33155-90-7 Usage
Uses
Used in Chemical Sensing:
10-Hydroxybenzo[h]quinoline is used as a chemical sensor for detecting boronic acids in reactions and identifying boron-containing compounds on solid support. Its sensitivity and selectivity make it a valuable tool in the field of chemical analysis.
Used in Fluorescence Probing:
In the field of biochemistry, 10-Hydroxybenzo[h]quinoline serves as a proton transfer-fluorescence probe. It is applied to human serum albumin and beaver apomyoglobin, allowing for the study of protein interactions and structural changes at a molecular level.
Used in Pharmaceutical Research:
10-Hydroxybenzo[h]quinoline's unique chemical properties also make it a promising candidate for pharmaceutical research. Its potential applications in drug development and design are currently being explored, with a focus on its ability to interact with various biological targets.
Used in Material Science:
10-Hydroxybenzo[h]quinoline's light yellow solid form and chemical properties make it a candidate for use in the development of new materials with specific optical, electronic, or mechanical properties. It may be utilized in the creation of advanced materials for various applications, such as sensors, displays, or energy storage devices.
Used in Environmental Monitoring:
10-Hydroxybenzo[h]quinoline's ability to detect boron-containing compounds can also be applied in environmental monitoring. It can be used to analyze and monitor the presence of boron in water, soil, and air samples, contributing to the assessment of environmental contamination and the development of remediation strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 33155-90-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,5 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33155-90:
(7*3)+(6*3)+(5*1)+(4*5)+(3*5)+(2*9)+(1*0)=97
97 % 10 = 7
So 33155-90-7 is a valid CAS Registry Number.
InChI:InChI=1/C13H9NO/c15-11-5-1-3-9-6-7-10-4-2-8-14-13(10)12(9)11/h1-8,15H
33155-90-7Relevant academic research and scientific papers
Temperature-controlled acyloxylations and hydroxylations of bromoarene by a silver salt
Yoo, Kwangho,Park, Hyojin,Kim, Suyeon,Kim, Min
supporting information, p. 781 - 783 (2016/02/03)
Temperature-controlled selective acyloxylations and hydroxylations of bromoarene were achieved using a silver salt. Various aryl esters were synthesized at 100°C, and the hydroxylated arene was obtained at 150°C from silver-mediated conditions. Mechanistically, a two-step acyloxylation-hydrolysis pathway was revealed for hydroxylation of bromoarene.
Studies into the generation and Diels-Alder reactions of 7,8-quinolyne with furan dienes
Collis, Gavin E.,Burrell, Anthony K.
, p. 3653 - 3656 (2007/10/03)
Reaction of an appropriate ortho-halo tosylate precursor with organolithium reagents provides the first conclusive route to the intermediate, 7,8-quinolyne. The transient existence of this hetaryne was confirmed by Diels-Alder reactions with furan derivatives that provide endoxide adducts. Chemical induced rearrangement of these adducts allows entry to key compounds of 10-hydroxy[h]benzoquinoline and its 7-substituted derivatives in modest yields.
