Structure

Ethyl(3R)-piperidine-3-carboxylate

CAS
25137-01-3
Catalog Number
ACM25137013
Category
Other Products
Molecular Weight
157.21
Molecular Formula
C8H15NO2

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Specification

Synonyms
25137-01-3
IUPAC Name
ethyl (3R)-piperidine-3-carboxylate
SMILES
CCOC(=O)C1CCCNC1
InChI Key
XIWBSOUNZWSFKU-SSDOTTSWSA-N
Boiling Point
110ºC / 20mmHg
Flash Point
90ºC
Density
1.02 g/cm³
Appearance
Light yellow liquid
EC Number
607-565-8
Exact Mass
157.11000
Hazard Statements
Xi
H-Bond Acceptor
3
H-Bond Donor
1
Safety Description
26-36/37/39-39-36

Upstream Synthesis Route 1

  • 71962-74-8
  • 25137-01-3
  • 37675-18-6

Reference: [1] Tetrahedron Letters, 2004, vol. 45, # 13, p. 2843 - 2845
[2] Heterocycles, 1999, vol. 51, # 8, p. 1913 - 1919
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 10, p. 2829 - 2834
[4] Journal of Labelled Compounds and Radiopharmaceuticals, 2010, vol. 53, # 9, p. 598 - 600

Upstream Synthesis Route 2

  • 71962-74-8
  • 25137-01-3

Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1951, vol. 70, p. 899,913
[2] Chemische Berichte, 1969, vol. 102, p. 2864
[3] Gazzetta Chimica Italiana, 1972, vol. 102, p. 189,190, 192, 193
[4] Bulletin des Societes Chimiques Belges, 1995, vol. 104, # 12, p. 721 - 726
[5] Organic Process Research and Development, 2003, vol. 7, # 6, p. 866 - 872

Upstream Synthesis Route 3

  • 614-18-6
  • 25137-01-3

Reference: [1] Recueil des Travaux Chimiques des Pays-Bas, 1951, vol. 70, p. 899,913

Upstream Synthesis Route 4

  • 71962-74-8
  • 25137-01-3
  • 37675-18-6

Reference: [1]Tetrahedron Letters,2004,vol. 45,p. 2843 - 2845
[2]Heterocycles,1999,vol. 51,p. 1913 - 1919
[3]Bioorganic and Medicinal Chemistry Letters,2009,vol. 19,p. 2829 - 2834
[4]Journal of labelled compounds and radiopharmaceuticals,2010,vol. 53,p. 598 - 600

Downstream Synthesis Route 1

  • 25137-01-3
  • 498-95-3

Reference: [1]Recueil des Travaux Chimiques des Pays-Bas,1951,vol. 70,p. 899,913

Downstream Synthesis Route 2

  • 25137-01-3
  • 37675-20-0

Reference: [1]Journal of Organic Chemistry,1991,vol. 56,p. 1166 - 1170
[2]Tetrahedron Letters,2002,vol. 43,p. 8917 - 8919
[3]Chemical and Pharmaceutical Bulletin,2005,vol. 53,p. 437 - 440
[4]Patent: EP1553074,2005,A1 .Location in patent: Page/Page column 37

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

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