1240642-73-2 Usage
Uses
Used in Organic Synthesis:
5-Amino-6-bromo-1-naphthonitrile is used as a building block in organic synthesis for its ability to participate in various chemical reactions, facilitating the creation of a broad spectrum of organic compounds.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 5-Amino-6-bromo-1-naphthonitrile is utilized as an intermediate in the synthesis of pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemicals:
5-Amino-6-bromo-1-naphthonitrile is also employed in the synthesis of agrochemicals, playing a role in the development of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Biological Research:
5-aMino-6-broMo-1-naphthonitrile is used as a fluorescent probe in biological research, particularly in cell imaging and biochemical assays, due to its potential biological activities and fluorescent properties, which allow for the tracking and analysis of cellular processes.
Used in Fluorescent Probes for Imaging:
5-Amino-6-bromo-1-naphthonitrile is utilized in the development of fluorescent probes for imaging applications, taking advantage of its fluorescent characteristics to visualize and study biological structures and functions within cells and tissues.
Check Digit Verification of cas no
The CAS Registry Mumber 1240642-73-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,0,6,4 and 2 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1240642-73:
(9*1)+(8*2)+(7*4)+(6*0)+(5*6)+(4*4)+(3*2)+(2*7)+(1*3)=122
122 % 10 = 2
So 1240642-73-2 is a valid CAS Registry Number.
1240642-73-2Relevant academic research and scientific papers
Yang, Youjun,Seidlits, Stephanie K.,Adams, Michelle M.,Lynch, Vincent M.,Schmidt, Christine E.,Anslyn, Eric V.,Shear, Jason B.
, p. 13114 - 13116 (2010)
We introduce a novel sensing mechanism for nitric oxide (NO) detection with a particular easily synthesized embodiment (NO550), which displays a rapid and linear response to NO with a red-shifted 1500-fold turn-on signal from a dark background. Excellent selectivity was observed against other reactive oxygen/nitrogen species, pH, and various substances that interfere with existing probes. NO550 crosses cell membranes but not nuclear membranes and is suitable for both intra-and extracellular NO quantifications. Good cytocompatibility was found during in vitro studies with two different cell lines. The high specificity, dark background, facile synthesis, and low pH dependence make NO550 a superior probe for NO detection when used as an imaging agent.
FLUORESCENT NITRIC OXIDE PROBES AND ASSOCIATED METHODS
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Paragraph 0056; 0057, (2013/11/19)
Nitric oxide probes comprising a compound represented by Formula, I, II, III, IV, V, VI or a combination thereof are provided. Methods of using these nitric oxide probes to detect nitric oxide are also provided.
