75844-69-8,MFCD02093935
Catalog No.:AA0038DB

75844-69-8 | tert-butyl piperidine-1-carboxylate

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Purity
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Price(USD)
Quantity
  
1g
98%
in stock  
$11.00   $8.00
- +
5g
98%
in stock  
$15.00   $11.00
- +
10g
98%
in stock  
$21.00   $15.00
- +
100g
95%
in stock  
$202.00   $142.00
- +
500g
95%
in stock  
$774.00 $542.00
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0038DB
Chemical Name:
tert-butyl piperidine-1-carboxylate
CAS Number:
75844-69-8
Molecular Formula:
C10H19NO2
Molecular Weight:
185.2634
MDL Number:
MFCD02093935
SMILES:
O=C(N1CCCCC1)OC(C)(C)C
Properties
Computed Properties
 
Complexity:
178  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
2  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
2  

Downstream Synthesis Route

[1]Synthesis,2006,p.2784-2788

[2]TetrahedronLetters,2007,vol.48,p.8318-8322

[3]TetrahedronLetters,2008,vol.49,p.2527-2532

[4]TetrahedronLetters,2011,vol.52,p.1260-1264

[5]MonatsheftefurChemie,2011,vol.142,p.1035-1043

[6]AsianJournalofChemistry,2017,vol.29,p.1313-1316

[7]Chemistry-AEuropeanJournal,2019,vol.25,p.16120-16127

[8]TetrahedronLetters,2006,vol.47,p.455-458

[9]TetrahedronLetters,2010,vol.51,p.3855-3858

[10]RSCAdvances,2016,vol.6,p.78576-78584

[11]JournaloftheAmericanChemicalSociety,2010,vol.132,p.7260-7261

[12]JournalofOrganicChemistry,1997,vol.62,p.7726-7735

[13]OrganicLetters,2013,vol.15,p.1918-1921

[14]JournalofChemicalResearch,2013,vol.37,p.757-760

[15]OrganicandBiomolecularChemistry,2018,vol.16,p.1971-1975

[16]OrganicLetters,2006,vol.8,p.3259-3262

[17]TetrahedronLetters,2008,vol.49,p.3527-3529

[18]Synthesis,2008,p.3126-3130

[19]OrganicandBiomolecularChemistry,2017,vol.15,p.5364-5372

[20]Tetrahedron,2001,vol.57,p.9033-9043

[21]Synlett,2007,p.806-808

[22]LettersinOrganicChemistry,2011,vol.8,p.38-42

[23]OrganicandBiomolecularChemistry,2016,vol.14,p.7084-7091

[24]NewJournalofChemistry,2018,vol.42,p.10142-10147

[25]JournalofOrganicChemistry,1993,vol.58,p.1109-1117

[26]Synlett,2006,p.1110-1112

[27]TetrahedronLetters,2004,vol.45,p.6963-6965

[28]MonatsheftefurChemie,2012,vol.143,p.631-635

[29]RSCAdvances,2015,vol.5,p.19790-19798

[30]JournalofOrganicChemistry,2006,vol.71,p.8283-8286

[31]JournaloftheIranianChemicalSociety,2012,vol.9,p.495-502

[32]OrganicLetters,2010,vol.12,p.4176-4179

[33]JournaloftheAmericanChemicalSociety,2017,vol.139,p.8267-8276

[34]SyntheticCommunications,2015,vol.45,p.653-660

[35]SyntheticCommunications,1989,vol.19,p.3139-3142

[36]JournaloftheChemicalSociety.PerkintransactionsI,1998,p.1463-1464

[37]Patent:US6369078,2002,B1

[38]BulletinoftheKoreanChemicalSociety,2010,vol.31,p.735-738

[39]OrganicLetters,2018,vol.20,p.5661-5665

[40]JournalofOrganicChemistry,2020,vol.85,p.4740-4752

[1]JournalofOrganicChemistry,2010,vol.75,p.4069-4077

[2]ACSCatalysis,2019,vol.9,p.9513-9517

[3]TetrahedronLetters,1990,vol.31,p.6385-6386

[4]OrganicLetters,2013,vol.15,p.1918-1921

75844-69-8    131667-57-7   
tert-butyl2-azidopiperidine-1-carboxylate 

[1]Magnus,Philip;Hulme,Christopher;Weber,Wolfgang[JournaloftheAmericanChemicalSociety,1994,vol.116,#10,p.4501-4502]

[1]OrganicLetters,2014,vol.16,p.4618-4621

[2]ChemistryLetters,2009,vol.38,p.160-161

[3]TetrahedronLetters,2006,vol.47,p.455-458

[4]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.2163-2165

[5]JournalofAgriculturalandFoodChemistry,2014,vol.62,p.1233-1239

[1]BertiniGross;Beak[JournaloftheAmericanChemicalSociety,2001,vol.123,#2,p.315-321]

Literature

Title: Dynamics of catalytic resolution of 2-lithio-N-Boc-piperidine by ligand exchange.

