Cas 1060662-60-3,methyl (2R)-3-benzyloxy-2-[4'-(tert-butoxycarbonyl)-2'-oxopiperazin-1'-yl]propanoate

1060662-60-3

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Basic information

Product Name: methyl (2R)-3-benzyloxy-2-[4'-(tert-butoxycarbonyl)-2'-oxopiperazin-1'-yl]propanoate
Synonyms: methyl (2R)-3-benzyloxy-2-[4'-(tert-butoxycarbonyl)-2'-oxopiperazin-1'-yl]propanoate
CAS NO:1060662-60-3
Molecular Formula:
Molecular Weight: 392.452
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: methyl (2R)-3-benzyloxy-2-[4'-(tert-butoxycarbonyl)-2'-oxopiperazin-1'-yl]propanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl (2R)-3-benzyloxy-2-[4'-(tert-butoxycarbonyl)-2'-oxopiperazin-1'-yl]propanoate(1060662-60-3)
EPA Substance Registry System: methyl (2R)-3-benzyloxy-2-[4'-(tert-butoxycarbonyl)-2'-oxopiperazin-1'-yl]propanoate(1060662-60-3)

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: 1060662-60-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1060662-60-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,0,6,6 and 2 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1060662-60:
(9*1)+(8*0)+(7*6)+(6*0)+(5*6)+(4*6)+(3*2)+(2*6)+(1*0)=123
123 % 10 = 3
So 1060662-60-3 is a valid CAS Registry Number.

1060662-60-3Upstream product

1060662-54-5 methyl (2R)-3-benzyloxy-2-[4'-(tert-butoxycarbonyl)-1'-piperazinyl]propanoate

1060662-60-3Downstream Products

1060662-60-3Relevant academic research and scientific papers

New efficient enantioselective synthesis of 2-oxopiperazines: a practical access to chiral 3-substituted 2-oxopiperazines

Lencina, Claiton Leoneti,Dassonville-Klimpt, Alexandra,Sonnet, Pascal

, p. 1689 - 1697 (2008/12/21)

The development of efficient and stereoselective methods to produce 1,4-disubstituted-2-oxopiperazine in enantiomerically pure form, from a readily available starting material is crucial. Herein, we report a reduction modification to our previously descri

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