886576-63-2

Usage

Uses

Used in Pharmaceutical Synthesis:
2,2-dimethylpent-4-enylcarbamic acid benzyl ester is used as a reagent in the synthesis of pharmaceuticals for its ability to participate in esterification reactions with various compounds. Its unique structure allows it to be a key component in the development of new drugs and therapeutic agents.
Used in Chemical Research:
In the field of chemistry, 2,2-dimethylpent-4-enylcarbamic acid benzyl ester is used as a research compound to study its properties and potential applications. Its unique structure and reactivity make it an interesting subject for chemical investigations and the development of new chemical processes.
Used in Pest Control (Agricultural Industry):
2,2-dimethylpent-4-enylcarbamic acid benzyl ester is used as an insecticide and acaricide in the agricultural industry due to its insecticidal and acaricidal properties. It helps in controlling pests and parasites that can damage crops and reduce agricultural productivity.

Upstream product

• 1186589-94-5 C₁₉H₂₇NO₅ 
• 1186589-91-2 C₁₈H₂₅NO₄ 
• 1186589-93-4 C₁₆H₂₃NO₃ 
• 2978-30-5 2,2-dimethylpent-4-enenitrile 
• 13139-17-8 N-(Benzyloxycarbonyloxy)succinimide 
• 73604-46-3 2,2-dimethyl-1-amino-pent-4-ene 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 1036403-92-5 C₁₆H₂₁NO₃ 
• 1124311-40-5 benzyl 4,4-dimethyl-2-((N-(phenylsulfonyl)phenylsulfonamido)methyl)-pyrrolidine-1-carboxylate 
• 1162740-07-9 benzyl 4,4-dimethyl-2-(4-methylbenzyl)-pyrrolidine-1-carboxylate 
• 1241922-20-2 benzyl 5-hydroxy-3,3-dimethyl-piperidine-1-carboxylate 
• 1241922-19-9 benzyl 5-methoxy-3,3-dimethylpiperidine-1-carboxylate 
• 1241922-03-1 benzyl 2-(methoxymethyl)-4,4-dimethylpyrrolidine-1-carboxylate 
• 1241922-05-3 benzyl 4,4-dimethyl-2-(n-propoxymethyl)-pyrrolidine-1-carboxylate 
• 1241922-21-3 benzyl 5-ethoxy-3,3-dimethyl-piperidine-1-carboxylate 
• 1241922-04-2 benzyl 2-(ethoxymethyl)-4,4-dimethylpyrrolidine-1-carboxylate 
• 1241922-08-6 benzyl 2-(acetoxymethyl)-4,4-dimethylpyrrolidine-1-carboxylate 
• 1241922-07-5 benzyl 2-(isopropoxymethyl)-4,4-dimethylpyrrolidine-1-carboxylate 
• 1241922-18-8 benzyl 2-(4-methoxybenzyloxymethyl)-4,4-dimethylpyrrolidine-1-carboxylate 
• 1241922-17-7 benzyl 2-benzyloxymethyl-4,4-dimethyl-pyrrolidine-1-carboxylate 
• 1241922-06-4 benzyl 4,4-dimethyl-2-(n-butoxymethyl)-pyrrolidine-1-carboxylate 

Relevant academic research and scientific papers

Asymmetric "clip-Cycle" Synthesis of Pyrrolidines and Spiropyrrolidines

The development of an asymmetric "clip-cycle"synthesis of 2,2- and 3,3-disubstituted pyrrolidines and spiropyrrolidines, which are increasingly important scaffolds in drug discovery programs, is reported. Cbz-protected bis-homoallylic amines were activate

Catalytic cyclization of alkenyl N,O-acetals by Fe(OTf)3

Fe(OTf)3, was found to be a good catalyst for the cyclization of alkenyl N,O-acetals to give various nitrogen-containing heterocycles in high yields. Copyright

Improved protocol for asymmetric, intramolecular heteroatom Michael addition using organocatalysis: Enantioselective syntheses of homoproline, pelletierine, and homopipecolic acid

(Chemical Equation Presented) An improved protocol for the construction of enantioenriched pyrrolidine, indoline, and piperidine rings using an organocatalyzed, intramolecular heteroatom Michael addition is described. Application to the enantioselective synthesis of homoproline, homopipecolic acid, and pelletierine has been accomplished.

Room temperature palladium-catalyzed intramolecular hydroamination of unactivated alkenes

A mild and facile Pd-catalyzed intramolecular hydroamination of unactivated alkenes is described. This reaction takes place at room temperature and is tolerant of synthetically useful acid-sensitive functional groups. The formation of hydroamination products rather than oxidative amination products is due to the use of a tridentate ligand on Pd which effectively inhibits β-hydride elimination. Copyright