Journal: Journal of the American Chemical Society 20121010

Title: Regioselective and stereoselective copper(I)-promoted allylation and conjugate addition of N-Boc-2-lithiopyrrolidine and N-Boc-2-lithiopiperidine.

Journal: The Journal of organic chemistry 20100618

Title: Asymmetric deprotonation of N-boc piperidine: react IR monitoring and mechanistic aspects.

Journal: Journal of the American Chemical Society 20100602

Title: Asymmetric substitutions of 2-lithiated N-boc-piperidine and N-Boc-azepine by dynamic resolution.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany) 20100406

Title: Synthesis of 2-arylpiperidines by palladium couplings of aryl bromides with organozinc species derived from deprotonation of N-boc-piperidine.

Journal: Organic letters 20080904

Title: Dynamic kinetic and kinetic resolution of N-Boc-2-lithiopiperidine.

Journal: Chemical communications (Cambridge, England) 20071121

Title: An experimental and theoretical study of the asymmetric lithiation of 1,2,3,5,6,7-hexahydro-3a,4a-diazacyclopenta[def]phenanthren-4-one.

Journal: The Journal of organic chemistry 20070202

Title: Reactivity series for s-BuLi/diamine-mediated lithiation of N-Boc pyrrolidine: applications in catalysis and lithiation of N-Boc piperidine.

Journal: Chemical communications (Cambridge, England) 20060628

Title: Synthesis of methylphenidate analogues and their binding affinities at dopamine and serotonin transport sites.

Journal: Bioorganic & medicinal chemistry letters 20040405

Title: An experimental and computational investigation of the enantioselective deprotonation of Boc-piperidine.

Journal: Journal of the American Chemical Society 20020306

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Additional Info:
SDS
Historical Records
Tags:75844-69-8 Molecular Formula|75844-69-8 MDL|75844-69-8 SMILES|75844-69-8 tert-butyl piperidine-1-carboxylate
Catalog No.: AA0038DB
75844-69-8,MFCD02093935
75844-69-8 | tert-butyl piperidine-1-carboxylate
Pack Size: 1g
Purity: 98%
in stock
$11.00 $8.00
Pack Size: 5g
Purity: 98%
in stock
$15.00 $11.00
Pack Size: 10g
Purity: 98%
in stock
$21.00 $15.00
Pack Size: 100g
Purity: 95%
in stock
$202.00 $142.00
Pack Size: 500g
Purity: 95%
in stock
$774.00 $542.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0038DB
Chemical Name: tert-butyl piperidine-1-carboxylate
CAS Number: 75844-69-8
Molecular Formula: C10H19NO2
Molecular Weight: 185.2634
MDL Number: MFCD02093935
SMILES: O=C(N1CCCCC1)OC(C)(C)C
Properties
Complexity: 178  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 13  
Hydrogen Bond Acceptor Count: 2  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 2  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 2  
Downstream Synthesis Route
110-89-4    24424-99-5    75844-69-8 

