AgrochemicalsBromoxynil Impurity 2
Original price was: ₹60,000.00.₹50,000.00Current price is: ₹50,000.00.
Bromoxynil Impurity 2
Name:3,5-Diiodo-4-hydroxybenzonitrile
CAT. NO.:SAB-09-B
CAS NO.:1689-83-4
- Description
- Datasheet
- Additional information
Description
Bromoxynil Impurity 2
Chemical Name | 3,5-Diiodo-4-hydroxybenzonitrile |
Catalog Number | SAB-09-B |
Parent AI | Bromoxynil |
Synonyms | 2,6-Diiodo-4-cyanophenol; 3,5-Diiodo-4-hydroxybenzonitrile; 4-Cyano-2,6-diiodophenol; 4-Hydroxy-3,5-diiodobenzonitrile; Actril; Bentrol; CA 69-15; Certrol; Cipotril; Exp 30004A; Ioksynil; Ioxynil; Joxynil; MB 8873; Toxynil; Trevespan |
CAS Number | 1689-83-4 |
Molecular Formula | C₇H₃I₂NO |
Molecular Weight | 370.91 |
Appearance | Solid powder |
Melting Point | 212.5 °C |
Shipping & Storage Information
 |
Storage-20°C
Shipping: Free Shipping at Room Temperature in INDIA, may vary elsewhere Stability: Datasheet |
Solubility | SLIGHTLY SOL IN CHLOROFORM; SOL IN ETHER AT 25 °C |
Stability | Stable under recommended storage conditions |
Category | Agrochemical Impurity Standard/Metabolites |
Description &Applications | Ioxynil is a post-emergent herbicide, which can be used to selectively control broad-leaved weeds in cereals and grass crops. It can be used in combination with phenoxy herbicides in order to control hormone-resistant weeds. Ioxynil is a nitrile that is benzonitrile substituted by a hydroxy group at position 4 and iodo groups at positions 3 and 5. It has a role as a xenobiotic, an environmental contaminant and a herbicide. It is a nitrile and an iodophenol. |
References | Andreasen, C., et al.: Weed Res., 46, 503 (2006), Mithila, J., et al.: Weed Sci., 56, 12 (2008) |
3,5-Diiodo-4-hydroxybenzonitrile. This compound, with its distinctive arrangement of atoms and functional groups, presents a captivating canvas for exploration and innovation across various scientific disciplines.
Chemical Structure and Properties: At first glance, 3,5-Diiodo-4-hydroxybenzonitrile might appear as a mere arrangement of atoms and bonds. However, delving into its structural intricacies reveals a tale of chemical interactions and potential reactivity. The compound consists of a benzene ring with two iodine atoms occupying the 3rd and 5th positions, and a hydroxy (-OH) group and a nitrile (-CN) group situated at the 4th position. This unique arrangement not only lends the molecule its distinctive characteristics but also opens doors to a wide array of applications.
The presence of iodine atoms in the molecule imparts a degree of polarity and reactivity, rendering 3,5-Diiodo-4-hydroxybenzonitrile a promising candidate for diverse chemical transformations. Its hydroxy and nitrile groups further enhance its potential for involvement in various reaction pathways, making it a valuable building block in synthetic chemistry.
Synthetic Applications: The synthesis of 3,5-Diiodo-4-hydroxybenzonitrile is a testament to the creativity and ingenuity of chemists. It serves as a precursor to an assortment of compounds with applications ranging from pharmaceuticals to materials science. Chemists can harness its unique attributes to create complex molecular architectures that are essential for drug discovery, agrochemicals, and advanced materials.
In the pharmaceutical realm, the compound’s structural features make it an attractive candidate for medicinal chemistry. It can serve as a key intermediate in the synthesis of novel pharmaceutical agents, capitalizing on its iodine atoms for radio-labeled compounds used in positron emission tomography (PET) imaging. Furthermore, its hydroxy group could be exploited for introducing hydrogen bonding interactions, potentially enhancing drug-receptor interactions.
Material Science and Beyond: The versatility of 3,5-Diiodo-4-hydroxybenzonitrile extends beyond pharmaceuticals into the realm of materials science. Researchers have begun to explore its potential in designing functional materials with tailored properties. By incorporating this compound into polymer matrices, for instance, scientists can engineer materials with enhanced thermal stability, conductivity, or mechanical strength. The presence of iodine atoms could also offer opportunities for tuning material properties through halogen bonding interactions, an emerging concept in supramolecular chemistry.
Additional information
Pack Size | 50mg |
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