Cas no 955315-04-5 (3-(4-Ethoxybenzyl)piperidine)
3-(4-Ethoxybenzyl)piperidine Chemical and Physical Properties
Names and Identifiers
-
- 3-(4-Ethoxybenzyl)piperidine
- 3-(4-ETHOXY-BENZYL)-PIPERIDINE
- 3-[(4-ethoxyphenyl)methyl]piperidine
- 955315-04-5
- DTXSID30588801
- EN300-1868079
- FT-0681581
- AB22590
- AKOS012086513
- BB 0262617
-
- MDL: MFCD05863595
- Inchi: 1S/C14H21NO/c1-2-16-14-7-5-12(6-8-14)10-13-4-3-9-15-11-13/h5-8,13,15H,2-4,9-11H2,1H3
- InChI Key: RSACBNWSKVWJRW-UHFFFAOYSA-N
- SMILES: O(CC)C1C=CC(=CC=1)CC1CNCCC1
Computed Properties
- Exact Mass: 219.16200
- Monoisotopic Mass: 219.162314293g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 2
- Heavy Atom Count: 16
- Rotatable Bond Count: 4
- Complexity: 187
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- XLogP3: 2.8
- Topological Polar Surface Area: 21.3?2
Experimental Properties
- PSA: 21.26000
- LogP: 2.95620
3-(4-Ethoxybenzyl)piperidine Customs Data
- HS CODE:2933399090
- Customs Data:
China Customs Code:
2933399090Overview:
2933399090. Other compounds with non fused pyridine rings in structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%
Declaration elements:
Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date
Summary:
2933399090. other compounds containing an unfused pyridine ring (whether or not hydrogenated) in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%
3-(4-Ethoxybenzyl)piperidine Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | E940685-5mg |
3-(4-Ethoxybenzyl)piperidine |
955315-04-5 | 5mg |
$ 50.00 | 2022-06-05 | ||
| TRC | E940685-10mg |
3-(4-Ethoxybenzyl)piperidine |
955315-04-5 | 10mg |
$ 65.00 | 2022-06-05 | ||
| TRC | E940685-50mg |
3-(4-Ethoxybenzyl)piperidine |
955315-04-5 | 50mg |
$ 135.00 | 2022-06-05 | ||
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 053703-500mg |
3-(4-Ethoxybenzyl)piperidine |
955315-04-5 | 500mg |
1576CNY | 2021-05-07 | ||
| Chemenu | CM530861-1g |
3-(4-Ethoxybenzyl)piperidine |
955315-04-5 | 95% | 1g |
$149 | 2022-08-31 | |
| Chemenu | CM530861-5g |
3-(4-Ethoxybenzyl)piperidine |
955315-04-5 | 95% | 5g |
$446 | 2022-08-31 | |
| SHANG HAI XIAN DING Biotechnology Co., Ltd. | 053703-500mg |
3-(4-Ethoxybenzyl)piperidine |
955315-04-5 | 500mg |
1576.0CNY | 2021-07-13 | ||
| Enamine | EN300-1868079-0.05g |
3-[(4-ethoxyphenyl)methyl]piperidine |
955315-04-5 | 0.05g |
$107.0 | 2023-09-18 | ||
| Enamine | EN300-1868079-0.1g |
3-[(4-ethoxyphenyl)methyl]piperidine |
955315-04-5 | 0.1g |
$112.0 | 2023-09-18 | ||
| Enamine | EN300-1868079-0.25g |
3-[(4-ethoxyphenyl)methyl]piperidine |
955315-04-5 | 0.25g |
$117.0 | 2023-09-18 |
3-(4-Ethoxybenzyl)piperidine Related Literature
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Supaporn Sawadjoon,Joseph S. M. Samec Org. Biomol. Chem., 2011,9, 2548-2554
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Juan J. Sánchez,Miguel López-Haro,Juan C. Hernández-Garrido,Ginesa Blanco,Miguel A. Cauqui,José M. Rodríguez-Izquierdo,José A. Pérez-Omil,José J. Calvino,María P. Yeste J. Mater. Chem. A, 2019,7, 8993-9003
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Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Hyejin Moon,Aaron R. Wheeler,Robin L. Garrell,Chang-Jin “CJ” Kim Lab Chip, 2006,6, 1213-1219
Additional information on 3-(4-Ethoxybenzyl)piperidine
Introduction to 3-(4-Ethoxybenzyl)piperidine (CAS No. 955315-04-5)
3-(4-Ethoxybenzyl)piperidine, with the CAS number 955315-04-5, is a synthetic compound that has garnered significant attention in the fields of medicinal chemistry and pharmaceutical research. This compound is characterized by its unique structural features, which include a piperidine ring and a 4-ethoxybenzyl substituent. These structural elements contribute to its potential pharmacological properties and make it a valuable candidate for various applications, particularly in the development of novel therapeutic agents.
