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    CAS 2564-83-2

    BUILDING BLOCK

    PharmaCompass
    Xls

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    2D Structure
    Also known as: 2564-83-2, 2,2,6,6-tetramethyl-1-piperidinyloxy, 2,2,6,6-tetramethylpiperidoxyl, 2,2,6,6-tetramethylpiperidine 1-oxyl, 2,2,6,6-tetramethylpiperidinyloxy, Vqn7359icq
    Molecular Formula
    C9H18NO
    Molecular Weight
    156.25  g/mol
    InChI Key
    QYTDEUPAUMOIOP-UHFFFAOYSA-N
    FDA UNII
    VQN7359ICQ
    1 2D Structure

    2D Structure

    2 Identification
    2.1 Computed Descriptors
    2.1.1 InChI
    InChI=1S/C9H18NO/c1-8(2)6-5-7-9(3,4)10(8)11/h5-7H2,1-4H3
    2.1.2 InChI Key
    QYTDEUPAUMOIOP-UHFFFAOYSA-N
    2.1.3 Canonical SMILES
    CC1(CCCC(N1[O])(C)C)C
    2.2 Other Identifiers
    2.2.1 UNII
    VQN7359ICQ
    2.3 Synonyms
    2.3.1 MeSH Synonyms

    1. 2,2,6,6-tetramethyl-1-piperidinyloxyl

    2. 2,2,6,6-tetramethyl-4-piperidine-n-oxide

    3. 2,2,6,6-tetramethylpiperidine-1-oxyl

    4. Oxoammonium Tpo

    2.3.2 Depositor-Supplied Synonyms

    1. 2564-83-2

    2. 2,2,6,6-tetramethyl-1-piperidinyloxy

    3. 2,2,6,6-tetramethylpiperidoxyl

    4. 2,2,6,6-tetramethylpiperidine 1-oxyl

    5. 2,2,6,6-tetramethylpiperidinyloxy

    6. Vqn7359icq

    7. (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl

    8. Chebi:32849

    9. Piperidinooxy, 2,2,6,6-tetramethyl-

    10. 2,2,6,6-tetramethyl Piperidine-n-oxyl

    11. 2,2,6,6-tetramethylpiperidinyl-1-oxide

    12. Tanane

    13. (2,2,6,6-tetramethylpiperidin-1-yl)oxyl

    14. 1-piperidinyloxy, 2,2,6,6-tetramethyl- (9ci)

    15. 2,2,6,6-tetramethylpiperidine 1-oxyl Free Radical

    16. Tanan

    17. Tetramethylpiperidinooxy

    18. 2,2,6,6-tetramethylpiperidine-1-oxyl Free Radical, 98%

    19. Tetramethylpiperidine Nitroxide

    20. 2,2,6,6-tetramethylpiperidinooxyl

    21. Einecs 219-888-8

    22. Tempo, Free Radical

    23. Mfcd00009599

    24. Brn 1422418

    25. Tempo [mi]

    26. Unii-vqn7359icq

    27. Ccris 8316

    28. Chembl606971

    29. Tempo, 98%

    30. Dtxsid2073300

    31. Amy23375

    32. Akos015902714

    33. Tempo, Purified By Sublimation, 99%

    34. Ccg-207968

    35. Cs-w001187

    36. Hy-w001187

    37. 2,2,6,6-tetramethyl-1-oxylpiperidine

    38. 2,2,6,6-tetramethylpiperidine-1-yloxy

    39. 2,2,6,6-tetramethylpiperindyl-1-oxide

    40. 2,2,6,6-tetramethylpiperidinooxy Radical

    41. Bp-20268

    42. 1,1,5,5-tetramethylpentamethylene Nitroxide

    43. Ft-0609130

    44. T1560

    45. En300-125971

    46. Z-1024

    47. 1-piperidinyloxy,2,2,6,6-tetramethyl-,

    48. A817947

    49. 1-$l^{1}-oxidanyl-2,2,6,6-tetramethylpiperidine

    50. 1-oxy-2,2,6,6-tetramethylpiperidine, Free Radical

    51. 2,2,6,6-tetramethylpentamethylene Nitroxide

    52. 1-$l^{1}-oxidanyl-2,2,6,6-tetramethyl-piperidine

    53. Z1255386734

    54. 4-hydroxy-2,2,6,6-tetramethylpiperidine-1-oxyl-

    55. 2,2,6,6-tetramethylpiperidine 1-oxyl, Free Radical - Solid Melt

    56. 125012-91-1

    57. 126517-51-9

    58. 25657-03-8

    59. 26933-82-4

    2.4 Create Date
    2004-09-16
    3 Chemical and Physical Properties
    Molecular Weight 156.25 g/mol
    Molecular Formula C9H18NO
    XLogP31.4
    Hydrogen Bond Donor Count0
    Hydrogen Bond Acceptor Count1
    Rotatable Bond Count0
    Exact Mass g/mol
    Monoisotopic Mass g/mol
    Topological Polar Surface Area4.2
    Heavy Atom Count11
    Formal Charge0
    Complexity136
    Isotope Atom Count0
    Defined Atom Stereocenter Count0
    Undefined Atom Stereocenter Count0
    Defined Bond Stereocenter Count0
    Undefined Bond Stereocenter Count0
    Covalently Bonded Unit Count1
    4 Pharmacology and Biochemistry
    4.1 MeSH Pharmacological Classification

    Antioxidants

    Naturally occurring or synthetic substances that inhibit or retard oxidation reactions. They counteract the damaging effects of oxidation in animal tissues. (See all compounds classified as Antioxidants.)