Description
Methyl 2-(chloromethyl)acrylate (CAS No. 922-15-6) is a highly versatile and reactive ester monomer with the molecular formula C5H7ClO2. This compound, also known by its IUPAC name methyl 2-(chloromethyl)prop-2-enoate, is a clear to pale yellow liquid with a characteristic acrid odor. It is widely utilized in polymer chemistry and organic synthesis due to its bifunctional reactivity, featuring both an acrylate group and a chloromethyl group. The chloromethyl moiety allows for further functionalization, making it a valuable intermediate in the production of specialty polymers, coatings, and adhesives. This product is rigorously tested for purity and stability, ensuring optimal performance in research and industrial applications. Store in a cool, dry place under inert atmosphere to maintain its integrity.
Properties
- CAS Number: 922-15-6
- Complexity: 109
- IUPAC Name: methyl 2-(chloromethyl)prop-2-enoate
- InChI: InChI=1S/C5H7ClO2/c1-4(3-6)5(7)8-2/h1,3H2,2H3
- InChI Key: NYMDTEIPYQNXIL-UHFFFAOYSA-N
- Exact Mass: 134.0134572
- Molecular Formula: C5H7ClO2
- Molecular Weight: 134.56
- SMILES: COC(=O)C(=C)CCl
- Topological: 26.3
- Monoisotopic Mass: 134.0134572
- Synonyms: METHYL 2-(CHLOROMETHYL)ACRYLATE, 922-15-6, methyl 2-(chloromethyl)prop-2-enoate, methyl2-(chloromethyl)acrylate, MFCD11617809, (?)-2-Hydroxyisopinocampheol, SCHEMBL882348, DTXSID60498661, AKOS006317182, Methyl 2-(chloromethyl)acrylate, 95%, 2-(Chloromethyl)acrylic acid methyl ester, AS-33344, FM154677, DB-079272, CS-0208489, EN300-7390197, [1R-(1?,2?,3?,5?)]-2,6,6-Trimethylbicyclo[3.1.1]heptane-2,3-diol
Application
Methyl 2-(chloromethyl)acrylate is primarily used as a reactive monomer in the synthesis of functionalized polymers and copolymers. Its dual reactivity enables the creation of cross-linked networks, enhancing mechanical and thermal properties in materials. This compound is also employed in the preparation of ion-exchange resins and specialty coatings with tailored surface characteristics. Researchers value it for its role in post-polymerization modifications, allowing the introduction of additional functional groups. Its applications extend to the development of biomedical materials and advanced adhesives.
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