[1]Synthesis,2006,p.2784-2788

[2]TetrahedronLetters,2007,vol.48,p.8318-8322

[3]TetrahedronLetters,2008,vol.49,p.2527-2532

[4]TetrahedronLetters,2011,vol.52,p.1260-1264

[5]MonatsheftefurChemie,2011,vol.142,p.1035-1043

[6]AsianJournalofChemistry,2017,vol.29,p.1313-1316

[7]Chemistry-AEuropeanJournal,2019,vol.25,p.16120-16127

[8]TetrahedronLetters,2006,vol.47,p.455-458

[9]TetrahedronLetters,2010,vol.51,p.3855-3858

[10]RSCAdvances,2016,vol.6,p.78576-78584

[11]JournaloftheAmericanChemicalSociety,2010,vol.132,p.7260-7261

[12]JournalofOrganicChemistry,1997,vol.62,p.7726-7735

[13]OrganicLetters,2013,vol.15,p.1918-1921

[14]JournalofChemicalResearch,2013,vol.37,p.757-760

[15]OrganicandBiomolecularChemistry,2018,vol.16,p.1971-1975

[16]OrganicLetters,2006,vol.8,p.3259-3262

[17]TetrahedronLetters,2008,vol.49,p.3527-3529

[18]Synthesis,2008,p.3126-3130

[19]OrganicandBiomolecularChemistry,2017,vol.15,p.5364-5372

[20]Tetrahedron,2001,vol.57,p.9033-9043

[21]Synlett,2007,p.806-808

[22]LettersinOrganicChemistry,2011,vol.8,p.38-42

[23]OrganicandBiomolecularChemistry,2016,vol.14,p.7084-7091

[24]NewJournalofChemistry,2018,vol.42,p.10142-10147

[25]JournalofOrganicChemistry,1993,vol.58,p.1109-1117

[26]Synlett,2006,p.1110-1112

[27]TetrahedronLetters,2004,vol.45,p.6963-6965

[28]MonatsheftefurChemie,2012,vol.143,p.631-635

[29]RSCAdvances,2015,vol.5,p.19790-19798

[30]JournalofOrganicChemistry,2006,vol.71,p.8283-8286

[31]JournaloftheIranianChemicalSociety,2012,vol.9,p.495-502

[32]OrganicLetters,2010,vol.12,p.4176-4179

[33]JournaloftheAmericanChemicalSociety,2017,vol.139,p.8267-8276

[34]SyntheticCommunications,2015,vol.45,p.653-660

[35]SyntheticCommunications,1989,vol.19,p.3139-3142

[36]JournaloftheChemicalSociety.PerkintransactionsI,1998,p.1463-1464

[37]Patent:US6369078,2002,B1

[38]BulletinoftheKoreanChemicalSociety,2010,vol.31,p.735-738

[39]OrganicLetters,2018,vol.20,p.5661-5665

[40]JournalofOrganicChemistry,2020,vol.85,p.4740-4752

75844-69-8    131667-57-7 

[1]JournalofOrganicChemistry,2010,vol.75,p.4069-4077

[2]ACSCatalysis,2019,vol.9,p.9513-9517

[3]TetrahedronLetters,1990,vol.31,p.6385-6386

[4]OrganicLetters,2013,vol.15,p.1918-1921

75844-69-8    131667-57-7   
tert-butyl2-azidopiperidine-1-carboxylate 

[1]Magnus,Philip;Hulme,Christopher;Weber,Wolfgang[JournaloftheAmericanChemicalSociety,1994,vol.116,#10,p.4501-4502]

67-56-1    75844-69-8    195964-51-3 

[1]OrganicLetters,2014,vol.16,p.4618-4621

[2]ChemistryLetters,2009,vol.38,p.160-161

[3]TetrahedronLetters,2006,vol.47,p.455-458

[4]JournaloftheChemicalSociety.PerkintransactionsI,1997,p.2163-2165

[5]JournalofAgriculturalandFoodChemistry,2014,vol.62,p.1233-1239

815-24-7    75844-69-8    325794-29-4 

[1]BertiniGross;Beak[JournaloftheAmericanChemicalSociety,2001,vol.123,#2,p.315-321]

Literature fold

Title: Dynamics of catalytic resolution of 2-lithio-N-Boc-piperidine by ligand exchange.

Journal: Journal of the American Chemical Society20121010

Title: Regioselective and stereoselective copper(I)-promoted allylation and conjugate addition of N-Boc-2-lithiopyrrolidine and N-Boc-2-lithiopiperidine.

Journal: The Journal of organic chemistry20100618

Title: Asymmetric deprotonation of N-boc piperidine: react IR monitoring and mechanistic aspects.

Journal: Journal of the American Chemical Society20100602

Title: Asymmetric substitutions of 2-lithiated N-boc-piperidine and N-Boc-azepine by dynamic resolution.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)20100406

Title: Synthesis of 2-arylpiperidines by palladium couplings of aryl bromides with organozinc species derived from deprotonation of N-boc-piperidine.

Journal: Organic letters20080904

Title: Dynamic kinetic and kinetic resolution of N-Boc-2-lithiopiperidine.

Journal: Chemical communications (Cambridge, England)20071121

Title: An experimental and theoretical study of the asymmetric lithiation of 1,2,3,5,6,7-hexahydro-3a,4a-diazacyclopenta[def]phenanthren-4-one.

Journal: The Journal of organic chemistry20070202

Title: Reactivity series for s-BuLi/diamine-mediated lithiation of N-Boc pyrrolidine: applications in catalysis and lithiation of N-Boc piperidine.

Journal: Chemical communications (Cambridge, England)20060628

Title: Synthesis of methylphenidate analogues and their binding affinities at dopamine and serotonin transport sites.

Journal: Bioorganic & medicinal chemistry letters20040405

Title: An experimental and computational investigation of the enantioselective deprotonation of Boc-piperidine.

Journal: Journal of the American Chemical Society20020306

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