3295-92-9

Usage

Uses

Used in Agriculture and Horticulture:
Propan-2-yl methyl(phenyl)carbamate is used as an insecticide and pesticide for controlling a wide range of pests, such as insects, mites, and nematodes, to protect crops and plants from damage. Its application helps maintain crop yield and quality by reducing the impact of pest infestations.
Used in Regulatory Frameworks:
Propan-2-yl methyl(phenyl)carbamate is used as a subject of regulatory considerations to ensure the safety of its application in agriculture and horticulture. Governments and regulatory bodies assess the potential human and environmental health hazards associated with carbaryl and establish guidelines and restrictions for its use to minimize risks.
Used in Research and Development:
Propan-2-yl methyl(phenyl)carbamate is utilized in research and development to study its effects on pests and to explore alternative pest control methods. Scientists investigate the mode of action, efficacy, and potential risks associated with carbaryl to develop safer and more effective pest management strategies.

Upstream product

• 122-42-9 carbamic acid, phenyl-, 1-methylethyl ester 
• 74-88-4 methyl iodide 
• 2388-10-5 lithium isopropoxide 
• 132431-15-3 2-(N-methylanilino)-2-phenylsulfanylacetonitrile 
• 36602-08-1 (N-methylanilino)acetonitrile 

Downstream Products

• 5327-53-7 4 hydroxy Probham 
• 122-42-9 carbamic acid, phenyl-, 1-methylethyl ester 
• 102992-50-7 [4-((2S,3R,4R,5S,6R)-3,4-Dihydroxy-6-hydroxymethyl-5-methoxy-tetrahydro-pyran-2-yloxy)-phenyl]-carbamic acid isopropyl ester 
• 99985-64-5 o-methylaminobenzoate d'isopropyle 

Relevant academic research and scientific papers

2-(N-Methylanilino)-2-phenylsulfanylacetonitrile, A Reagent Tested for Electrophilic, Nucleophilic, and Radical Reactions

2-(N-Methylanilino)-2-phenylsulfanylacetonitrile 1 has been readily prepared from 2-(N-methylanilino)acetonitrile and diphenyl disulfide.Alkylation of the anion of 1 with halogenoalkanes resulted in concurrent elimination of benzenethiol to give conjugated α-aminoalkenenitriles of 2E-configuration.Autoxidation of 1 in the presence of alkoxide ions afforded alkyl N-methyl-N-phenylcarbamates.Nucleophilic substitution of 1 with Grignard reagent or appropriate silyl compounds were promoted by CuI or Lewis acids to give varied α-amino nitriles.The 4-oxo-2-aminonitriles 9 obtained by condensation of 1 and titanium enolates can be considered as derivatives of 1,3-dicarbonyl compounds with the aldehyde group being activated to give an amino nitrile umpolung.When 1 was treated with tributylstannane, the corresponding amino nitrile α-radical was formed and the self-coupling product was isolated.

Reduction et photoreduction de derives de l'acide carbonique influence de l'hexamethylphosphorotriamide

Photoreduction and reduction of carbonic acid derivatives in HMPT have been compared.The highest yield of alkane was obtained from N,N-dimethylthiocarbamates either by the photochemical method or by reduction with a dissolved metal.Competitive reactions have been characterized: - during the photoreduction not only the alkane but products of a photo-Fries rearrangement and products of a homolytic cleavage were detected; - basic reactions can compete with the reduction of carbonic acid derivatives by sodium in HMPT.