9-Chloroacridine
9-Chloroacridine structure
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Common Name | 9-Chloroacridine | ||
|---|---|---|---|---|
| CAS Number | 1207-69-8 | Molecular Weight | 213.662 | |
| Density | 1.3±0.1 g/cm3 | Boiling Point | 379.4±15.0 °C at 760 mmHg | |
| Molecular Formula | C13H8ClN | Melting Point | 116-120 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 215.2±6.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Designed Intercalators for Modification of DNA Origami Surface Properties.
Chemistry 21 , 9440-6, (2015) The modification of the backbone properties of DNA origami nanostructures through noncovalent interactions with designed intercalators, based on acridine derivatized with side chains containing esterified fatty acids or oligo(ethylene glycol) residues is repo... |
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Arylethynylacridines: electrochemiluminescence and photophysical properties.
Org. Biomol. Chem. 2(21) , 3113-8, (2004) Electrogenerated chemiluminescence (ECL) of six new ethyne-based acridine derivatives (1-6) has been studied. The new acridine derivatives were synthesized by cross-coupling of 9-chloroacridine and corresponding donor-substituted phenylethynes under modified ... |
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Synthesis of new chalcone derivatives containing acridinyl moiety with potential antimalarial activity.
Eur. J. Med. Chem. 45(2) , 745-51, (2010) A series of novel chalcones bearing acridine moiety attached to the amino group in their ring A have been synthesized through noncatalyzed nucleophilic aromatic substitution reaction between various 3'-aminochalcone or 4'-aminochalcones and 9-chloroacridine. ... |
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Synthesis and anti-inflammatory evaluation of 9-phenoxyacridine and 4-phenoxyfuro[2,3-b]quinoline derivatives. Part 2.
Bioorg. Med. Chem. 11(18) , 3921-7, (2003) Mast cells, neutrophils and macrophages are important inflammatory cells that have been implicated in the pathogenesis of acute and chronic inflammatory diseases. To explore a novel anti-inflammatory agent, we have synthesized certain 9-phenoxyacridine and 4-... |
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Spectrophotometric determination of dapsone by using 9-chloroacridine as a chromogenic reagent.
Pharmazie 45(9) , 675-7, (1990) A spectrophotometric method for the quantitative determination of dapsone (1) has been developed through a condensation reaction of 9-chloroacridine as a chromogen and the amino groups of 1. The reaction variables were investigated and optimized. The resultan... |