Cas no 133567-09-6 (methyl cis-3-methylpiperidine-4-carboxylate)

methyl cis-3-methylpiperidine-4-carboxylate structure
133567-09-6 structure
Product Name:methyl cis-3-methylpiperidine-4-carboxylate
CAS No:133567-09-6
MF:C8H15NO2
MW:157.210202455521
CID:4483954
PubChem ID:14869354
Update Time:2025-10-29

methyl cis-3-methylpiperidine-4-carboxylate Chemical and Physical Properties

Names and Identifiers

    • 4-Piperidinecarboxylic acid, 3-methyl-, methyl ester, (3R,4R)-rel-
    • methyl (3R,4R)-3-methylpiperidine-4-carboxylate
    • methyl cis-3-methylpiperidine-4-carboxylate
    • SB42797
    • methyl trans-3-methylpiperidine-4-carboxylate
    • EN300-152219
    • SCHEMBL3976273
    • 133567-09-6
    • 1932258-80-4
    • AKOS023837847
    • F98309
    • 845909-33-3
    • 133567-11-0
    • methyl 3-methylpiperidine-4-carboxylate
    • starbld0000576
    • DA-02443
    • Inchi: 1S/C8H15NO2/c1-6-5-9-4-3-7(6)8(10)11-2/h6-7,9H,3-5H2,1-2H3/t6-,7+/m0/s1
    • InChI Key: BSPJTLUXMCHYGU-NKWVEPMBSA-N
    • SMILES: N1CC[C@@H](C(OC)=O)[C@@H](C)C1

Computed Properties

  • Exact Mass: 157.110278721Da
  • Monoisotopic Mass: 157.110278721Da
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 147
  • 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: 0.6
  • Topological Polar Surface Area: 38.3?2

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Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
NAN JING YAO SHI KE JI GU FEN Co., Ltd.
PBWB100389-100MG
methyl cis-3-methylpiperidine-4-carboxylate
133567-09-6 95%
100MG
¥ 1,089.00 2023-04-06
NAN JING YAO SHI KE JI GU FEN Co., Ltd.
PBWB100389-250MG
methyl cis-3-methylpiperidine-4-carboxylate
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¥ 1,742.00 2023-04-06
NAN JING YAO SHI KE JI GU FEN Co., Ltd.
PBWB100389-500MG
methyl cis-3-methylpiperidine-4-carboxylate
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500MG
¥ 2,904.00 2023-04-06
NAN JING YAO SHI KE JI GU FEN Co., Ltd.
PBWB100389-1G
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133567-09-6 95%
1g
¥ 4,349.00 2023-04-06
NAN JING YAO SHI KE JI GU FEN Co., Ltd.
PBWB100389-5G
methyl cis-3-methylpiperidine-4-carboxylate
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¥ 13,048.00 2023-04-06
NAN JING YAO SHI KE JI GU FEN Co., Ltd.
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NAN JING YAO SHI KE JI GU FEN Co., Ltd.
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NAN JING YAO SHI KE JI GU FEN Co., Ltd.
PBWB100389-250mg
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¥1711.0 2024-04-24
NAN JING YAO SHI KE JI GU FEN Co., Ltd.
PBWB100389-500mg
methyl cis-3-methylpiperidine-4-carboxylate
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Additional information on methyl cis-3-methylpiperidine-4-carboxylate

Exploring Methyl cis-3-Methylpiperidine-4-Carboxylate (CAS No. 133567-09-6): Properties, Applications, and Market Insights

Methyl cis-3-methylpiperidine-4-carboxylate (CAS No. 133567-09-6) is a specialized organic compound that has garnered significant attention in the pharmaceutical and chemical research communities. This ester derivative of piperidine is known for its unique structural features, which make it a valuable intermediate in the synthesis of various bioactive molecules. The compound's cis-3-methylpiperidine backbone and carboxylate ester functionality contribute to its versatility in medicinal chemistry and drug development.

The chemical structure of methyl cis-3-methylpiperidine-4-carboxylate includes a six-membered piperidine ring with a methyl group at the 3-position and a carboxylate ester at the 4-position. This configuration provides both lipophilic and polar characteristics, making it an excellent candidate for modifying drug solubility and bioavailability. Researchers often explore its potential in creating piperidine-based pharmaceuticals, particularly in central nervous system (CNS) targeting agents and enzyme inhibitors.

One of the most frequently asked questions about methyl cis-3-methylpiperidine-4-carboxylate is its role in modern drug discovery. With the growing demand for novel therapeutic agents, this compound serves as a critical building block for developing small-molecule drugs. Its structural flexibility allows for modifications that can enhance binding affinity to biological targets, a key consideration in designing next-generation medications. Recent studies have highlighted its utility in creating analogs for neurological and metabolic disorders.

In addition to pharmaceutical applications, methyl cis-3-methylpiperidine-4-carboxylate is also used in agrochemical research. Its piperidine core is a common motif in pesticides and herbicides, where it contributes to the stability and efficacy of active ingredients. The compound's ability to act as a chiral auxiliary in asymmetric synthesis further broadens its industrial relevance, particularly in producing enantiomerically pure agrochemicals.

The synthesis of methyl cis-3-methylpiperidine-4-carboxylate typically involves multi-step organic reactions, including esterification and ring formation. Advanced techniques such as catalytic hydrogenation and stereoselective synthesis are often employed to achieve high yields and purity. These methods align with the increasing focus on green chemistry and sustainable production practices, which are hot topics in the chemical industry today.

Market trends indicate a rising demand for piperidine derivatives, driven by their expanding applications in drug development and specialty chemicals. Methyl cis-3-methylpiperidine-4-carboxylate is no exception, with suppliers reporting growing interest from research institutions and pharmaceutical companies. The compound's compatibility with high-throughput screening and combinatorial chemistry makes it particularly appealing for modern drug discovery platforms.

From a regulatory perspective, methyl cis-3-methylpiperidine-4-carboxylate is generally regarded as safe for research purposes when handled according to standard laboratory protocols. However, researchers are advised to consult material safety data sheets (MSDS) for specific handling and storage guidelines. The compound's stability under normal conditions and its compatibility with common organic solvents further enhance its practicality in laboratory settings.

Looking ahead, the future of methyl cis-3-methylpiperidine-4-carboxylate appears promising, with potential applications emerging in material science and nanotechnology. Its molecular framework could be adapted for creating novel polymers or supramolecular assemblies, areas that are currently receiving substantial research funding. As the boundaries between chemistry, biology, and materials science continue to blur, this versatile compound is well-positioned to play a significant role in interdisciplinary innovations.

For researchers seeking high-quality methyl cis-3-methylpiperidine-4-carboxylate, it's essential to source the compound from reputable suppliers who can provide comprehensive analytical data, including NMR and HPLC purity reports. The growing emphasis on reproducibility in scientific research makes reliable sourcing and characterization of such intermediates more critical than ever before in both academic and industrial settings.

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