Cas 849752-69-8,[(S)-1-[(S)-1-(2-hydroxy-4-methoxybenzylcarbamoyl)-2-methylpropylcarbamoyl]-2-(3,4,5-trimethoxyphenyl)ethyl]carbamic acid tert-butyl ester

849752-69-8

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Basic information

Product Name: [(S)-1-[(S)-1-(2-hydroxy-4-methoxybenzylcarbamoyl)-2-methylpropylcarbamoyl]-2-(3,4,5-trimethoxyphenyl)ethyl]carbamic acid tert-butyl ester
Synonyms: [(S)-1-[(S)-1-(2-hydroxy-4-methoxybenzylcarbamoyl)-2-methylpropylcarbamoyl]-2-(3,4,5-trimethoxyphenyl)ethyl]carbamic acid tert-butyl ester
CAS NO:849752-69-8
Molecular Formula:
Molecular Weight: 589.686
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: [(S)-1-[(S)-1-(2-hydroxy-4-methoxybenzylcarbamoyl)-2-methylpropylcarbamoyl]-2-(3,4,5-trimethoxyphenyl)ethyl]carbamic acid tert-butyl ester(CAS DataBase Reference)
NIST Chemistry Reference: [(S)-1-[(S)-1-(2-hydroxy-4-methoxybenzylcarbamoyl)-2-methylpropylcarbamoyl]-2-(3,4,5-trimethoxyphenyl)ethyl]carbamic acid tert-butyl ester(849752-69-8)
EPA Substance Registry System: [(S)-1-[(S)-1-(2-hydroxy-4-methoxybenzylcarbamoyl)-2-methylpropylcarbamoyl]-2-(3,4,5-trimethoxyphenyl)ethyl]carbamic acid tert-butyl ester(849752-69-8)

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: 849752-69-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 849752-69-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,9,7,5 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 849752-69:
(8*8)+(7*4)+(6*9)+(5*7)+(4*5)+(3*2)+(2*6)+(1*9)=228
228 % 10 = 8
So 849752-69-8 is a valid CAS Registry Number.

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849752-69-8Relevant academic research and scientific papers

Entry into a new class of potent proteasome inhibitors having high antiproliferative activity by structure-based design

Furet, Pascal,Imbach, Patricia,Noorani, Maria,Koeppler, Juergen,Laumen, Kurt,Lang, Marc,Guagnano, Vito,Fuerst, Peter,Roesel, Johannes,Zimmermann, Johann,García-Echeverría, Carlos

, p. 4810 - 4813 (2004)

Proteasome inhibition is a therapeutic concept of current interest in anticancer research. We report here the design, synthesis, and biological characterization of prototypes of a new class of noncovalent proteasome inhibitors showing high activity in bio

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