Cas no 1220037-77-3 (2-(3-Piperidinyl)ethyl propanoate hydrochloride)
2-(3-Piperidinyl)ethyl propanoate hydrochloride Chemical and Physical Properties
Names and Identifiers
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- 2-(3-Piperidinyl)ethyl propanoate hydrochloride
- AKOS015846634
- 2-(Piperidin-3-yl)ethylpropionatehydrochloride
- 1220037-77-3
- 2-(Piperidin-3-yl)ethyl propionate hydrochloride
- 2-piperidin-3-ylethyl propanoate;hydrochloride
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- MDL: MFCD13559771
- Inchi: 1S/C10H19NO2.ClH/c1-2-10(12)13-7-5-9-4-3-6-11-8-9;/h9,11H,2-8H2,1H3;1H
- InChI Key: CHZRGMBLWTYYBD-UHFFFAOYSA-N
- SMILES: Cl.O(C(CC)=O)CCC1CNCCC1
Computed Properties
- Exact Mass: 221.1182566g/mol
- Monoisotopic Mass: 221.1182566g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 1
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 14
- Rotatable Bond Count: 5
- Complexity: 159
- Covalently-Bonded Unit Count: 2
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 1
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 38.3?2
2-(3-Piperidinyl)ethyl propanoate hydrochloride Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| TRC | P034025-125mg |
2-(3-Piperidinyl)ethyl propanoate hydrochloride |
1220037-77-3 | 125mg |
$ 230.00 | 2022-06-03 | ||
| TRC | P034025-250mg |
2-(3-Piperidinyl)ethyl propanoate hydrochloride |
1220037-77-3 | 250mg |
$ 375.00 | 2022-06-03 |
2-(3-Piperidinyl)ethyl propanoate hydrochloride Related Literature
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Muniyandi Sankaralingam,So Hyun Jeon,Yong-Min Lee,Mi Sook Seo,Wonwoo Nam Dalton Trans., 2016,45, 376-383
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Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
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3. An amorphous lanthanum–iridium solid solution with an open structure for efficient water splitting?Wei Sun,Chenglong Ma,Xinlong Tian,Jianjun Liao,Ji Yang,Chengjun Ge,Weiwei Huang J. Mater. Chem. A, 2020,8, 12518-12525
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Xixi Li,Nanwei Zhu,Ruohan Li,Qinpu Zhang Anal. Methods, 2020,12, 3376-3381
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Kanjun Sun,Fengting Hua,Shuzhen Cui,Yanrong Zhu,Hui Peng,Guofu Ma RSC Adv., 2021,11, 37631-37642
Additional information on 2-(3-Piperidinyl)ethyl propanoate hydrochloride
Professional Introduction to 2-(3-Piperidinyl)ethyl propanoate hydrochloride (CAS No: 1220037-77-3)
2-(3-Piperidinyl)ethyl propanoate hydrochloride, identified by the Chemical Abstracts Service Number (CAS No) 1220037-77-3, is a compound of significant interest in the field of pharmaceutical chemistry and medicinal research. This compound, featuring a piperidine moiety linked to an ethyl propanoate ester group and subsequently hydrochlorinated, exhibits a unique structural framework that has garnered attention for its potential biological activities and mechanistic applications.
The structural composition of 2-(3-Piperidinyl)ethyl propanoate hydrochloride positions it as a candidate for further exploration in drug discovery, particularly in the context of central nervous system (CNS) modulation and potential therapeutic interventions. The presence of the piperidine ring is a hallmark of many pharmacologically active agents, known for its ability to interact with various biological targets due to its favorable lipophilicity and metabolic stability. This feature, combined with the propanoate ester moiety, contributes to the compound's solubility profile and pharmacokinetic properties, making it an attractive scaffold for medicinal chemists.
In recent years, there has been growing interest in the development of novel compounds targeting neurological disorders. Piperidine derivatives have been extensively studied for their role in modulating neurotransmitter systems, particularly those involving dopamine, serotonin, and norepinephrine. The ethyl propanoate ester group in 2-(3-Piperidinyl)ethyl propanoate hydrochloride may contribute to its ability to cross the blood-brain barrier, a critical factor for CNS drugs. Furthermore, the hydrochloride salt form enhances the compound's stability and bioavailability, which are essential attributes for any candidate drug molecule.
Current research in the pharmaceutical industry emphasizes the need for innovative molecules with improved efficacy and reduced side effects. The structure-activity relationship (SAR) of 2-(3-Piperidinyl)ethyl propanoate hydrochloride has been a focus of several studies aimed at optimizing its pharmacological profile. Computational modeling and high-throughput screening techniques have been employed to evaluate its interactions with potential biological targets. These studies suggest that the compound may exhibit properties relevant to conditions such as depression, anxiety, and cognitive disorders.
One of the most compelling aspects of 2-(3-Piperidinyl)ethyl propanoate hydrochloride is its potential as a tool compound in biochemical research. Its well-defined structure allows researchers to investigate specific mechanisms of action at the molecular level. For instance, studies have explored its interactions with enzymes and receptors involved in neurotransmitter metabolism. Such investigations not only provide insights into the compound's mode of action but also contribute to our understanding of related diseases and potential therapeutic strategies.
The synthesis of 2-(3-Piperidinyl)ethyl propanoate hydrochloride involves multi-step organic reactions that highlight the expertise required in medicinal chemistry. Key synthetic steps include nucleophilic substitution reactions to introduce the piperidine moiety, esterification to form the propanoate group, and salt formation with hydrochloric acid. Advanced synthetic methodologies have been employed to ensure high yield and purity, which are crucial for preclinical and clinical studies.
Preclinical studies have begun to unravel the pharmacological potential of 2-(3-Piperidinyl)ethyl propanoate hydrochloride. In vitro assays have demonstrated its ability to modulate certain neurotransmitter pathways, suggesting therapeutic relevance for neurological conditions. Animal models have further supported these findings by showing promising effects on behavior and physiological parameters associated with CNS disorders. These preliminary results have laid the groundwork for more extensive clinical trials aimed at validating its efficacy and safety profiles.
The regulatory landscape for novel pharmaceutical compounds requires rigorous evaluation before they can enter clinical use. 2-(3-Piperidinyl)ethyl propanoate hydrochloride is currently undergoing comprehensive toxicological assessments to ensure its safety profile meets regulatory standards. These studies include acute toxicity tests, chronic toxicity evaluations, and genotoxicity assessments. The outcomes of these studies will be critical in determining whether this compound progresses into human clinical trials.
From a commercial perspective, the development of 2-(3-Piperidinyl)ethyl propanoate hydrochloride represents an investment in future healthcare solutions. Pharmaceutical companies are increasingly seeking innovative compounds that address unmet medical needs. The unique properties of this compound position it as a promising candidate for licensing or further development by industry players committed to advancing therapeutic options for neurological disorders.
The future direction of research on 2-(3-Piperidinyl)ethyl propanoate hydrochloride includes exploring its potential in combination therapies and investigating long-term effects through chronic administration studies. Additionally, advancements in drug delivery systems may enhance its bioavailability and targeted action within the CNS. Collaborative efforts between academic institutions and pharmaceutical industries will be essential in translating laboratory findings into tangible therapeutic benefits for patients.
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