The chemical structure of 3-(4-Ethoxybenzyl)piperidine can be represented as C14H21NO2. The presence of the piperidine ring, a six-membered cyclic amine, imparts basic properties to the molecule, while the 4-ethoxybenzyl group adds aromatic and ether functionalities. These combined features make 3-(4-Ethoxybenzyl)piperidine a versatile compound with potential interactions with various biological targets.
In recent years, significant advancements have been made in understanding the biological activities and potential therapeutic applications of 3-(4-Ethoxybenzyl)piperidine. Research has shown that this compound exhibits promising activity in several areas, including central nervous system (CNS) disorders, pain management, and neurodegenerative diseases. For instance, studies have demonstrated that 3-(4-Ethoxybenzyl)piperidine can modulate neurotransmitter systems, such as serotonin and dopamine, which are crucial for maintaining brain function and mood regulation.
The pharmacological profile of 3-(4-Ethoxybenzyl)piperidine has been extensively studied using both in vitro and in vivo models. In vitro assays have revealed that this compound can selectively bind to specific receptors, such as serotonin receptors (5-HT2A) and dopamine receptors (D2). These interactions suggest potential applications in treating conditions like depression, anxiety, and schizophrenia. Furthermore, preclinical studies have shown that 3-(4-Ethoxybenzyl)piperidine can cross the blood-brain barrier efficiently, enhancing its therapeutic potential for CNS disorders.
Beyond its role in CNS disorders, 3-(4-Ethoxybenzyl)piperidine has also shown promise in pain management. Research indicates that this compound can interact with nociceptive pathways and reduce pain sensitivity. This property makes it a potential candidate for developing new analgesic drugs that could offer improved efficacy and reduced side effects compared to existing treatments.
In the context of neurodegenerative diseases, such as Alzheimer's disease and Parkinson's disease, 3-(4-Ethoxybenzyl)piperidine has been investigated for its neuroprotective effects. Studies have shown that this compound can reduce oxidative stress and inflammation in neuronal cells, which are key factors contributing to neurodegeneration. Additionally, it has been found to enhance cognitive function in animal models of these diseases, suggesting its potential as a therapeutic agent for improving cognitive decline.
The synthesis of 3-(4-Ethoxybenzyl)piperidine involves several well-established chemical reactions. One common approach is the nucleophilic substitution of a halide on a benzene ring with an ethoxide ion to form the 4-ethoxybenzyl intermediate. This intermediate is then coupled with a piperidine derivative through a suitable coupling reaction to yield the final product. The synthetic route is highly reproducible and can be scaled up for industrial production.
The safety profile of 3-(4-Ethoxybenzyl)piperidine has been evaluated through extensive toxicological studies. These studies have shown that the compound is generally well-tolerated at therapeutic doses and exhibits low toxicity. However, like any pharmaceutical agent, it is important to conduct thorough clinical trials to ensure its safety and efficacy in human subjects.
In conclusion, 3-(4-Ethoxybenzyl)piperidine (CAS No. 955315-04-5) is a promising compound with a wide range of potential applications in medicinal chemistry and pharmaceutical research. Its unique structural features and pharmacological properties make it an attractive candidate for developing novel therapeutic agents for CNS disorders, pain management, and neurodegenerative diseases. Ongoing research continues to uncover new insights into its mechanisms of action and therapeutic potential, further solidifying its importance in the field.
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