153042-33-2

Usage

Uses

Used in Pesticide Industry:
Tert-butyl (5-chloro-2-iodophenyl)carbamate is used as an active ingredient in pesticides for its ability to inhibit the activity of certain enzymes in pests, thereby controlling their populations and protecting crops.
Used in Insecticide Industry:
In the insecticide sector, tert-butyl (5-chloro-2-iodophenyl)carbamate is employed as an effective agent against insects, leveraging its enzyme-inhibiting properties to disrupt their physiological processes and reduce infestations.
Used in Agricultural Applications:
Tert-butyl (5-chloro-2-iodophenyl)carbamate is used as a crop protectant, ensuring the health and yield of agricultural products by mitigating the impact of pests through its pesticidal action.
Synthesis:
Tert-butyl (5-chloro-2-iodophenyl)carbamate is typically synthesized through a series of chemical reactions, starting with the reaction of tert-butyl isocyanate with 5-chloro-2-iodophenol, highlighting its importance in the field of organic chemistry and chemical engineering.

Upstream product

• 24424-99-5 di-tert-butyl dicarbonate 
• 6828-35-9 5-chloro-2-iodoaniline 
• 89-63-4 4-Chloro-2-nitroaniline 
• 5446-05-9 4-chloro-2-nitroiodobenzene 

Downstream Products

• 153042-35-4 (S)-4-[2-(2-Amino-4-chloro-phenyl)-2-oxo-ethyl]-5-oxo-oxazolidine-3-carboxylic acid benzyl ester 
• 175777-22-7 L-4-chlorokynurenine 
• 1448535-64-5 tert-butyl 5-chloro-2-iodophenyl(propionyl)carbamate 
• 1448535-73-6 (E)-tert-butyl 5-chloro-2-iodophenyl(prop-1-enyl)carbamate 
• 1609264-31-4 tert-butyl (5-chloro-2-iodophenyl)(2-methylallyl)carbamate 

Relevant academic research and scientific papers

Highly Enantioselective Cross-Electrophile Aryl-Alkenylation of Unactivated Alkenes

Enantioselective cross-electrophile reactions remain a challenging subject in metal catalysis, and with respect to data, studies have mainly focused on stereoconvergent reactions of racemic alkyl electrophiles. Here, we report an enantioselective cross-el

Highly Enantioselective Cross-Electrophile Aryl-Alkenylation of Unactivated Alkenes

Enantioselective cross-electrophile reactions remain a challenging subject in metal catalysis, and with respect to data, studies have mainly focused on stereoconvergent reactions of racemic alkyl electrophiles. Here, we report an enantioselective cross-el

Diversely Substituted Quinolines via Rhodium-Catalyzed Alkyne Hydroacylation

The Rh-catalyzed hydroacylative union of aldehydes and o-alkynyl anilines leads to 2-aminophenyl enones, and onward to substituted quinolines. The mild reaction conditions employed in this chemistry result in a process that displays broad functional group

INHIBITORS OF CYTOMEGALOVIRUS

Compounds of Formula (I) wherein R1, R2, R3A, R3B, Y, Z1 and Z2 are defined herein, are useful for the treatment of cytomegalovirus disease and/or infection.

Microwave-assisted synthesis of 3-substituted indoles via intramolecular arene-alkene coupling of o-iodoanilino enamines

A generally applicable and high-yielding protocol for the synthesis of 3-substituted indole derivatives is described. Key features include microwave-assisted intramolecular arene-alkene coupling of o-iodoanilino enamines, and expedient synthesis of o-iodo