Cas no 52253-93-7 ((3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate)

(3,3,5-Trimethylcyclohexyl) 2-hydroxybenzoate is a cycloaliphatic ester derived from salicylic acid, combining the structural stability of a trimethylcyclohexyl moiety with the functional versatility of a hydroxybenzoate group. This compound exhibits notable solubility in organic solvents, making it suitable for applications in polymer stabilizers, UV absorbers, and specialty coatings. Its sterically hindered cyclohexyl backbone enhances thermal and oxidative stability, while the phenolic hydroxyl group provides reactivity for further chemical modifications. The balanced lipophilicity and hydrolytic resistance of this ester contribute to its utility in formulations requiring prolonged shelf life and controlled release. Its compatibility with hydrophobic matrices further extends its use in high-performance material science applications.
(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate structure
52253-93-7 structure
Product Name:(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate
CAS No:52253-93-7
MF:C16H22O3
MW:262.344085216522
CID:1579956
Update Time:2026-04-28

(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate Chemical and Physical Properties

Names and Identifiers

    • LogP
    • (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate
    • Homomenthyl salicylate

Computed Properties

  • Exact Mass: 262.15696

Experimental Properties

  • PSA: 46.53

(3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
City Chemical
H512-100GM
Homomenthyl Salicylate
52253-93-7
100gm
$67.81 2023-09-19
City Chemical
H512-500GM
Homomenthyl Salicylate
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500gm
$210.61 2023-09-19
City Chemical
H512-18KG
Homomenthyl Salicylate
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$828.93 2023-09-19

Additional information on (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate

The Compound CAS No. 52253-93-7: (3,3,5-Trimethylcyclohexyl) 2-Hydroxybenzoate

The compound with CAS No. 52253-93-7, commonly referred to as (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate, is a unique organic compound that has garnered attention in various scientific and industrial applications. This compound is characterized by its complex structure, which combines a cyclohexyl group with a hydroxybenzoate moiety. The presence of the hydroxyl group in the benzoate portion imparts specific chemical and physical properties that make this compound versatile for different uses.

Recent studies have highlighted the potential of (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate in the field of materials science. Researchers have explored its ability to act as a precursor for the synthesis of advanced polymers and composites. The hydroxyl group in the molecule plays a crucial role in enabling strong intermolecular interactions, which can enhance the mechanical and thermal properties of the resulting materials. This makes it a promising candidate for applications in high-performance plastics and fibers.

In addition to its role in materials science, this compound has also been investigated for its potential in pharmaceuticals. The hydroxyl group in the benzoate moiety can undergo various chemical modifications to create derivatives with bioactive properties. For instance, recent research has focused on its ability to serve as a building block for drug delivery systems. The hydroxyl group can be functionalized to attach drugs or targeting molecules, enabling precise delivery of therapeutic agents to specific sites in the body.

The synthesis of (3,3,5-trimethylcyclohexyl) 2-hydroxybenzoate typically involves multi-step organic reactions. One common approach is the esterification of 2-hydroxybenzoic acid with (3,3,5-trimethylcyclohexanol). This reaction is often carried out under acidic conditions using a catalyst such as sulfuric acid or p-toluenesulfonic acid. The reaction conditions are optimized to maximize yield and purity of the final product.

From an environmental perspective, there has been growing interest in understanding the biodegradation and toxicity profiles of this compound. Recent studies have shown that under certain environmental conditions, such as those found in wastewater treatment systems or soil environments, this compound can undergo microbial degradation. However, further research is needed to fully understand its long-term environmental impact and potential risks.

In conclusion, CAS No. 52253-93-7 represents a versatile compound with diverse applications across multiple industries. Its unique structure and functional groups make it an attractive target for both academic research and industrial development. As new findings emerge from ongoing studies, it is expected that this compound will continue to play a significant role in advancing technologies and innovations across various fields.

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