1,3-Dichloro-1,1,2,2,3,3-hexafluoropropane (CAS 662-01-1): A Crucial Fluorinated Intermediate for Advanced Synthesis

In the expansive realm of specialized chemical compounds, 1,3-dichloro-1,1,2,2,3,3-hexafluoropropane, identified by its CAS Registry Number 662-01-1, stands out as a highly versatile and significant fluorinated intermediate. This compound, also known by synonyms such as 1,3-dichlorohexafluoropropane or HCFC 216ca, is a critical building block for various advanced chemical processes, especially where precise fluorination is required. Its unique molecular structure, featuring both chlorine and fluorine atoms along a propane backbone, endows it with distinct chemical properties that make it indispensable in modern organic synthesis.

The chemical profile of 1,3-dichloro-1,1,2,2,3,3-hexafluoropropane is characterized by its molecular formula C3Cl2F6 and a molecular weight of 220.93 g/mol. Key physical properties further highlight its utility: it has a boiling point ranging from 35 to 36°C, a density of approximately 1.573 g/cm³ at 20°C, and a refractive index of 1.303. These specific parameters contribute to its handling characteristics and reactivity, making it a reliable reactant in controlled synthetic environments. The compound's high purity, typically at 95% minimum, ensures consistency and efficiency in downstream applications, which is paramount for sensitive chemical reactions.

The applications of 1,3-dichloro-1,1,2,2,3,3-hexafluoropropane are diverse, primarily centering on its role as a key intermediate in the synthesis of complex organic molecules. Its presence of multiple fluorine atoms and two reactive chlorine atoms makes it an excellent precursor for introducing fluoroalkyl groups into various compounds. This is particularly valuable in the pharmaceutical industry for creating new drug candidates with enhanced metabolic stability or bioavailability, and in the agrochemical sector for developing active ingredients with improved efficacy and environmental profiles. Beyond these, it finds use in the development of specialized materials, contributing to the creation of polymers and other advanced substances with tailored properties. While historically associated with the broader class of hydrochlorofluorocarbons (HCFCs), its modern relevance is predominantly as a precise synthetic reagent, allowing chemists to construct intricate molecular architectures with high specificity.

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