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AgrochemicalsBromoxynil Impurity 2

SKU: SAB-09-B

Original price was: ₹60,000.00.Current 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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