CAS 5673-07-4: Understanding 2,6-Dimethoxytoluene for Chemical Synthesis
For professionals engaged in chemical synthesis, a deep understanding of key intermediates like 2,6-Dimethoxytoluene (CAS 5673-07-4) is fundamental. This aromatic compound, characterized by its specific arrangement of methoxy groups, serves as a crucial component in the creation of more complex molecules across various industries, including pharmaceuticals and specialty chemicals.
The chemical identity of 2,6-Dimethoxytoluene is defined by its CAS number, 5673-07-4, and its molecular formula C9H12O2. It typically appears as a white to yellowish crystalline solid, with a melting point range of 39-41°C. This physical state and its solubility profile (insoluble in water but soluble in organic solvents) make it amenable to standard laboratory and industrial chemical processing techniques. Manufacturers often guarantee a high purity level, commonly 97% or above, which is essential for reliable reaction outcomes.
Researchers and procurement officers frequently search for terms like 'buy 2,6-dimethoxytoluene' or 'CAS 5673-07-4 synthesis intermediate'. As a prominent manufacturer and supplier of these vital chemical building blocks, we ensure consistent quality and availability. Our strategic location in China allows us to offer competitive 2,6-dimethoxytoluene price points, making it accessible for a broad range of synthetic applications. We cater to clients requiring bulk quantities for industrial production as well as smaller amounts for research and development purposes.
The utility of 2,6-Dimethoxytoluene as an organic synthesis building block lies in its versatile reactivity. The methoxy groups and the methyl substituent on the aromatic ring allow for targeted chemical modifications, enabling the construction of diverse molecular architectures. This makes it a preferred choice in multi-step synthesis projects where precise control over reaction pathways is critical.
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“This makes it a preferred choice in multi-step synthesis projects where precise control over reaction pathways is critical.”
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