Cas 1164102-75-3,(E)-1-(4-(3H-pyrrolo[3,2-f]quinolin-9-ylamino)phenyl)-3-(1H-pyrrol-2-yl)prop-2-en-1-one

1164102-75-3

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Basic information

Product Name: (E)-1-(4-(3H-pyrrolo[3,2-f]quinolin-9-ylamino)phenyl)-3-(1H-pyrrol-2-yl)prop-2-en-1-one
Synonyms:
CAS NO:1164102-75-3
Molecular Formula:
Molecular Weight: 378.433
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: (E)-1-(4-(3H-pyrrolo[3,2-f]quinolin-9-ylamino)phenyl)-3-(1H-pyrrol-2-yl)prop-2-en-1-one(CAS DataBase Reference)
NIST Chemistry Reference: (E)-1-(4-(3H-pyrrolo[3,2-f]quinolin-9-ylamino)phenyl)-3-(1H-pyrrol-2-yl)prop-2-en-1-one(1164102-75-3)
EPA Substance Registry System: (E)-1-(4-(3H-pyrrolo[3,2-f]quinolin-9-ylamino)phenyl)-3-(1H-pyrrol-2-yl)prop-2-en-1-one(1164102-75-3)

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: 1164102-75-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1164102-75-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,6,4,1,0 and 2 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1164102-75:
(9*1)+(8*1)+(7*6)+(6*4)+(5*1)+(4*0)+(3*2)+(2*7)+(1*5)=113
113 % 10 = 3
So 1164102-75-3 is a valid CAS Registry Number.

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1164102-75-3Relevant academic research and scientific papers

DNA-targeting pyrroloquinoline-linked butenone and chalcones: Synthesis and biological evaluation

Via, Lisa Dalla,Gia, Ornella,Chiarelotto, Gianfranco,Ferlin, Maria Grazia

experimental part, p. 2854 - 2861 (2009/10/10)

A series of conjugates of α,β-unsaturated ketone systems, phenyl-butenone and diaryl-propenones (chalcones), with the tricyclic planar pyrroloquinoline nucleus were synthesised and evaluated for their anticancer properties. The aim was to target DNA by bu

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