Description

2-(Bromomethyl)-2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolane (CAS No. 60207-89-8) is a highly specialized brominated dioxolane derivative with a molecular formula of C₁₃H₁₅BrCl₂O₂. This compound features a unique structural framework, combining a bromomethyl group, a 2,4-dichlorophenyl moiety, and a propyl-substituted 1,3-dioxolane ring, making it a valuable intermediate in synthetic organic chemistry and pharmaceutical research. With a purity grade suitable for laboratory and industrial applications, this chemical is rigorously tested to ensure consistency and reliability. It is ideal for use in nucleophilic substitution reactions, cross-coupling methodologies, and as a precursor in the synthesis of complex heterocyclic compounds. Proper handling under controlled conditions is recommended due to its reactive bromomethyl group.

Properties

• CAS Number: 60207-89-8
• Complexity: 280
• IUPAC Name: 2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolane
• InChI: InChI=1S/C13H15BrCl2O2/c1-2-3-10-7-17-13(8-14,18-10)11-5-4-9(15)6-12(11)16/h4-6,10H,2-3,7-8H2,1H3
• InChI Key: PJVTZAKVRVBCMJ-UHFFFAOYSA-N
• Exact Mass: 351.96325
• Molecular Formula: C13H15BrCl2O2
• Molecular Weight: 354.1
• SMILES: CCCC1COC(O1)(CBr)C2=C(C=C(C=C2)Cl)Cl
• Topological: 18.5
• Monoisotopic Mass: 351.96325
• Synonyms: 60207-89-8, 2-(Bromomethyl)-2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolane, EINECS 262-103-9, DTXSID10866795, EC 262-103-9, DTXCID60815036, 262-103-9, 1,3-Dioxolane, 2-(bromomethyl)-2-(2,4-dichlorophenyl)-4-propyl-, Destriazolyl Bromo Propiconazole, PJVTZAKVRVBCMJ-UHFFFAOYSA-N, starbld0047155, SCHEMBL10785905, KCA20789, AKOS028108330, DA-04520, NS00004225, 2-bromomethyl-2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolane

Application

2-(Bromomethyl)-2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolane is primarily utilized as a key synthetic intermediate in the preparation of biologically active molecules, particularly in pharmaceutical and agrochemical research. Its reactive bromomethyl group enables facile functionalization, making it suitable for constructing diverse molecular architectures. Researchers employ this compound in cross-coupling reactions and as a building block for heterocyclic systems. It may also serve as a precursor in the development of antifungal or antimicrobial agents due to its dichlorophenyl moiety. Strict adherence to safety protocols is advised during use.

Safety and Hazards

GHS Hazard Statements

• H317 (96.6%): May cause an allergic skin reaction [Warning Sensitization, Skin]
• H411 (96.6%): Toxic to aquatic life with long lasting effects [Hazardous to the aquatic environment, long-term hazard]

Precautionary Statements

• P261, P272, P273, P280, P302+P352, P321, P333+P317, P362+P364, P391, and P501

Hazard Classes and Categories

• Skin Sens. 1 (96.6%)
• Aquatic Chronic 2 (96.6%)

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