Date published: 2026-4-24

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4-Aminotetrahydropyran (CAS 38041-19-9)

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Alternate Names:
Tetrahydro-2H-pyran-4-amine
CAS Number:
38041-19-9
Molecular Weight:
101.15
Molecular Formula:
C5H11NO
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4-Aminotetrahydropyran is a chemical compound that functions as a building block in organic synthesis. It serves as a key intermediate in the preparation of various agrochemicals, and other fine chemicals. Participates in a range of chemical reactions, including reductive amination, hydrogenation, and ring-opening reactions, enabling the synthesis of diverse molecular structures. At the molecular level, 4-Aminotetrahydropyran undergoes specific transformations, facilitating the formation of new chemical bonds and the creation of complex molecular architectures. Its mechanism of action involves participating in various pathways, contributing to the development of novel compounds with potential applications and development.


4-Aminotetrahydropyran (CAS 38041-19-9) References

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  2. Stereoselective one-pot, three-component synthesis of 4-amidotetrahydropyran.  |  Reddy, UC., et al. 2008. J Org Chem. 73: 1628-30. PMID: 18198890
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  5. Optimization of 5-(2,6-dichlorophenyl)-3-hydroxy-2-mercaptocyclohex-2-enones as potent inhibitors of human lactate dehydrogenase.  |  Labadie, S., et al. 2015. Bioorg Med Chem Lett. 25: 75-82. PMID: 25466195
  6. A Unified Approach to the Four Azaindoline Families by Inter-/Intramolecular Annulative Diamination of Vinylpyridines.  |  Danneman, MW., et al. 2015. Org Lett. 17: 3806-9. PMID: 26186041
  7. Two-Dimensional Layered Perovskite Ferroelectric with Giant Piezoelectric Voltage Coefficient.  |  Chen, XG., et al. 2020. J Am Chem Soc. 142: 1077-1082. PMID: 31851495
  8. Biphenylurea/thiourea derivatives tagged with heteroarylsulfonamide motifs as novel VEGFR2 inhibitors; Design, synthesis and anti-angiogenic activity.  |  Al-Ansary, GH., et al. 2021. Bioorg Chem. 107: 104640. PMID: 33485105
  9. N-Heterocyclic carbene-catalyzed deaminative cross-coupling of aldehydes with Katritzky pyridinium salts.  |  Kim, I., et al. 2020. Chem Sci. 11: 3192-3197. PMID: 34122824
  10. Development of radioiodinated pyrimidinopyridone derivatives as targeted imaging probes of activated p38α for single photon emission computed tomography.  |  Hashimoto, T., et al. 2021. Ann Nucl Med. 35: 1293-1304. PMID: 34410619
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  12. High Piezoelectric Output Voltage from Blue Fluorescent N,N-Dimethyl-4-nitroaniline Nano Crystals in Poly-L-Lactic Acid Electrospun Fibers.  |  Baptista, RMF., et al. 2022. Materials (Basel). 15: PMID: 36431444
  13. Ferroelectric hybrid organic-inorganic perovskites and their structural and functional diversity.  |  Zhang, T., et al. 2023. Natl Sci Rev. 10: nwac240. PMID: 36817836
  14. Lewis-Acid-Catalyzed Reductive Hydroalkoxylation of Propargylic N-Hydroxylamines Gives Stereoselective Access to Isoxazolidines.  |  Gharpure, SJ., et al. 2023. Org Lett. 25: 2525-2530. PMID: 37015053

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4-Aminotetrahydropyran, 1 g

sc-232404
1 g
$95.00

4-Aminotetrahydropyran, 5 g

sc-232404A
5 g
$114.00

4-Aminotetrahydropyran, 25 g

sc-232404B
25 g
$500.00