Cas no 5064-46-0 ([(oxolan-2-yl)methyl](propan-2-yl)amine)

Technical Introduction: [(Oxolan-2-yl)methyl](propan-2-yl)amine is a tertiary amine featuring a tetrahydrofuran (oxolane) moiety and an isopropyl group. This compound exhibits versatility as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical applications. Its structure combines the reactivity of an amine with the stability and solvation properties imparted by the oxolane ring, making it useful in nucleophilic substitutions and catalyst systems. The isopropyl group enhances steric control, potentially improving selectivity in synthetic pathways. The compound’s balanced lipophilicity and polarity may also contribute to favorable solubility profiles in various reaction media. Suitable for controlled functionalization, it serves as a valuable building block in specialty chemical development.
[(oxolan-2-yl)methyl](propan-2-yl)amine structure
5064-46-0 structure
Product Name:[(oxolan-2-yl)methyl](propan-2-yl)amine
CAS No:5064-46-0
MF:C8H17NO
MW:143.226682424545
CID:383531
PubChem ID:263171
Update Time:2025-11-05

[(oxolan-2-yl)methyl](propan-2-yl)amine Chemical and Physical Properties

Names and Identifiers

    • 2-Furanmethanamine,tetrahydro-N-(1-methylethyl)-
    • ISOPROPYL-(TETRAHYDRO-FURAN-2-YLMETHYL)-AMINE
    • 1-isopropyl-2-methylacetylene
    • 2-methyl-4-pentyne
    • 2-Pentyne, 4-methyl-
    • 4-Methyl-2-pentyne
    • 649082_ALDRICH
    • AC1L3HPH
    • ACMC-1CO71
    • ANW-24313
    • CTK1A7541
    • isopropyl(methyl)acetylene
    • iso-propylmethylacetylene
    • Isopropylmethylacetylene
    • isopropyl-tetrahydrofurfuryl-amine
    • methylisopropylacetylene
    • N-Isopropyl-tetrahydrofurfurylamin
    • [(oxolan-2-yl)methyl](propan-2-yl)amine
    • isopropyl-(tetrahydro-furan-2-ylmethyl)-amine, AldrichCPR
    • (oxolan-2-ylmethyl)(propan-2-yl)amine
    • AKOS000156980
    • HMS1704A18
    • SCHEMBL105301
    • AKOS017281370
    • N-(oxolan-2-ylmethyl)propan-2-amine
    • EN300-162775
    • NSC97525
    • Tetrahydro-N-(1-methylethyl)-2-furanmethanamine
    • N-((Tetrahydrofuran-2-yl)methyl)propan-2-amine
    • PELLLKANMONICH-UHFFFAOYSA-N
    • 5064-46-0
    • CS-0235847
    • NSC-97525
    • 2-Propenamide, N-[(2-methoxyphenyl)methyl]-
    • isopropyl(oxolan-2-ylmethyl)amine
    • DB-087260
    • MDL: MFCD03856628
    • Inchi: 1S/C8H17NO/c1-7(2)9-6-8-4-3-5-10-8/h7-9H,3-6H2,1-2H3
    • InChI Key: PELLLKANMONICH-UHFFFAOYSA-N
    • SMILES: O1CCCC1CNC(C)C

Computed Properties

  • Exact Mass: 143.13111
  • Monoisotopic Mass: 143.131
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 3
  • Complexity: 93.3
  • 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: 1
  • Topological Polar Surface Area: 21.3?2

Experimental Properties

  • Density: 0.897
  • Boiling Point: 192.3°Cat760mmHg
  • Flash Point: 73.1°C
  • Refractive Index: 1.441
  • PSA: 21.26

[(oxolan-2-yl)methyl](propan-2-yl)amine Security Information

  • Hazard Category Code: 22
  • Hazardous Material Identification: Xi Xn
  • HazardClass:IRRITANT

[(oxolan-2-yl)methyl](propan-2-yl)amine Pricemore >>

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Additional information on [(oxolan-2-yl)methyl](propan-2-yl)amine

[(oxolan-2-yl)methyl](propan-2-yl)amine - A Comprehensive Overview

The compound [(oxolan-2-yl)methyl](propan-2-yl)amine, also known by its CAS number 5064-46-0, is a versatile organic compound with a wide range of applications in various industries. This compound is a derivative of propan-2-ylamine, where the amine group is substituted with an oxolan-2-ylmethyl group. The structure of this compound can be represented as (CH3)2NCH2C5H9O, where the oxolane ring (a five-membered cyclic ether) introduces unique chemical properties and reactivity.

[(oxolan-2-yl)methyl](propan-2-yl)amine has gained significant attention in recent years due to its role in the synthesis of advanced materials and pharmaceuticals. Its ability to act as a chelating agent and its compatibility with various organic reactions make it an essential intermediate in many chemical processes. Recent studies have highlighted its potential in the development of biodegradable polymers and drug delivery systems, where its amphiphilic nature plays a crucial role.

One of the most notable applications of [(oxolan-2-yl)methyl](propan-2-yl)amine is in the field of catalysis. Researchers have demonstrated that this compound can serve as an effective ligand for transition metal catalysts, enhancing their activity and selectivity in reactions such as olefin polymerization and cross-coupling reactions. This has opened new avenues for sustainable chemical manufacturing processes, aligning with the growing demand for eco-friendly technologies.

In addition to its catalytic applications, [(oxolan-2-yl)methyl](propan-2-yl)amine has been explored for its potential in the synthesis of antiviral agents. Recent findings suggest that this compound can inhibit certain viral enzymes, making it a promising candidate for antiviral drug development. Its ability to interact with viral proteins through hydrogen bonding and hydrophobic interactions has been extensively studied, paving the way for novel therapeutic strategies.

The synthesis of [(oxolan-2-yl)methyl](propan-2-yllamine) typically involves a two-step process: first, the preparation of the oxolane ring through ring-opening polymerization or other cyclization techniques, followed by nucleophilic substitution to introduce the amine group. This process ensures high purity and structural integrity, which are critical for its performance in downstream applications.

From an environmental perspective, [(oxolan-yllmethyl](propan-yllamine) exhibits favorable biodegradation properties, making it suitable for use in environmentally friendly products. Its ability to degrade under aerobic conditions without releasing harmful byproducts aligns with global efforts to reduce chemical waste and promote sustainability.

In conclusion, [(oxolan-yllmethyl](propan-yllamine) (CAS No. 5064-y6-y) is a multifaceted compound with diverse applications across various industries. Its unique chemical properties, combined with recent advancements in research, position it as a key player in the development of innovative materials and therapeutic agents. As ongoing studies continue to uncover new potentials for this compound, its significance in the chemical landscape is expected to grow further.

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