Cas no 62999-86-4 (N,N,5,5-Tetramethyl-1,3-dioxane-2-amine)

N,N,5,5-Tetramethyl-1,3-dioxane-2-amine is a cyclic amine derivative with a dioxane backbone, characterized by its tetramethyl substitution pattern. This compound is notable for its structural rigidity and steric hindrance, which can influence reactivity and stability in synthetic applications. Its amine functionality makes it a potential intermediate in the synthesis of pharmaceuticals, agrochemicals, or specialty chemicals. The dioxane ring provides enhanced solubility in organic solvents, while the tetramethyl groups may contribute to improved thermal stability. This compound is of interest for researchers exploring novel heterocyclic frameworks or seeking tailored steric and electronic properties in amine-based systems.
N,N,5,5-Tetramethyl-1,3-dioxane-2-amine structure
62999-86-4 structure
Product Name:N,N,5,5-Tetramethyl-1,3-dioxane-2-amine
CAS No:62999-86-4
MF:C8H17NO2
MW:159.2260825634
CID:883693
Update Time:2026-04-29

N,N,5,5-Tetramethyl-1,3-dioxane-2-amine Chemical and Physical Properties

Names and Identifiers

    • N,N,5,5-tetramethyl-1,3-dioxan-2-amine
    • (5,5-dimethyl-[1,3]dioxan-2-yl)-dimethyl-amine
    • 2-Dimethylamino-5,5-dimethyl-1,3-dioxan
    • 2-dimethylamino-5,5-dimethyl-1,3-dioxane
    • 5,5-Dimethyl-2-N,N-dimethylamino-1,3-dioxane
    • AC1L6S4T
    • AC1Q3WL9
    • AC1Q705P
    • AR-1K0648
    • CTK5B6990
    • NSC117332
    • OQVXZYBHZOTQHN-UHFFFAOYSA-
    • SureCN132563
    • N,N,5,5-Tetramethyl-1,3-dioxane-2-amine
    • Inchi： InChI=1S/C8H17NO2/c1-8(2)5-10-7(9(3)4)11-6-8/h7H,5-6H2,1-4H3
    • InChI Key： OQVXZYBHZOTQHN-UHFFFAOYSA-N
    • SMILES： CC1(C)COC(N(C)C)OC1

Computed Properties

  • Exact Mass: 159.12601
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 1

Experimental Properties

  • PSA: 21.7
  • LogP: 0.90460

N,N,5,5-Tetramethyl-1,3-dioxane-2-amine Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
TRC
T205675-250mg
N,N,5,5-Tetramethyl-1,3-dioxane-2-amine
 62999-86-4
250mg
 $ 50.00 2022-06-03
TRC
T205675-500mg
N,N,5,5-Tetramethyl-1,3-dioxane-2-amine
 62999-86-4
500mg
 $ 65.00 2022-06-03
TRC
T205675-2.5g
N,N,5,5-Tetramethyl-1,3-dioxane-2-amine
 62999-86-4
2.5g
 $ 135.00 2022-06-03

N,N,5,5-Tetramethyl-1,3-dioxane-2-amine Related Literature

Additional information on N,N,5,5-Tetramethyl-1,3-dioxane-2-amine

N,N,5,5-Tetramethyl-1,3-Dioxan-2-Amine: A Comprehensive Overview

N,N,5,5-tetramethyl-1,3-dioxan-2-amine is a unique organic compound that has garnered significant attention in the fields of pharmaceuticals and chemical synthesis. This compound, with its CAS Registry Number 62999-86-4, belongs to the class of dioxane derivatives, which are known for their diverse applications in drug delivery systems, synthetic chemistry, and biological research.

The structure of N,N,5,5-tetramethyl-1,3-dioxan-2-amine features a central dioxane ring with two methyl groups attached to the nitrogen atom at position 2, and two additional methyl groups at positions 5 and 5. This configuration makes it highly versatile for various chemical reactions and biological applications. Recent studies have highlighted its potential as an intermediate in the synthesis of complex molecules, including those with cancer therapeutic properties.

In the realm of pharmaceutical research, this compound has been explored for its ability to stabilize bioactive compounds during formulation. Its dioxane ring provides excellent solubility and stability, making it a valuable component in drug delivery systems such as nanoparticles or controlled-release formulations. Furthermore, the presence of the amine group enables functionalization for targeting specific biological pathways.

Recent advancements in sustainable chemistry have also positioned N,N,5,5-tetramethyl-1,3-dioxan-2-amine as a green alternative to traditional solvents and reagents. Its biodegradable nature and low environmental impact make it an attractive choice for eco-friendly chemical processes.

Emerging research in synthetic biology has identified this compound as a potential building block for constructing bio-inspired materials. Its structural flexibility allows for the creation of complex biomolecules that mimic natural systems, opening new avenues in biofabrication and tissue engineering.

Overall, N,N,5,5-tetramethyl-1,3-dioxan-2-amine stands out as a multifaceted compound with wide-ranging applications in pharmaceuticals, chemistry, and biotechnology. Its unique properties make it an invaluable tool for advancing innovative solutions in these fields.

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