Cas no 99065-42-6 (Methyl 1-ethylpiperidine-4-carboxylate)

Methyl 1-ethylpiperidine-4-carboxylate is a piperidine derivative with a methyl ester functional group at the 4-position and an ethyl substituent on the nitrogen atom. This compound serves as a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable for constructing complex molecules. The ester group enhances solubility in organic solvents, facilitating reactions such as hydrolysis, reduction, or amidation. The ethyl substitution on the nitrogen influences steric and electronic properties, which can be tailored for specific applications. This compound is typically handled under standard laboratory conditions, requiring appropriate storage to maintain stability.
Methyl 1-ethylpiperidine-4-carboxylate structure
99065-42-6 structure
Product Name:Methyl 1-ethylpiperidine-4-carboxylate
CAS No:99065-42-6
MF:C9H17NO2
MW:171.23678278923
CID:1039645
PubChem ID:23126634
Update Time:2025-09-25

Methyl 1-ethylpiperidine-4-carboxylate Chemical and Physical Properties

Names and Identifiers

    • 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:

    2933399090

    Overview:

    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

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.

Recommended suppliers
Yunnanjiuzhen
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Yunnanjiuzhen
Shandong Feiyang Chemical Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Shandong Feiyang Chemical Co., Ltd
ASIACHEM I&E (JIANGSU) CO., LTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
ASIACHEM I&E (JIANGSU) CO., LTD
Inner Mongolia Xinhong Biological Technology Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Inner Mongolia Xinhong Biological Technology Co., Ltd
Enjia Trading Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Enjia Trading Co., Ltd