Structure

1,4-Piperidinedicarboxylicacid,4-(2-propen-1-yl)-,1-(1,1-dimethylethyl)4-ethyl ester

CAS
146603-99-8
Catalog Number
ACM146603998
Category
Other Products
Molecular Weight
297.389880 [g/mol]
Molecular Formula
C16H27NO4

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Specification

Synonyms
146603-99-8, Ethyl 1-Boc-4-allyl-4-piperidinecarboxylate, Ethyl N-Boc-4-allylpiperidine-4-carboxylate, 1-tert-butyl 4-ethyl 4-allylpiperidine-1,4-dicarboxylate, PubChem21097, SureCN1281827, 673730_ALDRICH, AKOS015912171, RL01847, AK-79992, KB-13310, AB1001340, KB-251966, I14-35885, 1-tert-butyl-4-ethyl-4-allylpiperidine-1,4-dicarboxylate, Ethyl 4-allyl-1-(tert-butoxycarbonyl)piperidine-4-carboxylate, 1-(1,1-Dimethylethyl) 4-ethyl 4-(2-propenyl)-1,4-piperidinedicarboxylate, 1,4-Piperidinedicarboxylicacid, 4-(2-propen-1-yl)-, 1-(1,1-dimethylethyl) 4-ethyl ester
IUPAC Name
1-O-tert-butyl 4-O-ethyl 4-prop-2-enylpiperidine-1,4-dicarboxylate
SMILES
CCOC(=O)C1(CCN(CC1)C(=O)OC(C)(C)C)CC=C
InChI Key
FOOVEGXEARQUBR-UHFFFAOYSA-N
Boiling Point
392.5ºC at 760 mmHg
Flash Point
191.2ºC
Density
1.257g/cm³
Exact Mass
297.19400
H-Bond Acceptor
4
H-Bond Donor
0

Upstream Synthesis Route 1

  • 106-95-6
  • 142851-03-4
  • 146603-99-8

Reference: [1]Current Patent Assignee: MERCK & CO INC - US2003/225059, 2003, A1
Location in patent: Page 27

Downstream Synthesis Route 1

  • 146603-99-8
  • 4427-25-2

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 13, p. 1759 - 1762

Downstream Synthesis Route 2

  • 146603-99-8
  • 374794-96-4

Reference: [1] Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 13, p. 1759 - 1762

Downstream Synthesis Route 3

  • 146603-99-8
  • 236406-39-6

Reference: [1] Patent: WO2016/42452, 2016, A1,

Downstream Synthesis Route 4

  • 146603-99-8
  • 247133-32-0

Reference: [1]Cooper, Laura C.; Carlson, Emma J.; Castro, Jose L.; Chicchi, Gary G.; Dinnell, Kevin; Di Salvo, Jerry; Elliott, Jason M.; Hollingworth, Gregory J.; Kurtz, Marc M.; Ridgill, Mark P.; Rycroft, Wayne; Tsao, Kwei-Lan; Swain, Christopher J.
[Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 13, p. 1759 - 1762]

Downstream Synthesis Route 5

  • 146603-99-8
  • 4427-25-2

Reference: [1]Cooper, Laura C.; Carlson, Emma J.; Castro, Jose L.; Chicchi, Gary G.; Dinnell, Kevin; Di Salvo, Jerry; Elliott, Jason M.; Hollingworth, Gregory J.; Kurtz, Marc M.; Ridgill, Mark P.; Rycroft, Wayne; Tsao, Kwei-Lan; Swain, Christopher J.
[Bioorganic and Medicinal Chemistry Letters, 2002, vol. 12, # 13, p. 1759 - 1762]

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

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