10047-90-2

Usage

Uses

Used in Agricultural and Horticultural Industries:
Propan-2-yl N-methylcarbamate is used as a carbamate insecticide for controlling a wide range of pests in agricultural and horticultural crops. It is effective in managing pests that can cause significant damage to crops, thereby protecting the yield and quality of the produce.
Used in Pest Management:
Propan-2-yl N-methylcarbamate serves as a crucial tool in pest management, helping to reduce the impact of pests on crops and ensuring a stable food supply. Its ability to target and eliminate pests makes it a valuable component in integrated pest management strategies.
Used in Regulatory Frameworks:
Due to its toxicity to humans and non-target organisms, propan-2-yl N-methylcarbamate is used as a subject of regulatory frameworks to ensure its safe and responsible application. These regulations aim to minimize the potential harm to the environment and human health by setting guidelines for its use, disposal, and monitoring of residues in food products.

InChI:InChI=1/C5H11NO2/c1-4(2)8-5(7)6-3/h4H,1-3H3,(H,6,7)

Upstream product

• 108-23-6 isopropyl chloroformate 
• 74-89-5 methylamine 
• 22013-97-4 N-methyl-thiocarbamic acid S-methyl ester 
• 67-63-0 isopropyl alcohol 
• 82998-18-3 isopropyl 1H-imidazole-1-carboxylate 

Downstream Products

• 1129-48-2 N-methyl-carbamic acid 4-tolyl ester 
• 3938-29-2 4-methoxyphenyl N-methylcarbamate 
• 1943-79-9 N-Methyl-O-phenylcarbamat 
• 2231-31-4 dimethyl (isopropoxycarbonyl)methylphosphoramidate 
• 1128-78-5 2-methylphenyl N-methylcarbamate 
• 3942-54-9 2-chlorophenyl N-methylcarbamate 

Relevant academic research and scientific papers

Transesterification of alkyl carbamate to aryl carbamate : Effect of varying the alkyl group

Phosphorus oxychloride mediated transesterification of four alkyl N-methylcarbamates to several aryl N-methylcarbamates has been studied. Best yields are obtained from benzyl N-methylcarbamate.

Photochemistry of N-acetyl-, N-trifluoroacetyl-, N- mesyl-, and N-tosyldibenzothiophene sulfilimines

(Chemical Equation Presented) Time-resolved infrared (TRIR) spectroscopy, product studies, and computational methods were applied to the photolysis of sulfilimines derived from dibenzothiophene that were expected to release acetylnitrene, trifluoroacetylnitrene, mesylnitrene, and tosylnitrene. All three methods provided results for acetylnitrene consistent with literature precedent and analogous experiments with the benzoylnitrene precursor, i.e., that the ground-state multiplicity is singlet. In contrast, product studies clearly indicate triplet reactivity for trifluoroacetylnitrene, though TRIR experiments were more ambiguous. Product studies suggest that these sulfilimines are superior sources for sulfonylnitrenes, which have triplet grounds states, to the corresponding azides, and computational studies shed light on the electronic structure of the nitrenes.