| Company Name: |
CHEMICAL LAND21
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82- 2 -783 - 8063 |
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sales21@chemicalland21.com |
| Products Intro: |
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| | Chlorquinox Basic information |
| Product Name: | Chlorquinox | | Synonyms: | Lucel;5,6,7,8-TETRACHLOROQUINOXALINE;Quinoxaline, 5,6,7,8-tetrachloro- | | CAS: | 3495-42-9 | | MF: | C8H2Cl4N2 | | MW: | 267.93 | | EINECS: | | | Product Categories: | | | Mol File: | 3495-42-9.mol |  |
| | Chlorquinox Chemical Properties |
| Melting point | 190°C | | Boiling point | 416.98°C (rough estimate) | | density | 1.8206 (rough estimate) | | refractive index | 1.6000 (estimate) | | pka | -4.56±0.30(Predicted) | | Water Solubility | 1mg/L(25 ºC) | | EPA Substance Registry System | Chlorquinox (3495-42-9) |
| | Chlorquinox Usage And Synthesis |
| Description | Chlorquinox is an obsolete fungicide that was used to control powdery mildew. The chemical has not been extensively studied and there is little available information. The substance is moderately toxic to birds and has a low mammalian toxicity. | | Production Methods | Chlorquinox production would begin with a 1,2 phenylenediamine derivative, which is condensed with a tetrachloro substituted 1,2 dicarbonyl compound to form the quinoxaline heterocycle. This cyclocondensation reaction, typical for quinoxaline synthesis, proceeds under acidic or thermal conditions, after which the crude compound is purified by solvent extraction and recrystallisation to yield technical grade chlorquinox. | | Definition | ChEBI: A quinoxaline antifungal agent that is quinoxaline in which the hydrogens at positions 5, 6, 7, and 8 are replaced by chlorines. Chlorquinox was developed in the 1970s and was used on crops for the control of powdery mildew; it is now obsolete. | | Mechanism of action | Multi-site contact activity. Disrupts fungal respiration, targeting complex II of the mitochondrial electron transport chain preventing the fungus from generating energy | | Pesticide Type | Fungicide |
| | Chlorquinox Preparation Products And Raw materials |
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