Cas no 78345-63-8 (N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine)

N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine is a versatile amine derivative featuring a tetrahydro-2H-pyranylmethyl moiety, which enhances its stability and reactivity in synthetic applications. This compound is particularly useful as an intermediate in organic synthesis, offering a balance between nucleophilicity and steric hindrance due to its cyclic ether and amine functionalities. Its structural properties make it suitable for use in pharmaceutical and agrochemical research, where selective functionalization is required. The tetrahydro-2H-pyran group also contributes to improved solubility in common organic solvents, facilitating its handling in multi-step reactions. This compound is valued for its potential in constructing complex molecular architectures.
N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine structure
78345-63-8 structure
Product Name:N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine
CAS No:78345-63-8
MF:C8H17NO
MW:143.226682424545
CID:1085172
PubChem ID:13288216
Update Time:2025-10-31

N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine Chemical and Physical Properties

Names and Identifiers

    • N-((Tetrahydro-2H-pyran-2-yl)methyl)ethanamine
    • N-(oxan-2-ylmethyl)ethanamine
    • AG-H-14467
    • AGN-PC-00LVTZ
    • Ambcb4015227
    • CTK5E5714
    • MolPort-003-179-013
    • N-(TETRAHYDRO-2H-PYRAN-2-YLMETHYL)ETHANAMINE
    • 78345-63-8
    • N-[(Oxan-2-yl)methyl]ethanamine
    • CHEMBRDG-BB 4015227
    • SCHEMBL11060437
    • N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine
    • N-ethyl-N-(2-tetrahydropyranylmethyl)amine
    • AKOS009062378
    • DTXSID80534873
    • NWPMUJHTBUOZQN-UHFFFAOYSA-N
    • DB-188534
    • MDL: MFCD08059964
    • Inchi: 1S/C8H17NO/c1-2-9-7-8-5-3-4-6-10-8/h8-9H,2-7H2,1H3
    • InChI Key: NWPMUJHTBUOZQN-UHFFFAOYSA-N
    • SMILES: O1CCCCC1CNCC

Computed Properties

  • Exact Mass: 143.13100
  • Monoisotopic Mass: 143.131014166g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 85.3
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.9
  • Topological Polar Surface Area: 21.3?2

Experimental Properties

  • Density: 0.892
  • Boiling Point: 201.1°C at 760 mmHg
  • Flash Point: 76.6°C
  • Refractive Index: 1.439
  • PSA: 21.26000
  • LogP: 1.55590

N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine Security Information

N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
N180840-500mg
N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine
78345-63-8
500mg
$ 500.00 2022-06-03
TRC
N180840-1000mg
N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine
78345-63-8
1g
$ 830.00 2022-06-03
TRC
N180840-2500mg
N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine
78345-63-8
2500mg
$ 1655.00 2022-06-03

Additional information on N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine

Professional Introduction to N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine (CAS No. 78345-63-8)

N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine, identified by the CAS number 78345-63-8, is a significant compound in the realm of pharmaceutical chemistry and bioorganic synthesis. This molecule has garnered attention due to its unique structural features and potential applications in drug development, particularly in the design of novel bioactive molecules. The presence of a tetrahydro-2H-pyran moiety in its structure imparts distinct stereochemical and electronic properties, making it a valuable scaffold for medicinal chemists.

The compound's structure, characterized by a saturated six-membered heterocyclic ring connected to an amine group, suggests potential interactions with biological targets. Such structural motifs are frequently explored in the quest for new therapeutic agents, as they can mimic natural products or serve as privileged scaffolds that enhance binding affinity and selectivity. The 1-ethanamine portion of the molecule further contributes to its versatility, allowing for further functionalization and derivatization to tailor its pharmacological properties.

In recent years, there has been a surge in research focused on exploiting natural product-inspired scaffolds for drug discovery. The tetrahydro-2H-pyran core is particularly noteworthy, as it is found in several bioactive compounds isolated from plants and microorganisms. These natural products have served as inspiration for synthetic chemists, leading to the development of libraries of derivatives with enhanced pharmacological profiles. N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine represents a synthetic equivalent of such natural motifs, offering a platform for further exploration.

The compound's potential lies not only in its structural features but also in its reactivity. The amine group can participate in various chemical transformations, including nucleophilic additions, condensations, and couplings, which are fundamental to medicinal chemistry. This reactivity allows for the facile introduction of additional functional groups, enabling the synthesis of complex molecules with tailored biological activities. Such versatility is crucial in the early stages of drug discovery, where rapid iteration and optimization are key.

Recent advancements in computational chemistry have further enhanced the utility of compounds like N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine. Molecular modeling techniques can predict how such molecules might interact with biological targets at the atomic level. By integrating these predictions with experimental data, researchers can accelerate the design process and prioritize promising candidates for further investigation. This interdisciplinary approach has been instrumental in identifying novel therapeutic agents that might otherwise remain undiscovered.

The synthesis of N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine also highlights the importance of green chemistry principles in modern pharmaceutical research. Efficient synthetic routes that minimize waste and utilize sustainable methodologies are increasingly preferred. Recent developments in catalytic processes have enabled more streamlined syntheses of complex molecules like this one, reducing the environmental impact while maintaining high yields and purity. Such innovations align with global efforts to promote sustainable practices across all scientific disciplines.

In conclusion, N-(Tetrahydro-2H-pyran-2-ylmethyl)-1-ethanamine (CAS No. 78345-63-8) is a versatile and promising compound with significant potential in pharmaceutical research. Its unique structural features, combined with its reactivity and synthetic accessibility, make it an attractive scaffold for drug discovery efforts. As computational methods continue to evolve and green chemistry principles gain prominence, compounds like this one will play an increasingly important role in the development of new therapeutic agents that meet both scientific and environmental challenges.

Recommended suppliers
SHOCHEM(SHANGHAI) CO.,lTD
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
SHOCHEM(SHANGHAI) CO.,lTD
Suzhou Genelee Bio-Technology Co., Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Suzhou Genelee Bio-Technology Co., Ltd.
Jiangsu Xinsu New Materials Co., Ltd
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jiangsu Xinsu New Materials Co., Ltd
Jinan Hanyu Chemical Co.,Ltd.
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Bulk
Jinan Hanyu Chemical Co.,Ltd.
上海嶸奧生物技術(shù)有限公司
Gold Member
Audited Supplier Audited Supplier
CN Supplier
Reagent
上海嶸奧生物技術(shù)有限公司