206989-61-9,MFCD08437655
Catalog No.:AA002IPI

206989-61-9 | 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$10.00   $7.00
- +
5g
98%
in stock  
$19.00   $13.00
- +
10g
98%
in stock  
$23.00   $16.00
- +
25g
98%
in stock  
$55.00   $38.00
- +
100g
≥98%
in stock  
$214.00   $150.00
- +
250g
95%
in stock  
$439.00   $308.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA002IPI
Chemical Name:
4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester
CAS Number:
206989-61-9
Molecular Formula:
C12H21NO3
Molecular Weight:
227.3000
MDL Number:
MFCD08437655
SMILES:
CC(=O)C1CCN(CC1)C(=O)OC(C)(C)C
Properties
Properties
 
BP:
312.4°C at 760 mmHg  
Form:
Liquid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
273  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.3  

Upstream Synthesis Route

[1]Patent:WO2013/96744,2013,A1,.Locationinpatent:Page/Pagecolumn192

[2]Patent:EP3255042,2017,A2,.Locationinpatent:Paragraph0209;0213

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,#4,p.935-939

[2]BioorganicandMedicinalChemistryLetters,2011,vol.21,#5,p.1299-1305

[3]Patent:EP3255042,2017,A2,.Locationinpatent:Paragraph0209;0212

[4]Patent:WO2008/17461,2008,A1,.Locationinpatent:Page/Pagecolumn62

[5]Patent:WO2008/42925,2008,A1,.Locationinpatent:Page/Pagecolumn96

[6]Patent:WO2008/42925,2008,A1,.Locationinpatent:Page/Pagecolumn96

[7]Patent:WO2009/150144,2009,A1,.Locationinpatent:Page/Pagecolumn139

[8]Patent:WO2013/96744,2013,A1,.Locationinpatent:Page/Pagecolumn191

[9]Patent:WO2016/40498,2016,A1,.Locationinpatent:Paragraph0269

[10]Patent:US2004/2504,2004,A1,.Locationinpatent:Page/Pagecolumn23;38

[11]AngewandteChemie-InternationalEdition,2017,vol.56,#23,p.6646-6650

[12]Angew.Chem.,2017,vol.56,#23,p.6646-6650,5

[13]Patent:WO2018/33135,2018,A1,.Locationinpatent:Paragraph0102-0103

[14]Patent:TW2018/11794,2018,A,.Locationinpatent:Paragraph0055;0091;0095

[15]Patent:WO2018/137681,2018,A1,.Locationinpatent:Paragraph00137;00138

[1]Patent:KR2017/45749,2017,A,.Locationinpatent:Paragraph0614;0620-0622

[2]Patent:WO2004/41777,2004,A2,.Locationinpatent:Page54-55

[3]Patent:US6140333,2000,A,

[1]Tetrahedron,2015,vol.71,#42,p.8208-8212

[1]Patent:WO2004/99178,2004,A1,.Locationinpatent:Page39

Downstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.935-939

[2]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.1299-1305

[3]Patent:EP3255042,2017,A2.Locationinpatent:Paragraph0209;0212

[4]Patent:WO2008/17461,2008,A1.Locationinpatent:Page/Pagecolumn62

[5]Patent:WO2008/42925,2008,A1.Locationinpatent:Page/Pagecolumn96

[6]Patent:WO2009/150144,2009,A1.Locationinpatent:Page/Pagecolumn139

[7]Patent:WO2013/96744,2013,A1.Locationinpatent:Page/Pagecolumn191

[8]Patent:WO2016/40498,2016,A1.Locationinpatent:Paragraph0269

[9]Patent:US2004/2504,2004,A1.Locationinpatent:Page/Pagecolumn23;38

[10]AngewandteChemie-InternationalEdition,2017,vol.56,p.6646-6650    Angew.Chem.,2017,vol.56,p.6646-6650,5

