863870-80-8

Usage

Uses

Used in Agricultural Applications:
2,3-Dibromophenyl N,N-diethylcarbamate is used as an insecticide and acaricide for controlling pests such as mites, aphids, and leafhoppers on crops. Its application helps protect agricultural produce from damage caused by these pests, ensuring a healthy and productive yield.
Used in Stored Product Protection:
2,3-DIBROMOPHENYL N,N-DIETHYLCARBAMATE is also used as a protective measure for stored products, where it helps to prevent infestations by insects and mites that could lead to spoilage and economic loss.
Used in Livestock Management:
In the livestock industry, 2,3-Dibromophenyl N,N-diethylcarbamate is used to control pests that may infest animals, thus maintaining the health and well-being of the livestock and reducing the risk of disease transmission.
It is crucial to handle 2,3-Dibromophenyl N,N-diethylcarbamate with care, as it can pose risks to humans and non-target organisms if not used according to safety guidelines. Adherence to strict safety measures is essential when applying this chemical to minimize potential harm.

Upstream product

• 863870-72-8 O-3-bromophenyl N,N-diethylcarbamate 
• 591-20-8 3-Bromophenol 
• 88-10-8 N,N-diethylcarbamyl chloride 

Downstream Products

• 1287791-69-8 2-(2,3-dibromophenoxy)-2-methylpropanamide 
• 1287791-78-9 N-(2,3-dibromophenyl)-2-hydroxy-2-methylpropanamide 
• 608-22-0 3-amino-1,2-dibromobenzene 
• 1385058-19-4 C₁₈H₁₂O₂ 
• 1385058-24-1 C₁₈H₁₂O₄S 
• 57383-80-9 2,3-dibromophenol 

Relevant academic research and scientific papers

Regioselectivity of Diels-Alder reactions between 6,7-dehydrobenzofuran and 2-substituted furans

We describe the first report of the generation of 6,7-dehydrobenzofuran(6, 7-benzofuranyne) from 6,7-dihalobenzofurans via metal-halogen exchange and elimination, in a manner similar to our previous work with 6,7-indole arynes. This benzofuranyne undergoe

Approaches to the synthesis of 2,3-dihaloanilines. Useful precursors of 4-functionalized-1 H-indoles

2,3-Dihaloanilines have been proved as useful starting materials for synthesizing 4-halo-1H-indoles. Subsequent or in situ functionalization of the prepared haloindoles allows the access to a wide variety of 2,4- or 2,3,4-regioselectively functionalized indoles in good overall yields. As no efficient synthetic routes to 2,3-dihaloanilines have been described in the literature, different approaches to the preparation of these 1,2,3-functionalized aromatic precursors are now presented. The most general one involves a Smiles rearrangement from the corresponding 2,3-dihalophenols and allows the preparation of 2,3-dihaloanilides in a straightforward and synthetically useful manner.

A new and efficient synthesis of 4-functionalized benzo[6]furans from 2,3-dihalophenols

Tandem Sonogashira coupling/5-endo-dig cyclization reactions on 2,3-dihalophenols suppose a straightforward entry to 4-halobenzo[b]furans, which can be easily transformed into 4-functionalized benzo[b]furans, that are difficult to synthesize by other proc