Cas 1262445-63-5,methyl 4-[(RS)-1-benzyl-4-(4-methoxybenzyl)-3,6-dioxopiperazin-2-yl]butanoate

1262445-63-5

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Basic information

Product Name: methyl 4-[(RS)-1-benzyl-4-(4-methoxybenzyl)-3,6-dioxopiperazin-2-yl]butanoate
Synonyms: methyl 4-[(RS)-1-benzyl-4-(4-methoxybenzyl)-3,6-dioxopiperazin-2-yl]butanoate
CAS NO:1262445-63-5
Molecular Formula:
Molecular Weight: 424.497
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 4-[(RS)-1-benzyl-4-(4-methoxybenzyl)-3,6-dioxopiperazin-2-yl]butanoate(CAS DataBase Reference)
NIST Chemistry Reference: methyl 4-[(RS)-1-benzyl-4-(4-methoxybenzyl)-3,6-dioxopiperazin-2-yl]butanoate(1262445-63-5)
EPA Substance Registry System: methyl 4-[(RS)-1-benzyl-4-(4-methoxybenzyl)-3,6-dioxopiperazin-2-yl]butanoate(1262445-63-5)

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: 1262445-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1262445-63-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,2,4,4 and 5 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1262445-63:
(9*1)+(8*2)+(7*6)+(6*2)+(5*4)+(4*4)+(3*5)+(2*6)+(1*3)=145
145 % 10 = 5
So 1262445-63-5 is a valid CAS Registry Number.

1262445-63-5Upstream product

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1262445-63-5Relevant academic research and scientific papers

Synthesis and biological evaluation of conformationally restricted σ1 receptor ligands with 7,9-diazabicyclo[4.2.2]decane scaffold

Sunnam, Sunil K.,Schepmann, Dirk,Rack, Elisabeth,Froehlich, Roland,Korpis, Katharina,Bednarski, Patrick J.,Wuensch, Bernhard

, p. 5525 - 5540 (2010)

The key step in the synthesis of the 7,9-diazabicyclo[4.2.2]decane system was a modified Dieckmann condensation of piperazinebutyrate 11, which makes use of trapping the first cyclized intermediate with TMS-Cl. Reduction of the bicyclic ketone 14 with LiB

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