3389-57-9

Usage

Uses

Used in Pharmaceutical Industry:
4-TETRAHYDRO-1H-PYRROL-1-YLPENT-3-EN-2-ONE is used as a chemical precursor for the synthesis of various pharmaceuticals. Its unique structure allows it to be a key component in the development of new drugs, contributing to the advancement of medicinal chemistry.
Used in Agrochemical Industry:
In the agrochemical sector, 4-TETRAHYDRO-1H-PYRROL-1-YLPENT-3-EN-2-ONE serves as a precursor in the production of agrochemical products. Its role in creating effective and safe pesticides and other agricultural chemicals is crucial for enhancing crop protection and yield.
Used in Polymer Production:
4-TETRAHYDRO-1H-PYRROL-1-YLPENT-3-EN-2-ONE is utilized as a monomer in the synthesis of polymers. Its incorporation into polymer chains can impart specific properties, such as improved strength or flexibility, making it an essential component in material science.
Used in Specialty Chemicals:
4-TETRAHYDRO-1H-PYRROL-1-YLPENT-3-EN-2-ONE is also used in the creation of specialty chemicals, where its unique chemical properties can be tailored to meet specific industrial needs. Its versatility in organic synthesis makes it a valuable asset in the development of customized chemical products.

InChI:InChI=1/C9H15NO/c1-8(7-9(2)11)10-5-3-4-6-10/h7H,3-6H2,1-2H3/b8-7-

Upstream product

• 123-75-1 pyrrolidine 
• 123-54-6 acetylacetone 
• 85143-85-7 4-(1-imidazolyl)-3-penten-2-one 
• 85143-87-9 1-(4-oxo-2-penten-2-yl)-3-methylimidazolium iodide 

Downstream Products

• 115018-15-0 4-<5-Oxo-1,3-diphenyl-2-(1-pyrrolidinoethyliden)-3-hexenyliden>morpholinium-trifluormethansulfonat 
• 75476-16-3 (2E,4E)-4-Methyl-2,3-diphenyl-1-pyrrolidin-1-yl-hepta-2,4-diene-1,6-dione 
• 501-65-5 diphenyl acetylene 
• 115018-22-9 4-Methyl-2-phenyl-6-pyrrolidinobenzophenon 
• 769-28-8 3-Cyano-4,6-dimethyl-2(1H)-pyridon 
• 116986-88-0 4,6-dimethyl-2-(1-pyrrolidinyl)acetophenone 
• 682345-11-5 ethyl 3-acetyl-6-hydroxy-4-pyrrolidin-1-yl-6-(trifluoromethyl)cyclohexa-1,3-diene-1-carboxylate 
• 1346229-25-1 1-(2-amino-5-(4-chlorobenzoyl)-4-methyl-1H-pyrrol-3-yl)ethanone 
• 1346229-26-2 C₁₅H₁₆N₂O₂ 
• 1346229-27-3 C₁₅H₁₆N₂O₃ 
• 1346229-29-5 C₁₄H₁₄N₂O₂ 
• 1346229-30-8 C₁₄H₁₃BrN₂O₂ 
• 1346229-31-9 C₁₄H₁₂Cl₂N₂O₂ 
• 1346229-32-0 C₁₆H₁₇N₃O₃ 

Relevant academic research and scientific papers

A multicomponent reaction as a versatile tool for the synthesis of spirooxindoles using N-alkylisatins; efficient catalysis by ZnO nanoparticles

An efficient and green protocol for the synthesis of functionalised spirooxindole derivatives is described. This involves the reaction of in situ-generated keto-enaminones with N-alkylisatins in the presence of isothiocyanates.

Reactivities of 3-(1-Azolyl)-2-alken-1-ones and the Related Compounds With Pyrrolidine

From the rate constants of the reaction with pyrrolidine, the reactivities of 3-(1-azolyl)-2-alken-1-ones with nucleophiles were evaluated to be rather high.Especially the reactivities of the quarternary salts of 3-(1-imidazolyl)-2-alken-1-ones were nearly equal to those of 3-chloro-2-alken-1-ones.In conclusion, 3-(1-imidazolyl)-2-alken-1-ones satisfied the practical requirements for the starting materials of the synthesis of 3-hetero-substituted 2-alken-1-ones.