Cas 1159486-41-5,2-[2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-4-phenyl-butyl]-malonic acid dimethyl ester

1159486-41-5

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Basic information

Product Name: 2-[2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-4-phenyl-butyl]-malonic acid dimethyl ester
Synonyms: 2-[2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-4-phenyl-butyl]-malonic acid dimethyl ester
CAS NO:1159486-41-5
Molecular Formula:
Molecular Weight: 546.748
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: 2-[2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-4-phenyl-butyl]-malonic acid dimethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: 2-[2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-4-phenyl-butyl]-malonic acid dimethyl ester(1159486-41-5)
EPA Substance Registry System: 2-[2-(4-tert-butyl-2,2,6,6-tetraethyl-3-oxo-piperazin-1-yloxy)-4-phenyl-butyl]-malonic acid dimethyl ester(1159486-41-5)

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: 1159486-41-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1159486-41-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,9,4,8 and 6 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1159486-41:
(9*1)+(8*1)+(7*5)+(6*9)+(5*4)+(4*8)+(3*6)+(2*4)+(1*1)=185
185 % 10 = 5
So 1159486-41-5 is a valid CAS Registry Number.

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1159486-41-5Relevant academic research and scientific papers

Microflow radical carboaminoxylations with a novel alkoxyamine

Wienhoefer, Inga C.,Studer, Armido,Rahman, Taifur,Fukuyama, Takahide,Ryu, Ilhyong

, p. 2457 - 2460 (2009)

Highly efficient thermal radical carboaminoxylations of various olefins by using the novel alkoxyamine A to give adducts of type B are described. It is reported that these radical addition reactions can be performed in a microflow reaction system. As comp

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