CAS 33278-96-5
:2-(bromomethyl)-2-methyl-1,3-dioxolane
Description:
2-(Bromomethyl)-2-methyl-1,3-dioxolane is a chemical compound characterized by its unique structure, which includes a dioxolane ring and a bromomethyl group. This compound features a five-membered cyclic ether with two oxygen atoms and a bromine substituent, contributing to its reactivity and potential applications in organic synthesis. The presence of the bromomethyl group makes it a useful intermediate in various chemical reactions, particularly in nucleophilic substitution processes. The dioxolane ring enhances the compound's stability and solubility in organic solvents, making it suitable for use in diverse chemical environments. Additionally, the compound's molecular structure allows for potential applications in the synthesis of pharmaceuticals, agrochemicals, and other organic materials. Its reactivity can be influenced by factors such as temperature and the presence of other reagents, which can lead to a variety of derivatives. As with many brominated compounds, safety precautions should be taken due to the potential for toxicity and environmental impact.
Formula:C5H9BrO2
InChI:InChI=1/C5H9BrO2/c1-5(4-6)7-2-3-8-5/h2-4H2,1H3
SMILES:CC1(CBr)OCCO1
Synonyms:- 1,3-Dioxolane, 2-(bromomethyl)-2-methyl-
- 2-(Bromomethyl)-2-methyl-1,3-dioxolane
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Found 3 products.
2-(Bromomethyl)-2-methyl-1,3-dioxolane
CAS:2-(Bromomethyl)-2-methyl-1,3-dioxolanePurity:95%Molecular weight:181.03g/mol2-(Bromomethyl)-2-methyl-1,3-dioxolane
CAS:Controlled Product<p>Applications 2-(Bromomethyl)-2-methyl-1,3-dioxolane is derived from Acetone (A163800), which is a common organic building block in organic chemistry.<br>References Neubert, L., et al.: J. Am. Chem. Soc., 134, 12239 (2012); Zhai, J.J., et al.: J. Am. Soc. Mass. Spec., 20, 1366 (2009);<br></p>Formula:C5H9BrO2Color and Shape:NeatMolecular weight:181.028
