4-Chloromethyl-5-methyl-1,3-dioxol-2-one TCI C1882

Chemical Identity

CAS No.: 80841-78-7
PubChem: CID 9855518·SID 87570450
Formula: C5H5ClO3
Molecular weight: 148.54 g/mol
Purity: >94.0%(GC)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: 4-(chloromethyl)-5-methyl-1,3-dioxol-2-one
SMILES: CC1=C(OC(=O)O1)CCl
InChIKey: QCLFSYYUWPUWQR-UHFFFAOYSA-N
MDL: MDL07787494

Rp 1.087.800,00

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Berat 5g 25g

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4-Chloromethyl-5-methyl-1,3-dioxol-2-one is a chemical compound widely used in organic synthesis as a building block for complex molecule development. Its unique structure, containing a chloromethyl group and a cyclic framework, makes it highly reactive in various chemical reactions. This compound is commonly applied in pharmaceutical research, material science, and industrial chemistry. Its stability under controlled conditions and reactivity in substitution and addition reactions make it a valuable tool for researchers in Indonesia. The availability of this compound in local markets supports scientific innovation and academic research in the country.

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Makosza et al. (2003). Chloromethyl Methyl Sulfone by Oxidation of Chloromethyl Methyl Sulfide.. ChemInform doi:10.1002/chin.200344059
Makosza et al. (2003). CHLOROMETHYL METHYL SULFONE BY OXIDATION OF CHLOROMETHYL METHYL SULFIDE. Organic Preparations and Procedures International doi:10.1080/00304940309355850
Guirgis et al. (1999). Conformational stability, vibrational spectra and ab initio calculations for chloromethyl methyl silane and chloromethyl methyl difluorosilane. Journal of Molecular Structure doi:10.1016/s0022-2860(98)00771-6

References were compiled automatically from Crossref and every DOI was verified to exist. AMI Scientific is not affiliated with the authors or the publishers.