343372-28-1 Usage
Structure
Cyclic formation with氧, 硫, 氮, and 碳 atoms The compound has a unique structure with a ring-like shape formed by the arrangement of these atoms.
Complexity
Diverse applications The structural complexity of the compound suggests it may have various applications in fields such as pharmaceuticals, materials science, and chemical synthesis.
Chemical properties
Range of properties 1-OXA-4,10,16-TRITHIA-7,13-DIAZACYCLOOCTADECANE is likely to exhibit multiple chemical properties due to its complex structure.
Biological activities
Potential The compound may have various biological activities, which could make it useful in the development of new drugs or therapies.
Research and exploration
Warranted Further investigation is needed to fully understand the capabilities and limitations of this intriguing compound and its potential uses.
Check Digit Verification of cas no
The CAS Registry Mumber 343372-28-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,3,3,7 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 343372-28:
(8*3)+(7*4)+(6*3)+(5*3)+(4*7)+(3*2)+(2*2)+(1*8)=131
131 % 10 = 1
So 343372-28-1 is a valid CAS Registry Number.
343372-28-1Relevant articles and documents
Bis-8-hydroxyquinoline-armed diazatrithia-15-crown-5 and diazatrithia-16-crown-5 ligands: Possible fluorophoric metal ion sensors
Bronson,Bradshaw,Savage,Fuangswasdi,Sang Chul Lee,Krakowiak,Izatt
, p. 4752 - 4758 (2007/10/03)
The synthesis and preliminary photophysical properties of a series of diazatrithia-15-crown-5 and diazatrithia-16-crown-5 ligands containing two 8-hydroxyquinoline sidearms are reported. The ligands were prepared by a two-step process. First, diazatrithiacrown ethers 11 and 12 were prepared by treating bis(α-chloroamide) 5 with various dimercaptans followed by reduction using a boron-THF complex. Hydroxymethyl-substituted macrocycle 12 was rearranged to hydroxy-substituted diazatrithia-16-crown-5 in refluxing aqueous HCl. Macrocyclic diamines 11-13 were converted to either 5-chloro-8-hydroxyquinolin-7-ylmethyl-substituted diazatrithiacrown ethers 14-16 by a Mannich aminomethylation reaction or to 8-hydroxyquinolin-2-ylmethyl-substituted diazatrithiacrown ethers 17-19 by reductive amination using 8-hydroxyquinoline-2-carboxaldehyde. Preliminary photophysical studies show that ligands 16 and 19 exhibit increased fluorescence in the presence of Zn2+, indicating that these ligands could be chemical sensors for Zn2+.
