Structure

1-Piperazinecarboxylicacid,4-(5-amino-2-pyridinyl)-,1,1-dimethylethyl ester

CAS
119285-07-3
Catalog Number
ACM119285073
Category
Other Products
Molecular Weight
278.35
Molecular Formula
C14H22N4O2

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  • Product Description
  • Case Study
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  • Custom Q&A
  • Synthetic Use
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Specification

Synonyms
119285-07-3, 1-Boc-4-(5-Aminopyridin-2-yl)piperazine, tert-butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate, 1-Piperazinecarboxylicacid, 4-(5-amino-2-pyridinyl)-, 1,1-dimethylethyl ester, SureCN265889, ACMC-1C23V, AGN-PC-01NP48, CTK4B1210, MolPort-000-001-350, ANW-52199, AKOS005071527, AG-D-42096, MCULE-4719625718, RP15397, aminopyridinyltetrahydropyrazinecarboxylate, AK-18107, BR-18107, EN001981, KB-34566, AM20070218
IUPAC Name
tert-butyl 4-(5-aminopyridin-2-yl)piperazine-1-carboxylate
SMILES
CC(C)(C)OC(=O)N1CCN(CC1)C2=NC=C(C=C2)N
InChI Key
RMHRRMBFHGEDSR-UHFFFAOYSA-N
Boiling Point
470.4ºC at 760mmHg
Melting Point
98-101ºC
Flash Point
238.3ºC
Density
1.182g/cm³
Exact Mass
278.17400
Hazard Statements
Xi: Irritant;
H-Bond Acceptor
5
H-Bond Donor
1

Upstream Synthesis Route 1

  • 193902-78-2
  • 119285-07-3

Reference: [1] Patent: US2005/182078, 2005, A1, . Location in patent: Page/Page column 9; 12

Upstream Synthesis Route 2

  • 57260-71-6
  • 119285-07-3

Reference: [1] Journal of Medicinal Chemistry, 2011, vol. 54, # 7, p. 2433 - 2446
[2] Tetrahedron Letters, 2011, vol. 52, # 45, p. 5905 - 5909
[3] Chinese Chemical Letters, 2013, vol. 24, # 4, p. 303 - 306
[4] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 23, p. 6410 - 6414
[5] Patent: EP2773638, 2015, B1,

Upstream Synthesis Route 3

  • 4548-45-2
  • 119285-07-3

Reference: [1] Journal of Medicinal Chemistry, 2011, vol. 54, # 7, p. 2433 - 2446
[2] Bioorganic and Medicinal Chemistry Letters, 2011, vol. 21, # 16, p. 4779 - 4783
[3] Chinese Chemical Letters, 2013, vol. 24, # 4, p. 303 - 306
[4] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 23, p. 6410 - 6414

Downstream Synthesis Route 1

  • 501-53-1
  • 119285-07-3
  • 510729-40-5

Reference: [1]Patent: WO2004/9587,2004,A1 .Location in patent: Page 37

Downstream Synthesis Route 2

  • 1436-34-6
  • 119285-07-3
  • 1010398-43-2

Reference: [1]Patent: WO2008/29266,2008,A1 .Location in patent: Page/Page column 30-31

Downstream Synthesis Route 3

  • 119285-07-3
  • 510729-49-4

Reference: [1]Bioorganic and Medicinal Chemistry,2003,vol. 11,p. 2313 - 2319

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

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