Cas no 148088-78-2 (Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester)

Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester, is a specialized organic compound with applications in pharmaceutical and chemical synthesis. Its structure features a carbamate group linked to a benzyl ester and a methylaminoethyl moiety, making it a versatile intermediate for modifying bioactive molecules. The compound's stability and reactivity allow for selective functionalization in drug development, particularly in prodrug formulations or targeted delivery systems. Its phenylmethyl ester group enhances solubility in organic solvents, facilitating purification and handling. This compound is valued for its potential in creating derivatives with tailored pharmacokinetic properties, contributing to research in medicinal chemistry and fine chemical synthesis.
Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester structure
148088-78-2 structure
Product Name:Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester
CAS No:148088-78-2
MF:C12H18N2O2
MW:222.283523082733
MDL:MFCD27979855
CID:1319529
PubChem ID:18978086
Update Time:2025-05-22

Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester Chemical and Physical Properties

Names and Identifiers

    • Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester
    • benzyl methyl(2-(methylamino)ethyl)carbamate
    • benzyl N-methyl-N-[2-(methylamino)ethyl]carbamate
    • SCHEMBL7368731
    • EN300-6948359
    • A1-48590
    • D84370
    • Carbamic acid, N-methyl-N-[2-(methylamino)ethyl]-, phenylmethyl ester
    • MFCD27979855
    • CS-0131094
    • DTXSID90597050
    • 148088-78-2
    • DA-10080
    • Benzyl methyl[2-(methylamino)ethyl]carbamate
    • AS-77583
    • MDL: MFCD27979855
    • Inchi: 1S/C12H18N2O2/c1-13-8-9-14(2)12(15)16-10-11-6-4-3-5-7-11/h3-7,13H,8-10H2,1-2H3
    • InChI Key: QTLVLLWKMZINAR-UHFFFAOYSA-N
    • SMILES: O(CC1C=CC=CC=1)C(N(C)CCNC)=O

Computed Properties

  • Exact Mass: 222.13694
  • Monoisotopic Mass: 222.136827821g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 6
  • Complexity: 203
  • 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: 1.7
  • Topological Polar Surface Area: 41.6?2

Experimental Properties

  • PSA: 41.57

Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester Pricemore >>

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Additional information on Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester

Comprehensive Overview of Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester (CAS No. 148088-78-2)

Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester (CAS No. 148088-78-2) is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound, often referred to by its systematic name, belongs to the class of carbamate esters, which are known for their versatility in medicinal chemistry and drug development. The unique structural features of this molecule, including the methylaminoethyl and phenylmethyl groups, contribute to its potential applications in targeted therapies and enzymatic studies.

In recent years, the demand for carbamate derivatives like Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester has surged due to their role in modulating biological pathways. Researchers are particularly interested in its potential as a protease inhibitor or neurotransmitter analog, aligning with current trends in precision medicine and neuroscience. The compound’s CAS No. 148088-78-2 is frequently searched in academic databases, reflecting its relevance in cutting-edge studies.

One of the most discussed topics in the context of Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester is its synthetic accessibility and structural stability. Chemists have explored its reactivity under various conditions, highlighting its compatibility with green chemistry principles—a hot topic in sustainable science. Additionally, its phenylmethyl ester moiety has been investigated for its potential to enhance bioavailability, a critical factor in drug design.

The compound’s methyl[2-(methylamino)ethyl] side chain also makes it a candidate for drug delivery systems, particularly in nanomedicine. This aligns with the growing interest in targeted drug delivery and personalized therapeutics, which dominate current pharmaceutical research. Users often search for terms like "carbamate ester applications" or "CAS 148088-78-2 uses", indicating a need for detailed, actionable insights.

From a regulatory perspective, Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester is not classified as a hazardous material, making it a safer alternative for laboratory use compared to more reactive compounds. Its low toxicity profile and high purity standards are frequently cited in supplier catalogs, addressing another common query among researchers: "Is CAS 148088-78-2 safe for lab use?".

In summary, Carbamic acid, methyl[2-(methylamino)ethyl]-, phenylmethyl ester (CAS No. 148088-78-2) represents a promising avenue for interdisciplinary research. Its structural complexity and functional diversity make it a valuable tool for advancing biomedical innovation and therapeutic development. As the scientific community continues to explore its potential, this compound is poised to remain a focal point in both academic and industrial settings.

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