756-02-5

Usage

Uses

Used in Polymer and Resin Production:
2,3,3-Trimethyl-1,4-pentadiene is used as a monomer in the production of polymers and resins. Its high reactivity makes it a valuable component in the synthesis of various types of plastics and resinous materials, contributing to their structural properties and performance.
Used in Solvent Applications:
As a solvent, 2,3,3-Trimethyl-1,4-pentadiene is utilized in various industrial processes. Its ability to dissolve a wide range of substances makes it a versatile component in the formulation of solutions for different applications, such as in chemical reactions or cleaning processes.
Used in Adhesive, Sealant, and Coating Manufacture:
2,3,3-Trimethyl-1,4-pentadiene is incorporated into the production of adhesives, sealants, and coatings. Its presence in these formulations can enhance their adhesive properties, durability, and resistance to environmental factors, making them suitable for various applications in construction, automotive, and other industries.

InChI:InChI=1/C8H14/c1-6-8(4,5)7(2)3/h6H,1-2H2,3-5H3

Upstream product

• 102369-82-4 2,2,3,3-tetramethyl-tetrahydro-furan 
• 1195-83-1 4-tert-butyl-4-methyl-[1,3]dioxane 
• 563-79-1 2,3-Dimethyl-2-butene 
• 74-86-2 acetylene 
• 54376-39-5 1,1,2,2-Tetramethyl-3-methylenecyclopropane 
• 135312-71-9 5-bromo-4-ethoxy-2,3,3-trimethyl-1-pentene 
• 58544-20-0 ethyl 2,2-dimethyl-3-butenoate 
• 292638-85-8 acrylic acid methyl ester 
• 36934-19-7 2,3,3-trimethyl-4-penten-2-ol 

Downstream Products

• 40441-35-8 3,4,4-trimethylcyclohexen-1-one 
• 117019-50-8 trans-2,3,3,4-Tetramethylcyclopentanon 
• 117019-51-9 cis-2,3,3,4-Tetramethylcyclopentanon 

Relevant academic research and scientific papers

A Versatile Synthesis of 1,4-Dienes: Use of Vinyl Ethers as Vinyl Cation Equivalents

The α,β-dibromo ethers 2, in situ generated from the vinyl ethers 1 and bromine, react with the allylsilanes 3 in the presence of ZnCl2 to give the β-bromo ethers 4.Treatment of 4 with Na in diethyl ether yields 1,4-dienes 5 in 62-79percent overall yield.Key Words: Enol ether / Allylsilane / Bromo ether / 1,4-Diene / Alkoxyalkylation

Regio- and Stereoselectivity of the Hydrocarbonylating Cyclization of 1,4-Dienes with Carbon Monoxide: Synthesis of (+/-)-(α)-Cuparenone

Directed towards the synthesis of the cuparene skeleton the hydrocarbonylating cyclization of 1,4-dienes 16, 27 to form cyclopentanones 17, 28 was tested for its regio- and stereoselectivity as well as the toleration of aryl groups in this cyclization met

Reactions of Methylenecyclopropanes, VII. Nickel(0)-catalysed Cycloadditions of Methylenecyclopropanes with Alkyl Acrylates

Cycloaddition reactions of methylenecyclopropane (1) and of the ring-methylated methylenecyclopropanes 5, 9, and 12 with alkyl acrylates are performed at nickel(0) catalysts, such as bis(1,5-cyclooctadiene)nickel under mild conditions (0 - 50 deg C).Depending on the degree of methylation of the three-membered ring, 1 and 5 give only alkyl 3-methylenecyclopentanecarboxylates (4 and 6), whereas 9 leads to a mixture of the methylenecyclopentane derivative 10 and the alkyl spirohexanecarboxylate 11, and 12 react to form only the spirohexane derivative 13.With 12 isomerisation to 2,3,3-trimethyl-1,4-pentadiene (15) also takes place.In the case of 9 the ratio of methylenecyclopentane to spirohexanecarboxylate can be influenced by the size of alkyl groups. - In the Ni0-catalysed reactions of 1 with substituted acrylates (methyl crotonate or diethyl maleate) codimerisation to 16 and 17 competes with cyclodimerisation to 2 and 3.