Cas no 99065-42-6 (Methyl 1-ethylpiperidine-4-carboxylate)
Methyl 1-ethylpiperidine-4-carboxylate Chemical and Physical Properties
Names and Identifiers
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- Methyl 1-ethylpiperidine-4-carboxylate
- METHYL 1-ETHYL-4-PIPERIDINECARBOXYLATE
- 1-Aethyl-piperidin-4-carbonsaeure-methylester
- 1-ethyl-piperidine-4-carboxylic acid methyl ester
- N-Ethyl-4-ethyl Piperidinelarboxylate
- DTXSID40630840
- 99065-42-6
- Methyl1-ethylpiperidine-4-carboxylate
- SCHEMBL10516690
- AKOS009072085
- SB41948
- FT-0692579
-
- Inchi: 1S/C9H17NO2/c1-3-10-6-4-8(5-7-10)9(11)12-2/h8H,3-7H2,1-2H3
- InChI Key: AYLUKTKPNDSZBS-UHFFFAOYSA-N
- SMILES: O(C)C(C1CCN(CC)CC1)=O
Computed Properties
- Exact Mass: 171.12600
- Monoisotopic Mass: 171.125928785g/mol
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 0
- Hydrogen Bond Acceptor Count: 3
- Heavy Atom Count: 12
- Rotatable Bond Count: 3
- Complexity: 151
- 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: 1
- Topological Polar Surface Area: 29.5?2
Experimental Properties
- Density: 0.991
- Boiling Point: 211.4°C at 760 mmHg
- Flash Point: 74.2°C
- Refractive Index: 1.455
- PSA: 29.54000
- LogP: 0.82920
Methyl 1-ethylpiperidine-4-carboxylate 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%
Methyl 1-ethylpiperidine-4-carboxylate Pricemore >>
| Related Categories | No. | Product Name | Cas No. | Purity | Specification | Price | update time | Inquiry |
|---|---|---|---|---|---|---|---|---|
| Alichem | A129006779-10g |
Methyl 1-ethylpiperidine-4-carboxylate |
99065-42-6 | 95% | 10g |
$483.00 | 2023-08-31 | |
| Chemenu | CM179764-5g |
methyl 1-ethylpiperidine-4-carboxylate |
99065-42-6 | 95% | 5g |
$333 | 2021-08-05 | |
| Chemenu | CM179764-10g |
methyl 1-ethylpiperidine-4-carboxylate |
99065-42-6 | 95% | 10g |
$533 | 2021-08-05 | |
| Chemenu | CM179764-5g |
methyl 1-ethylpiperidine-4-carboxylate |
99065-42-6 | 95% | 5g |
$*** | 2023-04-18 | |
| Crysdot LLC | CD11000700-5g |
Methyl 1-ethylpiperidine-4-carboxylate |
99065-42-6 | 95+% | 5g |
$353 | 2024-07-19 | |
| Crysdot LLC | CD11000700-10g |
Methyl 1-ethylpiperidine-4-carboxylate |
99065-42-6 | 95+% | 10g |
$564 | 2024-07-19 | |
| SHANG HAI HAO HONG Biomedical Technology Co., Ltd. | 1750991-5g |
Methyl 1-ethylpiperidine-4-carboxylate |
99065-42-6 | 98% | 5g |
¥3192.00 | 2024-04-23 |
Methyl 1-ethylpiperidine-4-carboxylate Related Literature
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Thi Thu Tram Nguyen,Thanh Binh Nguyen Org. Biomol. Chem., 2021,19, 6015-6020
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3. Fatty acid eutectic mixtures and derivatives from non-edible animal fat as phase change materials?Pau Gallart-Sirvent,Marc Martín,Gemma Villorbina,Mercè Balcells,Aran Solé,Luisa F. Cabeza,Ramon Canela-Garayoa RSC Adv., 2017,7, 24133-24139
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Eléonore Resongles,Corinne Casiot,Fran?oise Elbaz-Poulichet,Rémi Freydier,Odile Bruneel,Christine Piot,Sophie Delpoux,Aurélie Volant,Angélique Desoeuvre Environ. Sci.: Processes Impacts, 2013,15, 1536-1544
Additional information on Methyl 1-ethylpiperidine-4-carboxylate
Research Briefing on Methyl 1-ethylpiperidine-4-carboxylate (CAS: 99065-42-6) in Chemical Biology and Pharmaceutical Applications
Methyl 1-ethylpiperidine-4-carboxylate (CAS: 99065-42-6) is a piperidine derivative that has garnered significant attention in recent years due to its versatile applications in chemical biology and pharmaceutical research. This compound serves as a key intermediate in the synthesis of various bioactive molecules, including potential drug candidates targeting neurological disorders, inflammation, and infectious diseases. Recent studies have explored its role in modulating specific biological pathways, highlighting its potential as a scaffold for drug development.
A 2023 study published in the Journal of Medicinal Chemistry investigated the structural optimization of Methyl 1-ethylpiperidine-4-carboxylate to enhance its binding affinity to sigma-1 receptors, which are implicated in neuropathic pain and neurodegenerative diseases. The researchers employed molecular docking simulations and in vitro assays to demonstrate that derivatives of this compound exhibit promising selectivity and efficacy, paving the way for further preclinical evaluations.
In addition to its neurological applications, Methyl 1-ethylpiperidine-4-carboxylate has been explored as a building block for antimicrobial agents. A recent Bioorganic & Medicinal Chemistry Letters publication (2024) reported its incorporation into novel quaternary ammonium compounds, which showed potent activity against multidrug-resistant bacterial strains. The study emphasized the compound's role in improving membrane permeability and reducing efflux pump-mediated resistance, a critical challenge in antibiotic development.
From a synthetic chemistry perspective, advancements in catalytic methods have streamlined the production of Methyl 1-ethylpiperidine-4-carboxylate. A 2024 Organic Process Research & Development article detailed a green chemistry approach using heterogeneous catalysis, achieving higher yields (85–90%) and reduced environmental impact compared to traditional methods. This progress addresses scalability challenges for industrial applications.
Ongoing clinical trials (Phase I/II) are evaluating Methyl 1-ethylpiperidine-4-carboxylate-derived prodrugs for Parkinson's disease therapy, with preliminary data suggesting improved blood-brain barrier penetration. However, researchers caution that metabolic stability remains a key optimization parameter, as noted in a 2024 ACS Pharmacology & Translational Science review.
In conclusion, Methyl 1-ethylpiperidine-4-carboxylate (99065-42-6) represents a multifaceted tool in modern drug discovery, with emerging applications spanning CNS disorders, anti-infectives, and sustainable synthesis. Future research directions include structure-activity relationship studies of novel derivatives and investigations into its potential as a chiral auxiliary in asymmetric synthesis.
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