[11]Patent:WO2018/33135,2018,A1.Locationinpatent:Paragraph0102-0103

[12]Patent:TW2018/11794,2018,A.Locationinpatent:Paragraph0055;0091;0095

[13]Patent:WO2018/137681,2018,A1.Locationinpatent:Paragraph00137;00138

[14]Patent:WO2019/108795,2019,A1.Locationinpatent:Paragraph0109

[1]JournalofMedicinalChemistry,2004,vol.47,p.3111-3130

[1]Patent:WO2009/150144,2009,A1.Locationinpatent:Page/Pagecolumn139

[2]TetrahedronLetters,2012,vol.53,p.852-853

[3]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.3419-3424

[4]Patent:WO2004/41279,2004,A1.Locationinpatent:Page/Pagecolumn70

[5]Patent:WO2015/88565,2015,A1.Locationinpatent:Paragraph00214

[6]Patent:WO2008/42925,2008,A1

[1]ChemicalandPharmaceuticalBulletin,2001,vol.49,p.822-829

2524-52-9    206989-61-9   
tert-butyl4-(3-oxo-3-pyridin-2-ylpropanoyl)piperidine-1-carboxylate 

[1]CurrentPatentAssignee:MERCK&COINC-WO2005/100344,2005,A1Locationinpatent:Page/Pagecolumn40-41

Literature
Quotation Request
Company Name:
*
Contact Person:
*
Email:
*
Quantity Required:
*
Country:
Additional Info:
SDS
Historical Records
Tags:206989-61-9 Molecular Formula|206989-61-9 MDL|206989-61-9 SMILES|206989-61-9 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester
Catalog No.: AA002IPI
206989-61-9,MFCD08437655
206989-61-9 | 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester
Pack Size: 1g
Purity: 98%
in stock
$10.00 $7.00
Pack Size: 5g
Purity: 98%
in stock
$19.00 $13.00
Pack Size: 10g
Purity: 98%
in stock
$23.00 $16.00
Pack Size: 25g
Purity: 98%
in stock
$55.00 $38.00
Pack Size: 100g
Purity: ≥98%
in stock
$214.00 $150.00
Pack Size: 250g
Purity: 95%
in stock
$439.00 $308.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA002IPI
Chemical Name: 4-Acetyl-piperidine-1-carboxylic acid tert-butyl ester
CAS Number: 206989-61-9
Molecular Formula: C12H21NO3
Molecular Weight: 227.3000
MDL Number: MFCD08437655
SMILES: CC(=O)C1CCN(CC1)C(=O)OC(C)(C)C
Properties
BP: 312.4°C at 760 mmHg  
Form: Liquid  
Storage: Keep in dry area;Room Temperature;  
Complexity: 273  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 16  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.3  
Upstream Synthesis Route
206989-61-9    89895-06-7 

