Cas 877475-78-0,2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[4-(4-aminophenyl)-1-piperazinyl]-5-[1,1'-biphenyl]-4-yl-

877475-78-0

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Basic information

Product Name: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[4-(4-aminophenyl)-1-piperazinyl]-5-[1,1'-biphenyl]-4-yl-
Synonyms:
CAS NO:877475-78-0
Molecular Formula: C26H25N5O3
Molecular Weight: 455.516
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: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[4-(4-aminophenyl)-1-piperazinyl]-5-[1,1'-biphenyl]-4-yl-(CAS DataBase Reference)
NIST Chemistry Reference: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[4-(4-aminophenyl)-1-piperazinyl]-5-[1,1'-biphenyl]-4-yl-(877475-78-0)
EPA Substance Registry System: 2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-[4-(4-aminophenyl)-1-piperazinyl]-5-[1,1'-biphenyl]-4-yl-(877475-78-0)

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: 877475-78-0(Hazardous Substances Data)

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877475-78-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 877475-78-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,7,4,7 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 877475-78:
(8*8)+(7*7)+(6*7)+(5*4)+(4*7)+(3*5)+(2*7)+(1*8)=240
240 % 10 = 0
So 877475-78-0 is a valid CAS Registry Number.

877475-78-0Upstream product

877475-78-0Downstream Products

877475-78-0Relevant academic research and scientific papers

5-(1,1'-BIPHENYL)-4-YL-5-(4-(4-AMINOACYLPHENYL)-PIPERAZIN)-1-YL-PYRIMIDINE-2,4,6-TRIONE DERIVATIVES, AS INHIBITORS OF ZINC METALLONDOPEPTIDASES, THEIR PREPARATION AND USE

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Page/Page column 10, (2008/06/13)

New Pyrimidinetrione derivatives represented by formula (I), wherein R1 and R2 are defined in the description, composition thereof, and methods of preparation are described. The compounds are useful in the treatment of disease involving metalloproteinases.

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