AgrochemicalsBensuliden Impurity 2
Original price was: ₹60,000.00.₹50,000.00Current price is: ₹50,000.00.
Bensuliden Impurity 2
Name:N-(2-Chloroethyl)benzenesulfonamide
CAT. NO.:SAB-05-B
CAS NO.:6453-86-7
- Description
- Datasheet
- Additional information
Description
Bensuliden Impurity 2
Chemical Name | N-(2-Chloroethyl)benzenesulfonamide |
Catalog Number | SAB-05-B |
Parent AI | Bensulide |
Synonyms | NA |
CAS Number | 6453-86-7 |
Molecular Formula | C₈H₁₀ClNO₂S |
Molecular Weight | 219.69 |
Appearance | White Solid |
Melting Point | NA |
Shipping & Storage Information
|
Storage 20°C
Shipping: Free Shipping at Room Temperature in INDIA, may vary elsewhere Stability: Datasheet |
Solubility | Chloroform |
Stability | Stable under recommended storage conditions |
Category | Building Blocks; Miscellaneous; |
Description &Applications | N-(2-Chloroethyl)benzenesulfonamide is an intermediate for the synthesis of Bensulide (B166000), which is an organophosphate acetylcholinesterase inhibitor used as an herbicide (1) in the protection of crops through pesticides (2). Drinking water contaminant candidate list 3 (CCL 3) compound as per United States Environmental Protection Agency (EPA), environmental, and food contaminants. |
N-(2-Chloroethyl)benzenesulfonamide is a versatile organic compound that finds applications in various fields, including pharmaceuticals, agrochemicals, and materials science. This chemical compound is known for its unique structure and functional groups, which contribute to its diverse range of uses. In this article, we will delve into the synthesis, properties, and applications of N-(2-Chloroethyl)benzenesulfonamide.
Synthesis: The synthesis of N-(2-Chloroethyl)benzenesulfonamide involves the introduction of a chloroethyl group onto a benzene ring bearing a sulfonamide functional group. This can be achieved through several synthetic routes, one of which involves the reaction of benzenesulfonamide with 2-chloroethanol in the presence of a suitable catalyst. The reaction typically takes place under controlled conditions, resulting in the formation of the desired compound. Careful purification and characterization processes ensure the quality and purity of the final product.
Properties: N-(2-Chloroethyl)benzenesulfonamide exhibits interesting physical and chemical properties that make it valuable for various applications. The compound is typically a white to off-white crystalline solid, and its solubility in different solvents allows for versatility in its usage. It is stable under ambient conditions, although it may undergo specific reactions under controlled circumstances. The presence of both a chloroethyl group and a sulfonamide functional group offers opportunities for various chemical modifications, enhancing its applicability in diverse fields.
Applications:
- Pharmaceuticals: N-(2-Chloroethyl)benzenesulfonamide serves as a building block in the synthesis of various pharmaceutical compounds. Its ability to participate in diverse chemical reactions allows for the introduction of specific functional groups required for drug development. It can be used in the creation of bioactive molecules, intermediates, and prodrugs, contributing to the advancement of medicinal chemistry.
- Agrochemicals: The compound finds use in the synthesis of agrochemicals, including pesticides and herbicides. Its unique structure and reactivity enable the creation of compounds that exhibit targeted action against pests, weeds, and pathogens. This contributes to the development of sustainable agricultural practices by reducing the environmental impact of chemical interventions.
- Materials Science: N-(2-Chloroethyl)benzenesulfonamide can be employed in the synthesis of functional materials for various applications. It can serve as a precursor in the creation of polymers, coatings, and specialty chemicals. Its ability to undergo polymerization and crosslinking reactions makes it valuable in designing materials with tailored properties, such as adhesion, corrosion resistance, and thermal stability.
- Chemical Research: Researchers may use N-(2-Chloroethyl)benzenesulfonamide as a starting material for exploring new chemical reactions and developing innovative synthetic methodologies. Its unique combination of functional groups can lead to the discovery of novel transformations and the synthesis of complex molecules.
Additional information
Pack Size | 50mg |
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