-butyl ester(122409-59-0)
EPA Substance Registry System: (1S)-N-<1-(benzyloxycarbonyl)-3-oxo-3-phenyl-propyl>-N^ε-(tert-butoxycarbonyl)-(S)-lysyl-(S)-proline tert-butyl ester(122409-59-0)

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: 122409-59-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 122409-59-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,4,0 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122409-59:
(8*1)+(7*2)+(6*2)+(5*4)+(4*0)+(3*9)+(2*5)+(1*9)=100
100 % 10 = 0
So 122409-59-0 is a valid CAS Registry Number.

122409-59-0Upstream product

122409-59-0Downstream Products

122409-59-0Relevant academic research and scientific papers

Studies Relating to the Configuration and Conformation of 3,5-Disubstituted Dihydro-2(3H)-furanones

Fischer, Janos,Fodor, Tamas,Dobay, Laszlo,Kiss, Bela,Toth, Gabor,et al.

, p. 1093 - 1098 (2007/10/02)

Internal prodrug analogues of enalapril were obtained by reduction of (1S)-N--(S)-alanyl-(S)-proline tert-butyl ester (1) to the alcohols 2a and 2b followed by lactonization to (3S,5S)- and (3S,5R)-N-(tetrahydro-2-

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