Cas no 1353971-24-0 ((4-Methylamino-cyclohexyl)-carbamic acid benzyl ester)

(4-Methylamino-cyclohexyl)-carbamic acid benzyl ester is a cyclohexylamine derivative featuring a benzyl ester-protected carbamate group and a methylamino substituent at the 4-position. This compound is primarily utilized as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and bioactive molecules. Its structural features, including the carbamate protection and secondary amine functionality, make it valuable for controlled amine derivatization and peptide coupling reactions. The benzyl ester group enhances solubility in organic solvents, facilitating purification and handling. The compound’s stability under standard conditions and well-defined reactivity profile contribute to its utility in medicinal chemistry and drug discovery research.
(4-Methylamino-cyclohexyl)-carbamic acid benzyl ester structure
1353971-24-0 structure
Product Name:(4-Methylamino-cyclohexyl)-carbamic acid benzyl ester
CAS No:1353971-24-0
MF:C15H22N2O2
MW:262.347383975983
CID:2155157
Update Time:2025-10-28

(4-Methylamino-cyclohexyl)-carbamic acid benzyl ester Chemical and Physical Properties

Names and Identifiers

    • (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester
    • (1R,4R)-(4-Methylamino-cyclohexyl)-carbamic acid benzyl ester
    • Benzyl (4-(methylamino)cyclohexyl)carbamate
    • AM93708
    • AM102093
    • Benzyl [trans-4-(methylamino)cyclohexyl]carbamate
    • (4-methylaminocyclohexyl)carbamic acid benzyl ester
    • (1R,4R)-(4-methylaminocyclohexyl)carbamic acid benzyl ester
    • Inchi: 1S/C15H22N2O2/c1-16-13-7-9-14(10-8-13)17-15(18)19-11-12-5-3-2-4-6-12/h2-6,13-14,16H,7-11H2,1H3,(H,17,18)
    • InChI Key: XDCBEZOARUDTIU-UHFFFAOYSA-N
    • SMILES: O(CC1C=CC=CC=1)C(NC1CCC(CC1)NC)=O

Computed Properties

  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 19
  • Rotatable Bond Count: 5
  • Complexity: 269
  • Topological Polar Surface Area: 50.4

(4-Methylamino-cyclohexyl)-carbamic acid benzyl ester Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
Fluorochem
087671-1g
4-Methylamino-cyclohexyl)-carbamic acid benzyl ester
1353971-24-0
1g
£945.00 2022-02-28

Additional information on (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester

Comprehensive Overview of (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester (CAS No. 1353971-24-0)

(4-Methylamino-cyclohexyl)-carbamic acid benzyl ester (CAS No. 1353971-24-0) is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound, often referred to as a cyclohexyl carbamate derivative, is characterized by its unique structural features, including a benzyl ester group and a methylamino-cyclohexyl moiety. Its molecular formula and precise weight make it a subject of interest for researchers exploring novel drug intermediates and bioactive molecules.

The chemical properties of (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester include its solubility in organic solvents such as dimethyl sulfoxide (DMSO) and methanol, which facilitates its use in laboratory settings. Its stability under controlled conditions makes it suitable for various synthetic applications. Researchers often investigate its reactivity and potential as a building block in the synthesis of more complex molecules, particularly in the development of central nervous system (CNS) targeting compounds.

One of the key applications of (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester lies in its role as a pharmaceutical intermediate. It is frequently utilized in the synthesis of compounds with potential therapeutic effects, such as neuromodulators or enzyme inhibitors. Recent studies have explored its utility in designing molecules that interact with specific receptors, which could lead to breakthroughs in treating neurological disorders. This aligns with the growing interest in precision medicine and targeted drug delivery systems, which are hot topics in modern pharmacology.

From a market perspective, the demand for (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester is driven by its niche applications in drug discovery and development. Pharmaceutical companies and research institutions are increasingly seeking high-purity versions of this compound to support their R&D efforts. The rise of AI-driven drug discovery platforms has further amplified interest in such specialized intermediates, as they are often used in high-throughput screening and computational modeling.

In terms of safety and handling, (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester should be stored in a cool, dry environment, away from direct sunlight. While it is not classified as a hazardous material under standard regulations, proper laboratory practices, including the use of personal protective equipment (PPE), are recommended when handling this compound. Researchers often inquire about its material safety data sheet (MSDS) and storage conditions, which are critical for ensuring safe usage.

The synthetic pathways for producing (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester typically involve multi-step organic reactions, including amination and esterification processes. Advanced techniques such as microwave-assisted synthesis and catalysis have been explored to improve yield and efficiency. These innovations are part of the broader trend toward green chemistry and sustainable manufacturing practices in the chemical industry.

Looking ahead, the potential of (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester in drug development and biochemical research remains promising. Its structural versatility and compatibility with various synthetic methodologies position it as a valuable tool for scientists. As the field of medicinal chemistry continues to evolve, compounds like this will likely play a pivotal role in discovering next-generation therapeutics.

For researchers and industry professionals seeking detailed information about (4-Methylamino-cyclohexyl)-carbamic acid benzyl ester, it is advisable to consult peer-reviewed journals, patent databases, and specialized chemical suppliers. The compound's CAS No. 1353971-24-0 serves as a unique identifier, ensuring accurate sourcing and regulatory compliance. With ongoing advancements in chemical informatics and data-driven research, access to reliable information about such compounds has become more streamlined than ever.

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