Home Other Building Blocks 143900-44-1
143900-44-1,MFCD04115307
Catalog No.:AA0032DR

143900-44-1 | (S)-1-Boc-3-hydroxypiperidine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$8.00   $6.00
- +
5g
98%
in stock  
$11.00   $8.00
- +
10g
98%
in stock  
$13.00   $9.00
- +
25g
98%
in stock  
$29.00   $21.00
- +
100g
98%
in stock  
$115.00   $81.00
- +
250g
97%
in stock  
$262.00   $183.00
- +
500g
98%
in stock  
$323.00   $226.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0032DR
Chemical Name:
(S)-1-Boc-3-hydroxypiperidine
CAS Number:
143900-44-1
Molecular Formula:
C10H19NO3
Molecular Weight:
201.2628
MDL Number:
MFCD04115307
SMILES:
O[C@H]1CCCN(C1)C(=O)OC(C)(C)C
Properties
Properties
 
Form:
Solid  
MP:
34-40 °C  
Solubility:
Soluble in methanol.  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
210  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
2  
XLogP3:
1  

Upstream Synthesis Route

[1]Patent:WO2014/188173,2014,A1,.Locationinpatent:Paragraph00224

[2]Patent:CN105399756,2016,A,.Locationinpatent:Paragraph0152;0167-0168

[3]MedChemComm,2014,vol.5,#12,p.1879-1886

[4]Patent:WO2017/134684,2017,A2,.Locationinpatent:Page/Pagecolumn12

[5]Patent:CN103864673,2016,B,.Locationinpatent:Paragraph0084;0085

[6]Patent:WO2017/12576,2017,A1,.Locationinpatent:Page/Pagecolumn183

[7]Patent:WO2008/109613,2008,A1,.Locationinpatent:Page/Pagecolumn217-218

[8]SyntheticCommunications,2008,vol.38,#4,p.517-524

[9]BioorganicandMedicinalChemistryLetters,2008,vol.18,#6,p.2215-2221

[10]Patent:EP2947086,2015,A1,.Locationinpatent:Paragraph0228

[11]Patent:WO2016/79693,2016,A1,.Locationinpatent:Page/Pagecolumn25

[12]Patent:CN105315283,2016,A,.Locationinpatent:Paragraph0105;0112;0113;0114

[13]Patent:WO2016/170545,2016,A1,.Locationinpatent:Page/Pagecolumn32;33

[14]Patent:WO2016/151438,2016,A1,.Locationinpatent:Page/Pagecolumn11

[15]Patent:US2017/44166,2017,A1,.Locationinpatent:Paragraph0187

[16]Patent:US2017/217970,2017,A1,.Locationinpatent:Paragraph0335

[17]Patent:WO2017/137446,2017,A1,.Locationinpatent:Page/Pagecolumn17;18;20;21

[18]Patent:US9782412,2017,B2,.Locationinpatent:Page/Pagecolumn40

[1]Patent:WO2016/210165,2016,A1,.Locationinpatent:Page/Pagecolumn76

[1]Patent:CN103864673,2016,B,

[1]Patent:CN106995446,2017,A,.Locationinpatent:Paragraph0044-0046

[2]Patent:CN106967071,2017,A,.Locationinpatent:Paragraph0019

[3]Patent:US2008/214501,2008,A1,.Locationinpatent:Page/Pagecolumn12

[4]OrganicandBiomolecularChemistry,2015,vol.13,#18,p.5147-5157

[5]Patent:WO2014/22390,2014,A1,.Locationinpatent:Paragraph95;98

[6]JournalofMedicinalChemistry,2015,vol.58,#24,p.9625-9638

[7]Patent:CN105481862,2016,A,.Locationinpatent:Paragraph0166;0167;0170

[8]Patent:WO2017/163257,2017,A1,.Locationinpatent:Page/Pagecolumn19

[9]Patent:CN106008526,2016,A,.Locationinpatent:Paragraph0016;0063;0064;0065

[10]Patent:CN107759602,2018,A,.Locationinpatent:Paragraph0231;0236-0237

[1]Patent:WO2013/191965,2013,A1,

[2]Patent:WO2014/22569,2014,A1,

[3]Patent:US8673925,2014,B1,

[4]Patent:WO2016/170545,2016,A1,

[5]Patent:WO2016/151438,2016,A1,

