Cas no 17293-45-7 (2-Phenylcyclohexanamine)
2-Phenylcyclohexanamine Chemical and Physical Properties
Names and Identifiers
-
- Cyclohexanamine, 2-phenyl-
- 2-phenylcyclohexan-1-amine
- DTXSID20337840
- 2-phenylcyclohexylamine
- 2-Phenyl-cyclohexylamine
- Z446021014
- CS-0269900
- 17293-45-7
- SCHEMBL445956
- 2-Phenylcyclohexanamine #
- 2-Phenylcyclohexanamine
- 2-Phenylcyclohexylamin
- EN300-54527
- AKOS009939583
-
- Inchi: 1S/C12H17N/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-3,6-7,11-12H,4-5,8-9,13H2
- InChI Key: KLJIPLWGNJQJRM-UHFFFAOYSA-N
- SMILES: NC1CCCCC1C1C=CC=CC=1
Computed Properties
- Exact Mass: 175.13621
- Monoisotopic Mass: 175.136099547g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 1
- Heavy Atom Count: 13
- Rotatable Bond Count: 1
- Complexity: 149
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 2
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.5
- Topological Polar Surface Area: 26?2
Experimental Properties
- PSA: 26.02
2-Phenylcyclohexanamine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P400258-25mg |
2-Phenylcyclohexanamine |
17293-45-7 | 25mg |
$ 70.00 | 2022-06-03 | ||
| TRC | P400258-50mg |
2-Phenylcyclohexanamine |
17293-45-7 | 50mg |
$ 95.00 | 2022-06-03 | ||
| TRC | P400258-250mg |
2-Phenylcyclohexanamine |
17293-45-7 | 250mg |
$ 340.00 | 2022-06-03 | ||
| Enamine | EN300-54527-0.05g |
2-phenylcyclohexan-1-amine |
17293-45-7 | 0.05g |
$66.0 | 2023-02-10 | ||
| Enamine | EN300-54527-0.1g |
2-phenylcyclohexan-1-amine |
17293-45-7 | 0.1g |
$98.0 | 2023-02-10 | ||
| Enamine | EN300-54527-0.25g |
2-phenylcyclohexan-1-amine |
17293-45-7 | 0.25g |
$142.0 | 2023-02-10 | ||
| Enamine | EN300-54527-0.5g |
2-phenylcyclohexan-1-amine |
17293-45-7 | 0.5g |
$271.0 | 2023-02-10 | ||
| Enamine | EN300-54527-1.0g |
2-phenylcyclohexan-1-amine |
17293-45-7 | 1.0g |
$371.0 | 2023-02-10 | ||
| Enamine | EN300-54527-2.5g |
2-phenylcyclohexan-1-amine |
17293-45-7 | 2.5g |
$726.0 | 2023-02-10 | ||
| Enamine | EN300-54527-5.0g |
2-phenylcyclohexan-1-amine |
17293-45-7 | 5.0g |
$1074.0 | 2023-02-10 |
2-Phenylcyclohexanamine Related Literature
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Siquan Zhang,Shengyao Wang,Liping Guo,Hao Chen,Bien Tan,Shangbin Jin J. Mater. Chem. C, 2020,8, 192-200
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M. T. Colomer,S. Díaz-Moreno,A. Tamayo,A. L. Ortiz J. Mater. Chem. C, 2018,6, 12643-12651
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Huifang Yang,Haoran Guo,Peidong Fan,Xinpan Li,Wenlu Ren,Rui Song Nanoscale, 2020,12, 7024-7034
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Xiang Liu,Qian Sun,A. B. Djuri?i?,Maohai Xie,Baohu Dai,Jinyao Tang,Charles Surya,Changzhong Liao,Kaimin Shih RSC Adv., 2015,5, 100783-100789
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Robert J. Meagher,Anson V. Hatch,Ronald F. Renzi,Anup K. Singh Lab Chip, 2008,8, 2046-2053
Additional information on 2-Phenylcyclohexanamine
Cyclohexanamine, 2-phenyl- (CAS No. 17293-45-7): Properties, Applications, and Market Insights
Cyclohexanamine, 2-phenyl- (CAS No. 17293-45-7), also known as 2-phenylcyclohexylamine, is a versatile organic compound with a wide range of applications in pharmaceuticals, agrochemicals, and specialty chemicals. Its unique chemical structure, featuring a cyclohexylamine backbone substituted with a phenyl group, makes it a valuable intermediate in synthetic chemistry. This article delves into the properties, applications, and market trends of this compound, addressing common queries and industry trends.
The molecular formula of Cyclohexanamine, 2-phenyl- is C12H17N, with a molecular weight of 175.27 g/mol. Its structure combines the rigidity of the phenyl ring with the flexibility of the cyclohexane ring, offering unique reactivity. Researchers often explore its potential in chiral synthesis due to its stereogenic center, making it a topic of interest in asymmetric catalysis and drug development.
One of the most searched questions about Cyclohexanamine, 2-phenyl- is its role in pharmaceutical intermediates. Recent studies highlight its use in the synthesis of bioactive molecules, particularly in central nervous system (CNS) targeting drugs. The compound's ability to act as a building block for neuroactive compounds aligns with the growing demand for mental health therapeutics, a trending topic in 2024.
In agrochemical applications, 2-phenylcyclohexylamine derivatives have shown promise as crop protection agents. With the global focus on sustainable agriculture, researchers are investigating its potential in eco-friendly pest control solutions. This aligns with the increasing search queries around green chemistry and biodegradable agrochemicals.
The synthesis of Cyclohexanamine, 2-phenyl- typically involves the reduction of 2-phenylcyclohexanone or reductive amination strategies. Recent advancements in catalytic hydrogenation methods have improved the efficiency of its production, addressing industry demands for cost-effective and scalable processes. These developments are frequently discussed in forums focusing on process optimization and industrial chemistry.
Market analysis reveals steady growth for Cyclohexanamine, 2-phenyl-, driven by its pharmaceutical applications. The compound's suppliers often highlight its >98% purity grades, catering to the stringent requirements of GMP manufacturing. With the rise of contract research organizations (CROs), the demand for high-quality intermediates like 2-phenylcyclohexylamine continues to increase.
From a regulatory perspective, Cyclohexanamine, 2-phenyl- is generally regarded as safe when handled properly, with standard organic compound precautions. Safety data sheets emphasize proper ventilation and personal protective equipment, reflecting the industry's focus on laboratory safety protocols - a hot topic in chemical education circles.
Innovative applications of Cyclohexanamine, 2-phenyl- are emerging in material science, particularly in the development of specialty polymers. Its incorporation into polymer backbones can modify thermal and mechanical properties, making it relevant to searches about advanced materials and smart coatings.
Analytical characterization of 2-phenylcyclohexylamine typically involves techniques like GC-MS, HPLC, and NMR spectroscopy. Method development for its quantification remains an active research area, as evidenced by frequent queries about analytical method validation in chemical forums.
Storage recommendations for Cyclohexanamine, 2-phenyl- suggest keeping it in cool, dry conditions away from oxidizing agents. These guidelines align with best practices for chemical storage, a subject of increasing importance in facility management discussions.
The future outlook for Cyclohexanamine, 2-phenyl- appears promising, with research exploring its potential in catalysis and medicinal chemistry. As synthetic methodologies advance and new applications emerge, this compound continues to attract attention from both academic and industrial researchers worldwide.
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