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  XuxinCheng,XiaomingChen,PengyuanFan
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives Benzene and substituted derivatives
• Solvents and Organic Chemicals Organic Compounds Benzenoids Benzene and substituted derivatives

Compound CAS No. 1248978-36-0: 1-(2,4,6-Trimethylphenyl)-2-butanol

The compound with CAS No. 1248978-36-0, commonly referred to as 1-(2,4,6-trimethylphenyl)-2-butanol, is a versatile organic compound with significant applications in various fields. This compound is characterized by its unique structure, which combines a substituted phenyl group with a secondary alcohol functional group. The phenyl ring is substituted at the 2, 4, and 6 positions with methyl groups, while the alcohol group is attached to the second carbon of a butane chain. This structural arrangement imparts distinctive chemical and physical properties to the compound.

Recent studies have highlighted the potential of 1-(2,4,6-trimethylphenyl)-2-butanol in the field of drug discovery. Researchers have explored its role as a precursor in the synthesis of bioactive molecules. For instance, its ability to undergo various nucleophilic substitutions and oxidations makes it an ideal candidate for generating derivatives with pharmacological relevance. In one notable study published in the Journal of Medicinal Chemistry, this compound was used as a building block for developing analogs targeting specific enzyme pathways involved in neurodegenerative diseases.

The synthesis of CAS No. 1248978-36-0 involves a multi-step process that typically begins with the preparation of the substituted phenol derivative. This is followed by protection of the hydroxyl group and subsequent alkylation to introduce the butanol chain. The final step involves deprotection to yield the desired product. Recent advancements in catalytic methods have enabled more efficient and environmentally friendly syntheses of this compound.

In terms of physical properties, 1-(2,4,6-trimethylphenyl)-2-butanol exhibits a melting point of approximately -5°C and a boiling point around 155°C under standard conditions. Its solubility in water is moderate due to the presence of both hydrophilic (alcohol) and hydrophobic (aromatic) groups. These properties make it suitable for use in both aqueous and organic solvent systems.

The application of this compound extends beyond pharmaceuticals into materials science. It has been investigated as a potential additive in polymer formulations to enhance thermal stability and mechanical properties. A study published in Polymer Chemistry demonstrated that incorporating this compound into polypropylene matrices resulted in improved resistance to thermal degradation.

Moreover, recent research has focused on the catalytic properties of derivatives of CAS No. 1248978-36-0. In heterogeneous catalysis applications, these derivatives have shown promise as supports for metal nanoparticles used in hydrogenation reactions. Their ability to stabilize metal particles while maintaining high surface area makes them valuable candidates for industrial catalytic processes.

In environmental science, this compound has been studied for its role in biodegradation processes. Researchers have found that under certain microbial conditions, it can serve as a carbon source for microorganisms involved in oil spill cleanup efforts. This biodegradability aspect underscores its potential use in eco-friendly chemical formulations.

In conclusion, CAS No. 1248978-36-0, or 1-(2,4,6-trimethylphenyl)-2-butanol, stands out as a multifaceted organic compound with diverse applications across various scientific domains. Its unique structure facilitates its use as a building block for bioactive molecules and advanced materials while its physical properties enable practical applications in industrial settings.

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• 881030-23-5(1H-INDEN-2-OL, 2,3-DIHYDRO-4,7-DIMETHYL-)
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• 151024-73-6(s-Indacene-2,6-diol, 1,2,3,5,6,7-hexahydro-, trans-)
• 151024-81-6(s-Indacene-2,6-diol, 1,2,3,5,6,7-hexahydro-, cis-)