CAS 28343-61-5
:4-Hydroxy-2,5,6-trichloroisophthalonitrile
Description:
4-Hydroxy-2,5,6-trichloroisophthalonitrile, with the CAS number 28343-61-5, is a chemical compound characterized by its structure, which includes a hydroxyl group and multiple chlorine substituents on an isophthalonitrile framework. This compound typically appears as a solid and is known for its stability under various conditions. It exhibits properties such as high thermal stability and resistance to degradation, making it suitable for applications in materials science, particularly in the development of flame retardants and polymers. The presence of chlorine atoms contributes to its reactivity and potential use in synthesis, while the hydroxyl group can participate in hydrogen bonding, influencing its solubility and interaction with other substances. Additionally, due to its nitrile groups, it may exhibit certain toxicological properties, necessitating careful handling and assessment in industrial applications. Overall, 4-Hydroxy-2,5,6-trichloroisophthalonitrile is a compound of interest in both research and practical applications, particularly in the fields of chemistry and materials engineering.
Formula:C8HCl3N2O
InChI:InChI=1/C8HCl3N2O/c9-5-3(1-12)6(10)7(11)8(14)4(5)2-13/h14H
InChI key:InChIKey=MDQKYGOECVSPIW-UHFFFAOYSA-N
SMILES:C(#N)C1=C(Cl)C(C#N)=C(O)C(Cl)=C1Cl
Synonyms:- 1,3-Benzenedicarbonitrile, 2,4,5-Trichloro-6-Hydroxy-
- 1,3-Dicyano-4-Hydroxy-2,5,6-Trichlorobenzene
- 2,4,5-Trichloro-6-hydroxy-1,3-benzenedicarbonitrile
- 2,4,5-Trichloro-6-hydroxyisophthalonitrile
- 2,5,6-Trichloro-4-hydroxy-1,3-benzenedicarbonitrile
- 28343-61-5
- 4-Hydroxy-2,5,6-trichloroisophthalonitrile
- 4-Hydroxychlorothalonil
- Hydroxychlorothalonil
- Isophthalonitrile, 2,4,5-trichloro-6-hydroxy-
- Sds 3701
- 2,5,6-Trichloro-4-
- Hydroxy Chlorothalonil Q: What is the storage condition of
- Hydroxy Chlorothalonil Q: What is the CAS Number of
- 2,4,5-Trichloro-6-hydroxy-
- Hydroxy Chlorothalonil
- Tribenoside Impurity 6
- Chlorothalonil Metabolite R182281
- hydroxy-1,3-benzenedicarbonitrile
- 4-hydroxy-2,5,6-trichloro-1,3-benzenedicarbonitrile
- Hydroxy ChlorothalonilQ: What is
- 4-hydroxy-2,5,6-trichloro-3-benzenedicarbonitrile
- Hydroxy Chlorothalonil Q: What are the applications of
- TPN-OH
- DRE-C11510400 Chlorothalonil-4-hydroxy
- isophthalonitrile
- Chlorothalonil-4-hydroxy 10.0 μg/ml Acetonitrile
- See more synonyms
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Found 5 products.
Chlorothalonil-4-hydroxy 10 µg/mL in Acetonitrile
CAS:Formula:C8HCl3N2OColor and Shape:ColourlessMolecular weight:247.47Chlorothalonil-4-hydroxy
CAS:Controlled ProductFormula:C8HCl3N2OColor and Shape:NeatMolecular weight:247.47Hydroxy Chlorothalonil
CAS:Controlled Product<p>Applications Hydroxychlorothalonil is a metabolite of Chlorothalonil (C411250).<br> Not a dangerous good if item is equal to or less than 1g/ml and there is less than 100g/ml in the package<br>References Katayama, A., et al.: J. Pest Sci., 22, 12 (1997), Godard, T., et al.: Mutat. Res., 444, 103 (1999), Zeng, L., et al.: Appl. Microbiol. Biotechnol., 79, 881 (2008), Wang, G., et al.: J. Bacteriol., 192, 2737 (2010),<br></p>Formula:C8HCl3N2OColor and Shape:Off-WhiteMolecular weight:247.472,4,5-Trichloro-6-hydroxyisophthalonitrile
CAS:<p>2,4,5-Trichloro-6-hydroxyisophthalonitrile is a fungicide. It is used in the control of plant diseases such as powdery mildew, rust and blight. 2,4,5-Trichloro-6-hydroxyisophthalonitrile can be applied to plants through foliar spray or root drenching. It acts by inhibiting the enzyme activities of fungi that are responsible for cell growth. This compound has been shown to have genotoxic activity in vivo and in vitro models and may be carcinogenic to humans. The mechanism of action of 2,4,5-trichloro-6-hydroxyisophthalonitrile remains unclear due to its high resistance to degradation in vivo. 2,4,5-Trichloro-6-hydroxyisophthalonitrile has also shown synergistic effects when combined with zirconium oxide and matrix</p>Formula:C8HCl3N2OPurity:Min. 95%Molecular weight:247.47 g/mol



