316124-91-1 Usage
Description
ETHYL 2-(2-ISOBUTYL-6-QUINOLYLOXY-8-P-TOLUENESULFONAMIDO)ACETATE is a complex organic compound with a chemical structure that features a quinoloxy group, an isobutyl group, and a p-toluenesulfonamido group attached to an ethyl acetate backbone. It is characterized by its white solid appearance and exhibits unique chemical properties that make it suitable for various applications in different industries.
Uses
Used as a Fluorescent Reagent:
ETHYL 2-(2-ISOBUTYL-6-QUINOLYLOXY-8-P-TOLUENESULFONAMIDO)ACETATE is used as a fluorescent reagent in the field of biochemistry and molecular biology. Its fluorescent properties allow researchers to track and visualize specific biological processes, making it a valuable tool for studying cellular mechanisms and interactions.
Used as an Indicator of Intracellular Zinc Ions:
In the field of cellular biology, ETHYL 2-(2-ISOBUTYL-6-QUINOLYLOXY-8-P-TOLUENESULFONAMIDO)ACETATE serves as an indicator for intracellular zinc ions. Zinc is an essential trace element that plays a crucial role in various cellular functions, including enzyme activity, gene expression, and cellular signaling. By using this compound as an indicator, researchers can monitor and measure the levels of zinc ions within cells, providing valuable insights into zinc-related processes and their potential impact on cell health and function.
Used in Pharmaceutical Industry:
ETHYL 2-(2-ISOBUTYL-6-QUINOLYLOXY-8-P-TOLUENESULFONAMIDO)ACETATE may also find applications in the pharmaceutical industry, where its unique chemical structure could be harnessed for the development of new drugs or drug delivery systems. Its potential use in this industry could be related to its ability to interact with specific biological targets or its capacity to enhance the efficacy of existing medications.
Used in Chemical Research and Development:
Due to its complex structure and unique properties, ETHYL 2-(2-ISOBUTYL-6-QUINOLYLOXY-8-P-TOLUENESULFONAMIDO)ACETATE can be utilized in chemical research and development. It may serve as a starting material or intermediate in the synthesis of other complex organic compounds, contributing to the advancement of chemical science and technology.
Check Digit Verification of cas no
The CAS Registry Mumber 316124-91-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,1,6,1,2 and 4 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 316124-91:
(8*3)+(7*1)+(6*6)+(5*1)+(4*2)+(3*4)+(2*9)+(1*1)=111
111 % 10 = 1
So 316124-91-1 is a valid CAS Registry Number.
316124-91-1Relevant articles and documents
The synthesis and fluorescent properties of analogues of the zinc(II) specific fluorophore zinquin ester
Kimber,Mahadevan,Lincoln,Ward,Tiekink
, p. 8204 - 8209 (2007/10/03)
The synthesis and fluorescent properties in the absence and presence of zinc(II) of a range of 2-substituted derivatives of N-(6-methoxy-2-methyl-8-quinolyl)-4-methylbenzenesulfonamide are described. These analogues formed complexes with zinc(II) as indicated by a bathochromic shift in their UV/vis spectra. Analogues with isobutenyl and isobutyl side chains at the 2-position formed fluorescent complexes whose fluorescence was stronger than that of the 2-methyl-containing parent. These derivatives were converted, via conversion to the phenol with boron tribromide and reaction with ethyl bromoacetate, to systems with ester-containing side chains analogous to zinquin ester, a specific cellular fluorophore for zinc(II). All of these ester derivatives formed complexes with zinc(II) resulting in a bathochomic shift in their UV/vis spectra. Compounds with isobutyl, isobutenyl, and styryl side chains exhibited increased fluorescence compared to that of zinquin ester in the presence of zinc(II). The compound with the 2-isobutyl side chain was more selective in its fluorescence for zinc(II) over cadmium(II) compared to zinquin ester.
