6962-88-5 Usage
Primary Use
Fluorescent probe for detecting and quantifying zinc ions in biological systems
Selectivity
High selectivity and sensitivity towards zinc ions
Structure
Consists of a boronate group linked to a naphthalene ring
Binding Mechanism
Efficient binding and sensing of zinc ions facilitated by its unique structure
Applications
Widely used in research and clinical settings to monitor zinc levels in cells and tissues
Potential
Promising for the development of new diagnostic and therapeutic strategies for zinc-related disorders
Check Digit Verification of cas no
The CAS Registry Mumber 6962-88-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,6 and 2 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6962-88:
(6*6)+(5*9)+(4*6)+(3*2)+(2*8)+(1*8)=135
135 % 10 = 5
So 6962-88-5 is a valid CAS Registry Number.
6962-88-5Relevant articles and documents
Synthesis and anticoccidial activity of some azacyclo organoborinates
Tabuchi, Hitoshi,Kawaguchi, Harumoto,Taniguchi, Hisashi,Imazaki, Hideyuki,Hayase, Yoshio
, p. 1319 - 1326 (2007/10/03)
A series of azacyclo organoborinates derivatives of piperidinyl and pyridinyl alcohols were prepared and their anticoccidial activity was tested in vitro assay system. Among them, di(4-chlorophenyl)(2-piperidinylmethoxy-O,N)boron, di(3-trifluoromethylphenyl)(2-piperidinylmethoxy-O,N)boron, di(3-trifluoromethylphenyl)(2-pyridinylmethoxy-O,N)boron, and di(3-trifluoromethylphenyl)(2-pyridinylethoxy-O,N)boron, showed moderate anticoccidial activity against Eimeria tenella.