54580-23-3

Usage

Uses

Used in Polymer Industry:
2,4-Hexadiene, 2,5-dimethyl-3,4-bis(1-methylethyl)is used as a monomer in the polymer industry for the production of various polymers. Its presence in the polymerization process contributes to the formation of polymers with specific properties, such as enhanced strength, flexibility, or chemical resistance, depending on the desired application.
Used in Fragrance Industry:
In the fragrance industry, 2,4-Hexadiene, 2,5-dimethyl-3,4-bis(1-methylethyl)is used as a component in the synthesis of various fragrances. Its unique chemical structure allows it to contribute to the creation of distinct scents and aromas, enhancing the sensory experience of the final product.
Used in Pharmaceutical Industry:
2,4-Hexadiene, 2,5-dimethyl-3,4-bis(1-methylethyl)is also utilized in the pharmaceutical industry for the synthesis of various organic compounds. Its versatile chemical properties make it a valuable intermediate in the production of pharmaceuticals, potentially contributing to the development of new drugs or improving the synthesis process of existing ones.
Safety Considerations:
Due to its flammable nature, 2,4-Hexadiene, 2,5-dimethyl-3,4-bis(1-methylethyl)should be handled with care in a well-ventilated area to minimize the risk of fire or explosion. Proper safety measures, such as the use of protective equipment and adherence to safety protocols, are essential when working with 2,4-Hexadiene, 2,5-dimethyl-3,4-bis(1-methylethyl)-.

InChI:InChI=1/C14H26/c1-9(2)13(10(3)4)14(11(5)6)12(7)8/h9,11H,1-8H3

Upstream product

• 34106-07-5 2,5-dimethyl-2,5-diacetoxy-3-hexyne 
• 920-39-8 isopropylmagnesium bromide 
• 54580-22-2 4-isopropyl-3-isopropylidene-2,5-dimethylhexa-1,4-diene 
• 69856-67-3 3,3,3',3',5,5,5',5'-octamethyl-3,3',5,5'-tetrahydro-4,4'-bi(4H-pyrazolylidene) 
• 58721-02-1 2,2,4,4-tetramethylthietan-3-one 1,1-dioxide 
• 1000-87-9 2,4-dimethyl-2,3-pentadiene 
• 94526-05-3 2,2,2',2',4,4,4',4'-octamethyl-3,3'-bithietanylidene 1,1,1',1'-tetraoxide 
• 94526-03-1 2,2,2'',2'',4,4,4'',4''-octamethyl-2',5'-dihydro<1,3,4>thiadiazole-2',5'-dispiro-3,3''-bis(thietane) 1,1,1'',1''-tetraoxide 
• 94526-04-2 2,2,2'',2'',4,4,4'',4''-octamethylthiirane-2',3'-dispiro-3,3''-bis(thietane) 1,1,1'',1''-tetraoxide 
• 94526-02-0 3-diazo-2,2,4,4-tetramethylthietane 1,1-dioxide 
• 94525-98-1 (2,2,4,4-Tetramethyl-1,1-dioxo-1λ⁶-thietan-3-ylidene)-hydrazine 
• 1133-23-9 1,2-di-isopropylidene-3,3,4,4-tetramethylcyclobutane 

Relevant academic research and scientific papers

Sterically Hindered Double Bond Systems, 2. - On the Preparation of Highly Substituted 1,3-Dienes

Highly alkylated 1,3-dienes may be prepared by treatment of 2-butyne-1,4-diol derivatives with organocuprates in good yield.Thus, the 2,3-dialkylated butadienes 6a-d are obtained by treating the diacetate 4 with two equivalents of the cuprates prepared fr

Preparation, Pyrolysis, and Photolysis of Three Sterically Crowded Alkenes, 3,3,3',3',5,5,5',5'-Octamethyl-3,3',5,5'-tetrahydro-4,4'-bi(4H-pyrazolylidene) 2,2,4,4-Tetramethyl-3-(3,3,5,5-tetramethyl-3,5-dihydro-4H-pyrazol-4-ylidene)-thietane 1,1-Dioxide and 2,2,2',2',4,4,4',4'-Octameth...

Photolysis and pyrolysis of the title compounds involve a stepwise elimination of nitrogen and/or sulphur dioxide and reactions which can be interpreted in terms of a series of trimethylenemethane (TMM) biradical intermediates.However, the photosensitised photolysis of the bi(pyrazolylidene) (11) give products indicative of an elimination of both nitrogens and the generation of a tetramethylene-ethane (TME) biradical intermediate.New synthesis of a number of highly sterically crowded alkenes including 2,2,4,4-tetramethyl-3-(3,3,5,5-tetramethyl-3,4-dihydro-4H-pyrazol-4-ylidene)thietane 1,1-dioxide (12) and 2,2,2',2',4,4,4',4'-octamethyl-3,3'-bithietanylidene 1,1,1',1'-tetraoxide (13), are described.Flash vacuum pyrolysis (f.v.p) of 3,3,3',3',5,5,5',5'-octamethyl-3,3'-5,5'-tetrahydro-4,4'-bi(4H-pyrazolylidene) (11) at 400 deg C gives 3,3,5,5-tetramethyl-4-(2,2,3,3-tetramethylcyclopropylidene)-3,5-dihydro-4H-pyrazole (21), at ca. 400 deg C 1-isopropylidene-2,2,4,4,5,5-hexamethylspiropentane (22), and at ca. 580 deg C a ca. 5:1 mixture of 4-isopropyl-3-isopropylidene-2,5-dimethylhexa-1,4-diene (23) and 2-(2,3-dimethylbut-1-en-3-yl)-1-isopropyl-3,3-dimethylcyclopropene (27).Above 700 deg C a complex mixture of aromatic products and low molecular weight hydrocarbons is produced which includes ethane, ethylene, propene, isobutane, and isobutene, p-xylene, o-cumene and probably m-cumene, and 2,5-dimethylisopropylbenzene.F.v.p. of the dihydropyrazole sulphone (12) gives initially 2,2,4,4-tetramethyl-3-(2,2,3,3,-tetramethylcyclopropylidene)thietane 1,1-dioxide (41) and at higher temperatures similar mixtures to those obtained from the bipyrazolylidene (11).Similar results were also obtained for the f.v.p. of the bis-sulphone (13).Photolysis of the bipyrazolylidene (11) gave initially the dihydropyrazole (21) and then a 48:52 mixture of the spiro compound (22) and 2,2,2',2',3,3,3',3'-octamethylbicyclopropylidene (42).Photolysis of the dihydropyrazole sulphone (12) gave 2,2,4,4-tetramethyl-3-(2,2,3,3-tetramethylcyclopropylidene)thietane 1,1-dioxide (41).Benzophenone-sensitised photolysis of the bipyrazolylidene (11) gave 1,2-di-isopropylidene-3,3,4,4-tetramethylcyclobutane (32).