4707-71-5 Usage
Description
PHENANTHRENE-9-CARBOXALDEHYDE, also known as a phenanthrene derivative, is a pale yellow powder with unique chemical properties. It is characterized by its ability to be synthesized into various fluorescent probes, making it a valuable compound in the field of chemical research and development.
Uses
Used in Chemical Research and Development:
PHENANTHRENE-9-CARBOXALDEHYDE is used as a starting material for the synthesis of fluorescent probes due to its unique chemical properties and reactivity.
Used in Analytical Chemistry:
PHENANTHRENE-9-CARBOXALDEHYDE is used as a component in the creation of fluorescent probes for analytical chemistry applications, such as detecting and analyzing specific molecules or ions in complex samples.
Used in Biomedical Research:
In the field of biomedical research, PHENANTHRENE-9-CARBOXALDEHYDE is used as a building block for the development of fluorescent probes that can be employed in cellular imaging, drug discovery, and the study of biological processes.
Used in Environmental Science:
PHENANTHRENE-9-CARBOXALDEHYDE is utilized in the production of fluorescent probes for environmental science applications, including the detection and monitoring of pollutants and contaminants in various ecosystems.
Used in Material Science:
PHENANTHRENE-9-CARBOXALDEHYDE is employed in the development of fluorescent probes for material science, where they can be used to study the properties and behavior of new materials and their potential applications in various industries.
Purification Methods
Crystallise the aldehyde from EtOH and sublime it at 95-98o/0.07mm. The 2,4-dinitrophenylhydrazone has m 272-273o. [Beilstein 7 III 2532, 7 IV 1740.]
Check Digit Verification of cas no
The CAS Registry Mumber 4707-71-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,7,0 and 7 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4707-71:
(6*4)+(5*7)+(4*0)+(3*7)+(2*7)+(1*1)=95
95 % 10 = 5
So 4707-71-5 is a valid CAS Registry Number.
InChI:InChI=1/C15H10O/c16-10-12-9-11-5-1-2-6-13(11)15-8-4-3-7-14(12)15/h1-10H
4707-71-5Relevant articles and documents
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Hewett
, p. 193,195 (1938)
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Bifunctional antitumor agents. Derivatives of pyrrolo[9,10-b]phenanthrene - A DNA intercalative delivery template
Jones, Graham B.,Mathews, Jude E.
, p. 14599 - 14614 (1997)
The preparation and intercalative ability of the pyrrolo[9,10-b]phenanthrene nucleus is described. Functionalization of the nucleus was achieved using standard indole chemistry. The utility of this template as a DNA intercalating drug delivery system is demonstrated by synthesis of a derived bis-chloroethylamine alkylating system and a hybrid DNA interactive enediyne system.
Microwave-assisted Vilsmeier-Haack formylation of aromatic substrates
Ghosh, Kumaresh,Adhikari, Suman
experimental part, p. 959 - 961 (2009/12/24)
A microwave-assisted Vilsmeier-Haack formylation reaction has been studied on various amines, phenols and polynuclear hydrocarbons under solvent free condition that rapidly affords higher yield of products compared to traditional thermal condition.
Therapeutics for chemokine mediated diseases
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, (2008/06/13)
The invention provides therapeutic and biological uses of chemokine-receptor-binding compounds (including chemokine receptor ligands such as chemokine receptor agonists or antagonists), such as tricyclic phenanthrene derivatives, including uses in the treatment of disease states mediated by chemokines. The relevant chemokines may for example be monocyte chemoattractant protein-one (MCP-1) or interleukin-8 (IL-8), and the relevant chemokine receptors may for example be corresponding chemokine receptors (CCR-2, CCR-4, CXCR-1, and CXCR-2). In other aspects, the invention provides corresponding pharamaceutical compositions and therapeutic methods. In one aspect, for example, the invention provides for the use of phenanthrene-9,10-dione in the treatment of multiple sclerosis.
