Cas 928824-19-5,(S)-N-[(R)-1-(2,4-Dimethoxy-benzyl)-3-isobutyl-2-oxo-azetidin-3-yl]-3-methyl-2-{(S)-2-[2-(3-phenoxy-phenyl)-acetylamino]-3-phenyl-propionylamino}-butyramide

928824-19-5

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Basic information

Product Name: (S)-N-[(R)-1-(2,4-Dimethoxy-benzyl)-3-isobutyl-2-oxo-azetidin-3-yl]-3-methyl-2-{(S)-2-[2-(3-phenoxy-phenyl)-acetylamino]-3-phenyl-propionylamino}-butyramide
Synonyms:
CAS NO:928824-19-5
Molecular Formula:
Molecular Weight: 748.919
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)-N-[(R)-1-(2,4-Dimethoxy-benzyl)-3-isobutyl-2-oxo-azetidin-3-yl]-3-methyl-2-{(S)-2-[2-(3-phenoxy-phenyl)-acetylamino]-3-phenyl-propionylamino}-butyramide(CAS DataBase Reference)
NIST Chemistry Reference: (S)-N-[(R)-1-(2,4-Dimethoxy-benzyl)-3-isobutyl-2-oxo-azetidin-3-yl]-3-methyl-2-{(S)-2-[2-(3-phenoxy-phenyl)-acetylamino]-3-phenyl-propionylamino}-butyramide(928824-19-5)
EPA Substance Registry System: (S)-N-[(R)-1-(2,4-Dimethoxy-benzyl)-3-isobutyl-2-oxo-azetidin-3-yl]-3-methyl-2-{(S)-2-[2-(3-phenoxy-phenyl)-acetylamino]-3-phenyl-propionylamino}-butyramide(928824-19-5)

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: 928824-19-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 928824-19-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,8,8,2 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 928824-19:
(8*9)+(7*2)+(6*8)+(5*8)+(4*2)+(3*4)+(2*1)+(1*9)=205
205 % 10 = 5
So 928824-19-5 is a valid CAS Registry Number.

928824-19-5Upstream product

928824-19-5Downstream Products

928824-19-5Relevant academic research and scientific papers

Novel β-lactam derivatives: Potent and selective inhibitors of the chymotrypsin-like activity of the human 20S proteasome

Imbach, Patricia,Lang, Marc,Garcia-Echeverria, Carlos,Guagnano, Vito,Noorani, Maria,Roesel, Johannes,Bitsch, Francis,Rihs, Grety,Furet, Pascal

, p. 358 - 362 (2007/10/03)

A series of β-lactam derivatives has been designed and synthesized to inhibit the chymotrypsin-like activity of the human 20S proteasome. The most potent compounds of this new structural class of β-subunit selective 20S proteasome inhibitors exhibit ICsu

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