[1]Patent:WO2013/96744,2013,A1,.Locationinpatent:Page/Pagecolumn192

[2]Patent:EP3255042,2017,A2,.Locationinpatent:Paragraph0209;0213

75-16-1    139290-70-3    206989-61-9 

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,#4,p.935-939

[2]BioorganicandMedicinalChemistryLetters,2011,vol.21,#5,p.1299-1305

[3]Patent:EP3255042,2017,A2,.Locationinpatent:Paragraph0209;0212

[4]Patent:WO2008/17461,2008,A1,.Locationinpatent:Page/Pagecolumn62

[5]Patent:WO2008/42925,2008,A1,.Locationinpatent:Page/Pagecolumn96

[6]Patent:WO2008/42925,2008,A1,.Locationinpatent:Page/Pagecolumn96

[7]Patent:WO2009/150144,2009,A1,.Locationinpatent:Page/Pagecolumn139

[8]Patent:WO2013/96744,2013,A1,.Locationinpatent:Page/Pagecolumn191

[9]Patent:WO2016/40498,2016,A1,.Locationinpatent:Paragraph0269

[10]Patent:US2004/2504,2004,A1,.Locationinpatent:Page/Pagecolumn23;38

[11]AngewandteChemie-InternationalEdition,2017,vol.56,#23,p.6646-6650

[12]Angew.Chem.,2017,vol.56,#23,p.6646-6650,5

[13]Patent:WO2018/33135,2018,A1,.Locationinpatent:Paragraph0102-0103

[14]Patent:TW2018/11794,2018,A,.Locationinpatent:Paragraph0055;0091;0095

[15]Patent:WO2018/137681,2018,A1,.Locationinpatent:Paragraph00137;00138

139290-70-3    206989-61-9 

[1]Patent:KR2017/45749,2017,A,.Locationinpatent:Paragraph0614;0620-0622

[2]Patent:WO2004/41777,2004,A2,.Locationinpatent:Page54-55

[3]Patent:US6140333,2000,A,

479630-08-5    206989-61-9 

[1]Tetrahedron,2015,vol.71,#42,p.8208-8212

75-16-1    91419-52-2    206989-61-9 

[1]Patent:WO2004/99178,2004,A1,.Locationinpatent:Page39

Downstream Synthesis Route
75-16-1    139290-70-3    206989-61-9 

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.935-939

[2]BioorganicandMedicinalChemistryLetters,2011,vol.21,p.1299-1305

[3]Patent:EP3255042,2017,A2.Locationinpatent:Paragraph0209;0212

[4]Patent:WO2008/17461,2008,A1.Locationinpatent:Page/Pagecolumn62

[5]Patent:WO2008/42925,2008,A1.Locationinpatent:Page/Pagecolumn96

[6]Patent:WO2009/150144,2009,A1.Locationinpatent:Page/Pagecolumn139

[7]Patent:WO2013/96744,2013,A1.Locationinpatent:Page/Pagecolumn191

[8]Patent:WO2016/40498,2016,A1.Locationinpatent:Paragraph0269

[9]Patent:US2004/2504,2004,A1.Locationinpatent:Page/Pagecolumn23;38

[10]AngewandteChemie-InternationalEdition,2017,vol.56,p.6646-6650    Angew.Chem.,2017,vol.56,p.6646-6650,5

[11]Patent:WO2018/33135,2018,A1.Locationinpatent:Paragraph0102-0103

[12]Patent:TW2018/11794,2018,A.Locationinpatent:Paragraph0055;0091;0095

[13]Patent:WO2018/137681,2018,A1.Locationinpatent:Paragraph00137;00138

[14]Patent:WO2019/108795,2019,A1.Locationinpatent:Paragraph0109

2905-54-6    206989-61-9    767321-32-4 

[1]JournalofMedicinalChemistry,2004,vol.47,p.3111-3130

206989-61-9    301221-79-4 

[1]Patent:WO2009/150144,2009,A1.Locationinpatent:Page/Pagecolumn139

[2]TetrahedronLetters,2012,vol.53,p.852-853

[3]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.3419-3424

[4]Patent:WO2004/41279,2004,A1.Locationinpatent:Page/Pagecolumn70

[5]Patent:WO2015/88565,2015,A1.Locationinpatent:Paragraph00214

[6]Patent:WO2008/42925,2008,A1

91419-48-6    206989-61-9 

[1]ChemicalandPharmaceuticalBulletin,2001,vol.49,p.822-829

2524-52-9    206989-61-9   
tert-butyl4-(3-oxo-3-pyridin-2-ylpropanoyl)piperidine-1-carboxylate 

[1]CurrentPatentAssignee:MERCK&COINC-WO2005/100344,2005,A1Locationinpatent:Page/Pagecolumn40-41

Building Blocks More >
207511-08-8
207511-08-8
Maltotriose hydrate
AA002J0B | MFCD00006629
207853-61-0
207853-61-0
2,5-Difluoromandelic acid
AA002J99 | MFCD00061297
208264-60-2
208264-60-2
ethyl 2,5-dibromo-1,3-thiazole-4-carboxylate
AA002JJF | MFCD09265487
208772-41-2
208772-41-2
1-(tert-Butoxycarbonyl)indoline-6-carboxylic acid
AA002JT2 | MFCD09878909
20937-44-4
20937-44-4
Cyclopentanamine, 1-(phenylmethyl)-, hydrochloride (1:1)
AA002K4V | MFCD01735698
209984-57-6
209984-57-6
Ly411575
AA002KFF | MFCD09832551
2104-04-3
2104-04-3
4-(4-Methoxyphenyl)-1,3-thiazol-2-amine
AA002KOU | MFCD00170663
21088-15-3
21088-15-3
1-(3,4-Diethoxybenzyl)-6,7-diethoxy-1,2,3,4-tetrahydroisoquinoline hydrochloride
AA002KXV | MFCD04610442
2114-18-3
2114-18-3
Ethanol, 2-chloro-, 1-carbamate
AA002L9A | MFCD00025467
22940-86-9
22940-86-9
1-(3,5-Dimethylfuran-2-yl)ethanone
AA002LJH | MFCD00052576
Submit
© 2017 AA BLOCKS, INC. All rights reserved.