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1-chloro-2-methylprop-1-ene 2-methylprop-1-ene
[CAS# 68442-33-1]

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Identification
Classification Chemical reagent >> Organic reagent >> Olefins (cyclic and non-cyclic)
Name 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene
Molecular Structure CAS # 68442-33-1, 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene
Molecular Formula C8H15Cl
Molecular Weight 146.66
CAS Registry Number 68442-33-1
EC Number 614-508-0
SMILES CC(=C)C.CC(=CCl)C
up Discovory and Applicatios
1-Chloro-2-methylprop-1-ene 2-methylprop-1-ene, often known in the chemical literature by its IUPAC name as 2-Chloro-2-methylprop-1-ene or by its common name, is a compound of significant interest in the field of organic chemistry and polymer science. This substance is notable for its unique structure and reactivity, which open up a range of applications in both industrial and research settings.

The discovery of 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene can be traced back to research aimed at developing new monomers with tailored properties for polymerization. This compound is an example of a functionalized alkene with a chlorine atom and a double bond, which introduces reactive sites that can be used in various chemical transformations. The development of this compound involved the synthesis of its chlorinated derivative, where the chlorine atom is strategically placed to affect the reactivity and polymerization behavior of the molecule.

The synthesis of 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene typically involves the chlorination of 2-methylprop-1-ene, which introduces a chlorine atom into the molecule. This process can be carried out under controlled conditions to ensure the selective chlorination at the desired position. The resulting compound exhibits unique properties due to the presence of both the chlorine atom and the double bond, making it a valuable monomer for various applications.

One of the primary applications of 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene is in the field of polymer chemistry. The compound's reactivity allows it to undergo polymerization to form polymers with tailored properties. The presence of the chlorine atom in the structure introduces functionality that can be used to create polymers with specific characteristics, such as improved solubility, stability, or reactivity. These polymers find applications in a range of industries, including plastics, coatings, and adhesives.

In the plastics industry, the use of 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene as a monomer allows for the production of specialty polymers with enhanced properties. The chlorine atom in the molecule can influence the polymer's performance, such as its thermal stability and chemical resistance. This makes the resulting polymers suitable for use in demanding applications, including automotive components, electrical insulation, and consumer goods.

The compound is also used in the development of advanced coatings and adhesives. The ability to incorporate 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene into coating formulations allows for the creation of coatings with improved adhesion, durability, and resistance to environmental factors. These coatings are valuable in protecting various substrates, including metals, plastics, and textiles, from corrosion, wear, and other forms of degradation.

In addition to its industrial applications, 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene is of interest in research settings for its potential in developing new materials and chemical processes. The compound's reactivity and unique structure make it a useful tool for studying reaction mechanisms, polymerization processes, and the properties of functionalized polymers.

Overall, 1-chloro-2-methylprop-1-ene 2-methylprop-1-ene is a versatile compound with significant applications in polymer chemistry and materials science. Its discovery and development have led to the creation of specialty polymers and materials with enhanced properties, benefiting various industries and advancing research in chemical synthesis and materials science.
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