153042-33-2

Basic information

• Product Name: tert-butyl (5-chloro-2-iodophenyl)carbamate
• Synonyms: tert-butyl (5-chloro-2-iodophenyl)carbamate
• CAS NO: 153042-33-2
• Molecular Weight: 353.587
• Mol File: 153042-33-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: tert-butyl (5-chloro-2-iodophenyl)carbamate(CAS DataBase Reference)
• NIST Chemistry Reference: tert-butyl (5-chloro-2-iodophenyl)carbamate(153042-33-2)
• EPA Substance Registry System: tert-butyl (5-chloro-2-iodophenyl)carbamate(153042-33-2)

Safety Data

• Hazardous Substances Data: 153042-33-2(Hazardous Substances Data)

Usage

General Description

Tert-butyl (5-chloro-2-iodophenyl)carbamate is a chemical compound that is a carbamate derivative with a tert-butyl group attached to the carbamate nitrogen atom and a chlorine and iodine atom attached to the phenyl ring. It is commonly used as a pesticide or insecticide due to its ability to inhibit the activity of certain enzymes in pests. tert-butyl (5-chloro-2-iodophenyl)carbamate is also known for its high stability and low toxicity to humans and the environment. It is typically synthesized through a series of steps involving the reaction of tert-butyl isocyanate with 5-chloro-2-iodophenol. Overall, tert-butyl (5-chloro-2-iodophenyl)carbamate is an important chemical with various applications in the field of agriculture and pest control.

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 articles and documents

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

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