Structure

1-Trifluoroacetyl piperidine

CAS
340-07-8
Catalog Number
ACM340078
Category
Other Products
Molecular Weight
181.1556096
Molecular Formula
C7H10F3NO

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Specification

Synonyms
1-Trifluoroacetyl piperidine, 683035_ALDRICH, 340-07-8
IUPAC Name
2,2,2-trifluoro-1-piperidin-1-ylethanone
SMILES
C1CCN(CC1)C(=O)C(F)(F)F
InChI Key
BCJUMGSHTLYECD-UHFFFAOYSA-N
Boiling Point
247.5ºC at 760 mmHg
Flash Point
77ºC
Density
1.226 g/mL at 25ºC
Appearance
light yellow oil
Exact Mass
181.07100
Hazard Statements
T: Toxic;
H-Bond Acceptor
4
H-Bond Donor
0
Safety Description
45-61

Upstream Synthesis Route 1

  • 110-89-4
  • 383-63-1
  • 340-07-8

Reference: [1]Sammelsont, Robert E.; Casida, John E.
[Journal of Organic Chemistry, 2003, vol. 68, # 21, p. 8075 - 8079]
[2]Current Patent Assignee: THE KALYANI GROUP - WO2021/240331, 2021, A1
Location in patent: Page/Page column 8
[3]Laduron, Frederic; Nyns, Claire; Janousek, Zdenek; Viehe, Heinz G.
[Advanced Synthesis and Catalysis, 1997, vol. 339, # 8, p. 697 - 707]
[4]Gómez, Antonio Bermejo; Cortés González, Miguel A.; Lübcke, Marvin; Johansson, Magnus J.; Halldin, Christer; Szabó, Kálmán J.; Schou, Magnus
[Chemical Communications, 2016, vol. 52, # 97, p. 13963 - 13966]
[5]Joullie
[Journal of the American Chemical Society, 1955, vol. 77, p. 6662]

Upstream Synthesis Route 2

  • 110-89-4
  • 407-25-0
  • 340-07-8

Reference: [1]Schenck, Hilary A.; Lenkowski, Paul W.; Choudhury-Mukherjee, Indrani; Ko, Seong-Hoon; Stables, James P.; Patel, Manoj K.; Brown, Milton L.
[Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 5, p. 979 - 993]

Downstream Synthesis Route 1

  • 340-07-8
  • 38480-28-3
  • 2557-70-2

Reference: [1] Angewandte Chemie - International Edition, 2013, vol. 52, # 52, p. 14191 - 14195[2] Angew. Chem., 2013, vol. 125, # 52, p. 14441 - 14445,5

Downstream Synthesis Route 2

  • 340-07-8
  • 591-17-3
  • 1736-06-7

Reference: [1] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 5, p. 979 - 993
[2] Angewandte Chemie - International Edition, 2013, vol. 52, # 52, p. 14191 - 14195[3] Angew. Chem., 2013, vol. 125, # 52, p. 14441 - 14445,5

Downstream Synthesis Route 3

  • 340-07-8
  • 108-37-2
  • 321-31-3

Reference: [1] Bioorganic and Medicinal Chemistry, 2004, vol. 12, # 5, p. 979 - 993

* For details of the synthesis route, please refer to the original source to ensure accuracy.

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