[6]Patent:WO2016/151438,2016,A1,

[7]Patent:CN105399756,2016,A,

[8]Patent:CN106146511,2016,A,

[9]Patent:WO2017/137446,2017,A1,

Downstream Synthesis Route

[1]Patent:WO2005/26152,2005,A1.Locationinpatent:Page/Pagecolumn132

[2]Patent:WO2017/137446,2017,A1.Locationinpatent:Page/Pagecolumn17;20

[3]Tetrahedron,2007,vol.63,p.331-336

[1]Patent:WO2014/188173,2014,A1.Locationinpatent:Paragraph00224

[2]Patent:CN105399756,2016,A.Locationinpatent:Paragraph0152;0167-0168

[3]MedChemComm,2014,vol.5,p.1879-1886

[4]Patent:WO2017/134684,2017,A2.Locationinpatent:Page/Pagecolumn12

[5]Patent:CN103864673,2016,B.Locationinpatent:Paragraph0084;0085

[6]Patent:WO2017/12576,2017,A1.Locationinpatent:Page/Pagecolumn183

[7]Patent:WO2008/109613,2008,A1.Locationinpatent:Page/Pagecolumn217-218

[8]SyntheticCommunications,2008,vol.38,p.517-524

[9]BioorganicandMedicinalChemistryLetters,2008,vol.18,p.2215-2221

[10]Patent:EP2947086,2015,A1.Locationinpatent:Paragraph0228

[11]Patent:WO2016/79693,2016,A1.Locationinpatent:Page/Pagecolumn25

[12]Patent:CN105315283,2016,A.Locationinpatent:Paragraph0105;0112;0113;0114

[13]Patent:WO2016/170545,2016,A1.Locationinpatent:Page/Pagecolumn32;33

[14]Patent:WO2016/151438,2016,A1.Locationinpatent:Page/Pagecolumn11

[15]Patent:US2017/44166,2017,A1.Locationinpatent:Paragraph0187

[16]Patent:US2017/217970,2017,A1.Locationinpatent:Paragraph0335

[17]Patent:WO2017/137446,2017,A1.Locationinpatent:Page/Pagecolumn17;18;20;21

[18]Patent:US9782412,2017,B2.Locationinpatent:Page/Pagecolumn40

(3S)-piperidin-3-ol(R)camphorsulphonicacidsalt 
  24424-99-5    143900-44-1 

[1]CurrentPatentAssignee:PFIZERINC-WO2004/72086,2004,A2Locationinpatent:Page178

[1]Patent:CN106995446,2017,A.Locationinpatent:Paragraph0044-0046

[2]Patent:CN109232581,2019,A.Locationinpatent:Paragraph0016-0020

[3]Patent:CN106967071,2017,A.Locationinpatent:Paragraph0019

[4]Patent:US2008/214501,2008,A1.Locationinpatent:Page/Pagecolumn12

[5]OrganicandBiomolecularChemistry,2015,vol.13,p.5147-5157

[6]Patent:WO2014/22390,2014,A1.Locationinpatent:Paragraph95;98

[7]JournalofMedicinalChemistry,2015,vol.58,p.9625-9638

[8]Patent:CN105481862,2016,A.Locationinpatent:Paragraph0166;0167;0170

[9]Patent:WO2017/163257,2017,A1.Locationinpatent:Page/Pagecolumn19

[10]Patent:CN106008526,2016,A.Locationinpatent:Paragraph0016;0063;0064;0065

[11]Patent:CN107759602,2018,A.Locationinpatent:Paragraph0231;0236-0237

[1]Molecules,2018,vol.23

[2]ACSCatalysis,2017,vol.7,p.7174-7181

[3]ProcessBiochemistry,2017,vol.56,p.90-97

[4]ProcessBiochemistry,2016,vol.51,p.881-885

[5]OrganicProcessResearchandDevelopment,2014,vol.18,p.827-830

[6]RSCAdvances,2019,vol.9,p.2325-2331

[7]TetrahedronLetters,2017,vol.58,p.1644-1650

[8]OrganicLetters,2009,vol.11,p.1245-1248

[9]Patent:CN111393356,2020,A.Locationinpatent:Paragraph0063;0073-0078

[10]ProcessBiochemistry,2017,vol.58,p.137-144

Literature
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SDS
Tags:143900-44-1 Molecular Formula|143900-44-1 MDL|143900-44-1 SMILES|143900-44-1 (S)-1-Boc-3-hydroxypiperidine |Organic_Building_Blocks