Cas 630414-76-5,7-Quinolinecarboxamide, N-[2-[bis[2-[(2,3-dihydroxybenzoyl)amino]ethyl]amino]ethyl]-8-hydroxy-

630414-76-5

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Basic information

Product Name: 7-Quinolinecarboxamide, N-[2-[bis[2-[(2,3-dihydroxybenzoyl)amino]ethyl]amino]ethyl]-8-hydroxy-
Synonyms:
CAS NO:630414-76-5
Molecular Formula: C30H31N5O8
Molecular Weight: 589.605
EINECS: N/A
Product Categories: N/A
Mol File: 630414-76-5.mol
Article Data: 1

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: 7-Quinolinecarboxamide, N-[2-[bis[2-[(2,3-dihydroxybenzoyl)amino]ethyl]amino]ethyl]-8-hydroxy-(CAS DataBase Reference)
NIST Chemistry Reference: 7-Quinolinecarboxamide, N-[2-[bis[2-[(2,3-dihydroxybenzoyl)amino]ethyl]amino]ethyl]-8-hydroxy-(630414-76-5)
EPA Substance Registry System: 7-Quinolinecarboxamide, N-[2-[bis[2-[(2,3-dihydroxybenzoyl)amino]ethyl]amino]ethyl]-8-hydroxy-(630414-76-5)

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: 630414-76-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 630414-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,3,0,4,1 and 4 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 630414-76:
(8*6)+(7*3)+(6*0)+(5*4)+(4*1)+(3*4)+(2*7)+(1*6)=125
125 % 10 = 5
So 630414-76-5 is a valid CAS Registry Number.

630414-76-5Upstream product

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630414-76-5Relevant articles and documents

Iron(III) chelation: Tuning of the pH dependence by mixed ligands

Albrecht-Gary, Anne-Marie,Blanc, Sylvie,Biaso, Frederic,Thomas, Fabrice,Baret, Paul,Gellon, Gisele,Pierre, Jean-Louis,Serratrice, Guy

, p. 2596 - 2605 (2007/10/03)

The iron(III) chelating properties of two heteropodands with 8-hydroxyquinoline and catechol binding groups were examined and compared to those of the corresponding homopodal analogues, O-TRENSOX and TRENCAMS. Like the parent homopodands, the two heteropo

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