Cas no 1511673-51-0 (4-1-(aminomethyl)cyclohexylphenol)
4-1-(aminomethyl)cyclohexylphenol Chemical and Physical Properties
Names and Identifiers
-
- 4-1-(aminomethyl)cyclohexylphenol
- Phenol, 4-[1-(aminomethyl)cyclohexyl]-
- 4-[1-(aminomethyl)cyclohexyl]phenol
- EN300-1850654
- 1511673-51-0
-
- Inchi: 1S/C13H19NO/c14-10-13(8-2-1-3-9-13)11-4-6-12(15)7-5-11/h4-7,15H,1-3,8-10,14H2
- InChI Key: AORWVHRZXFYANZ-UHFFFAOYSA-N
- SMILES: C1(O)=CC=C(C2(CN)CCCCC2)C=C1
Computed Properties
- Exact Mass: 205.146664230g/mol
- Monoisotopic Mass: 205.146664230g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 2
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 15
- Rotatable Bond Count: 2
- Complexity: 191
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.8
- Topological Polar Surface Area: 46.2?2
Experimental Properties
- Density: 1.067±0.06 g/cm3(Predicted)
- Boiling Point: 348.6±25.0 °C(Predicted)
- pka: 10.21±0.30(Predicted)
4-1-(aminomethyl)cyclohexylphenol Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Enamine | EN300-1850654-0.05g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 0.05g |
$528.0 | 2023-09-19 | ||
| Enamine | EN300-1850654-0.1g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 0.1g |
$553.0 | 2023-09-19 | ||
| Enamine | EN300-1850654-0.25g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 0.25g |
$579.0 | 2023-09-19 | ||
| Enamine | EN300-1850654-0.5g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 0.5g |
$603.0 | 2023-09-19 | ||
| Enamine | EN300-1850654-1.0g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 1g |
$928.0 | 2023-06-01 | ||
| Enamine | EN300-1850654-2.5g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 2.5g |
$1230.0 | 2023-09-19 | ||
| Enamine | EN300-1850654-5.0g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 5g |
$2692.0 | 2023-06-01 | ||
| Enamine | EN300-1850654-10.0g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 10g |
$3992.0 | 2023-06-01 | ||
| Enamine | EN300-1850654-1g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 1g |
$628.0 | 2023-09-19 | ||
| Enamine | EN300-1850654-5g |
4-[1-(aminomethyl)cyclohexyl]phenol |
1511673-51-0 | 5g |
$1821.0 | 2023-09-19 |
4-1-(aminomethyl)cyclohexylphenol Related Literature
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Alvin Tanudjaja,Shinsuke Inagi,Fusao Kitamura,Toshikazu Takata,Ikuyoshi Tomita Dalton Trans., 2021,50, 3037-3043
-
Bo Cao,Yin Wei Chem. Commun., 2018,54, 2870-2873
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Chengbin Yang,Hing Lun Tsang,Pui Man Lau,Ken-Tye Yong,Ho Pui Ho,Siu Kai Kong Analyst, 2017,142, 3579-3587
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Dhamodaran Manikandan,S. Amirthapandian,I. S. Zhidkov,A. I. Kukharenko,S. O. Cholakh,Ramaswamy Murugan Phys. Chem. Chem. Phys., 2018,20, 6500-6514
-
Chandran Rajendran,Govindaswamy Satishkumar,Charlotte Lang,Eric M. Gaigneaux Catal. Sci. Technol., 2020,10, 2583-2592
Additional information on 4-1-(aminomethyl)cyclohexylphenol
4-1-(Aminomethyl)cyclohexylphenol: A Comprehensive Overview
The compound with CAS No 1511673-51-0, commonly referred to as 4-1-(aminomethyl)cyclohexylphenol, is a versatile organic molecule that has garnered significant attention in recent years due to its unique properties and potential applications. This compound is a derivative of phenol, with a cyclohexyl group substituted at the para position and an aminomethyl group attached to the cyclohexane ring. Its structure allows for a wide range of chemical reactivity, making it a valuable intermediate in various synthetic processes.
4-1-(Aminomethyl)cyclohexylphenol has been extensively studied for its role in drug discovery and material science. Recent research has highlighted its potential as a building block for developing bioactive compounds, particularly in the field of medicinal chemistry. The presence of both phenolic and amine functionalities provides opportunities for hydrogen bonding, which is crucial for interactions with biological targets. This makes the compound an attractive candidate for designing drugs targeting various therapeutic areas, including inflammation, neurodegenerative diseases, and cancer.
In terms of synthesis, 4-1-(Aminomethyl)cyclohexylphenol can be prepared through several routes, including nucleophilic aromatic substitution and coupling reactions. These methods have been optimized in recent studies to improve yield and purity, ensuring that the compound is readily available for further exploration. The stability of the molecule under various reaction conditions has also been evaluated, making it suitable for large-scale production.
One of the most promising applications of 4-1-(Aminomethyl)cyclohexylphenol lies in its ability to act as a precursor for advanced materials. For instance, researchers have explored its use in polymer synthesis, where it serves as a functional monomer to create materials with tailored properties. The incorporation of this compound into polymer networks has been shown to enhance mechanical strength and thermal stability, opening avenues for its use in high-performance materials.
Moreover, 4-1-(Aminomethyl)cyclohexylphenol has been investigated for its environmental applications. Studies have demonstrated its effectiveness as a sorbent for heavy metal ions in contaminated water. The phenolic hydroxyl groups and amine functionalities provide multiple binding sites for metal ions, making this compound a potential solution for water purification technologies.
The safety profile of 4-1-(Aminomethyl)cyclohexylphenol has also been assessed in recent toxicity studies. Results indicate that the compound exhibits low toxicity at typical exposure levels, which is essential for its consideration in pharmaceutical and industrial applications. However, further long-term studies are recommended to fully understand its safety profile.
In conclusion, 4-1-(Aminomethyl)cyclohexylphenol (CAS No 1511673-51-0) is a multifaceted compound with diverse applications across various fields. Its unique chemical structure and functional groups make it an invaluable tool in drug discovery, material science, and environmental technology. As research continues to uncover new potentials for this compound, it is poised to play an increasingly important role in advancing scientific innovation.
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