Cas no 28047-28-1 (A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL)
A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL Chemical and Physical Properties
Names and Identifiers
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- Benzenemethanol, a-cyclohexyl-4-methyl-
- A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL
- Cyclohexyl (4-methylphenyl)methanol
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- MDL: MFCD11935946
- Inchi: 1S/C14H20O/c1-11-7-9-13(10-8-11)14(15)12-5-3-2-4-6-12/h7-10,12,14-15H,2-6H2,1H3
- InChI Key: BRSIDGBKFUGJLX-UHFFFAOYSA-N
- SMILES: C(C1CCCCC1)(C1=CC=C(C)C=C1)O
Computed Properties
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 15
- Rotatable Bond Count: 2
A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| abcr | AB430039-1 g |
Cyclohexyl (4-methylphenyl)methanol |
28047-28-1 | 1g |
€602.60 | 2023-04-23 | ||
| SHANG HAI BI DE YI YAO KE JI GU FEN Co., Ltd. | BD593899-1g |
Cyclohexyl(p-tolyl)methanol |
28047-28-1 | 97% | 1g |
¥3549.0 | 2023-03-30 | |
| abcr | AB430039-1g |
Cyclohexyl (4-methylphenyl)methanol; . |
28047-28-1 | 1g |
€467.50 | 2025-02-17 | ||
| A2B Chem LLC | AX97398-1g |
Cyclohexyl (4-methylphenyl)methanol |
28047-28-1 | 97% | 1g |
$1205.00 | 2024-04-20 | |
| A2B Chem LLC | AX97398-5g |
Cyclohexyl (4-methylphenyl)methanol |
28047-28-1 | 97% | 5g |
$2831.00 | 2024-04-20 | |
| Ambeed | A631853-1g |
Cyclohexyl(p-tolyl)methanol |
28047-28-1 | 97% | 1g |
$517.0 | 2024-04-20 | |
| abcr | AB430039-5g |
Cyclohexyl (4-methylphenyl)methanol; . |
28047-28-1 | 5g |
€1534.30 | 2025-02-17 | ||
| abcr | AB430039-250mg |
Cyclohexyl (4-methylphenyl)methanol; . |
28047-28-1 | 250mg |
€260.30 | 2025-02-17 | ||
| abcr | AB430039-500mg |
Cyclohexyl (4-methylphenyl)methanol; . |
28047-28-1 | 500mg |
€348.90 | 2025-02-17 |
A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL Related Literature
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Xiaoming Liu,Zachary D. Hood,Wangda Li,Donovan N. Leonard,Arumugam Manthiram,Miaofang Chi J. Mater. Chem. A, 2021,9, 2111-2119
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Joseph W. Bennett,Diamond T. Jones,Blake G. Hudson,Joshua Melendez-Rivera,Robert J. Hamers,Sara E. Mason Environ. Sci.: Nano, 2020,7, 1642-1651
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Chung-Sung Yang,Mong-Shian Shih,Fang-Yi Chang New J. Chem., 2006,30, 729-735
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Brindha J.,Balamurali M. M.,Kaushik Chanda RSC Adv., 2019,9, 34720-34734
Additional information on A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL
Introduction to A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL (CAS No. 28047-28-1)
A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL, identified by its Chemical Abstracts Service (CAS) number 28047-28-1, is a significant compound in the realm of organic chemistry and pharmaceutical research. This molecule, characterized by its cyclohexyl and methyl substituents on a benzene ring, has garnered attention due to its unique structural properties and potential applications in medicinal chemistry. The presence of both aromatic and aliphatic moieties makes it a versatile intermediate, facilitating various synthetic pathways that are crucial for drug development.
The compound belongs to the class of benzyl alcohols, which are widely recognized for their role in synthesizing more complex molecules. Specifically, A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL serves as a building block in the construction of pharmacophores, which are key structural elements responsible for the biological activity of drugs. Its molecular structure allows for modifications at multiple sites, enabling chemists to tailor its properties for specific applications.
In recent years, there has been a surge in research focused on developing novel therapeutic agents with improved efficacy and reduced side effects. A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL has emerged as a valuable candidate in this context. Its ability to undergo various chemical reactions, such as oxidation and reduction, makes it a preferred choice for synthesizing derivatives that exhibit promising biological activities. For instance, researchers have explored its potential in developing anti-inflammatory agents, where its structural features contribute to enhanced binding affinity to target proteins.
The pharmaceutical industry has been particularly interested in A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL due to its role in the synthesis of active pharmaceutical ingredients (APIs). The compound's stability under different conditions and its compatibility with various synthetic protocols make it an ideal candidate for large-scale production. Moreover, advancements in green chemistry have prompted investigations into more sustainable methods for producing this compound, reducing the environmental impact of its synthesis.
One of the most intriguing aspects of A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL is its utility in the development of chiral compounds. The presence of a stereocenter allows for the creation of enantiomerically pure derivatives, which are often required for optimal pharmacological activity. Researchers have leveraged this property to develop novel drugs that target specific biological pathways with high selectivity. This has opened up new avenues in personalized medicine, where individual patient responses can be better predicted and managed.
Recent studies have also highlighted the role of A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL in drug delivery systems. Its structural features enable it to be incorporated into various formulations, including liposomes and nanoparticles, which enhance drug solubility and bioavailability. These advancements are particularly relevant in addressing challenges associated with poorly soluble drugs, improving their therapeutic efficacy.
The chemical synthesis of A-CYCLOHEXYL-4-METHYL-BENZENEMETHANOL involves multiple steps that require precise control over reaction conditions. Modern synthetic methodologies have enabled more efficient and scalable production processes. For example, catalytic hydrogenation techniques have been employed to introduce the cyclohexyl group efficiently, minimizing byproduct formation. Such innovations not only improve yield but also reduce costs associated with purification and isolation.
The versatility of A-CYCLOHEXYL-4-METHYLBENZENEMETHANOL extends beyond pharmaceutical applications. It has found utility in materials science, where its aromatic structure contributes to the development of high-performance polymers and coatings. These materials exhibit enhanced durability and chemical resistance, making them suitable for industrial applications requiring robust performance under harsh conditions.
In conclusion,A-CYCLOHEXYL-4-METHYLBENZENEMETHANOL (CAS No. 28047-28-1) is a multifaceted compound with significant implications across multiple domains of chemistry and medicine. Its unique structural features enable diverse applications, from drug development to advanced materials. As research continues to uncover new possibilities, this compound is poised to play an increasingly important role in addressing global challenges in health and technology.
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