140695-84-7,MFCD02683203
Catalog No.:AA007ZOR

140695-84-7 | tert-Butyl (3S)-3-(hydroxymethyl)piperidine-1-carboxylate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
98%
in stock  
$6.00   $4.00
- +
1g
98%
in stock  
$15.00   $11.00
- +
5g
98%
in stock  
$19.00   $13.00
- +
10g
98%
in stock  
$35.00   $25.00
- +
25g
98%
in stock  
$87.00   $61.00
- +
100g
98%
in stock  
$347.00   $243.00
- +
250g
95%
in stock  
$836.00   $585.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA007ZOR
Chemical Name:
tert-Butyl (3S)-3-(hydroxymethyl)piperidine-1-carboxylate
CAS Number:
140695-84-7
Molecular Formula:
C11H21NO3
Molecular Weight:
215.2893
MDL Number:
MFCD02683203
SMILES:
OC[C@H]1CCCN(C1)C(=O)OC(C)(C)C
Properties
Computed Properties
 
Complexity:
222  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
15  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Isotope Atom Count:
0  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
1.2  

Upstream Synthesis Route

[1]Tetrahedron:Asymmetry,1992,vol.3,#8,p.1049-1054

[2]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

[1]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

[2]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

[1]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,#8,p.1927-1930

[1]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

[2]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

Downstream Synthesis Route

[1]TetrahedronAsymmetry,1992,vol.3,p.1049-1054

[2]OrganicProcessResearchandDevelopment,2001,vol.5,p.415-420

[1]Park,Jin-Seong;Yeom,Chang-Eun;Choi,SooHyuk;Ahn,YongShik;Ro,Sunggu;Jeon,YoungHo;Shin,Dong-Kyu;Kim,B.Moon[TetrahedronLetters,2003,vol.44,#8,p.1611-1614]

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.1927-1930

[1]Patent:WO2008/23258,2008,A1.Locationinpatent:Page/Pagecolumn43-44

[2]Patent:WO2008/23258,2008,A1.Locationinpatent:Page/Pagecolumn40

[1]CurrentPatentAssignee:PFIZERINC-WO2008/23258,2008,A1Locationinpatent:Page/Pagecolumn50

Literature
Quotation Request
Company Name:
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Contact Person:
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Email:
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Quantity Required:
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Additional Info:
SDS
Tags:140695-84-7 Molecular Formula|140695-84-7 MDL|140695-84-7 SMILES|140695-84-7 tert-Butyl (3S)-3-(hydroxymethyl)piperidine-1-carboxylate
Catalog No.: AA007ZOR
140695-84-7,MFCD02683203
140695-84-7 | tert-Butyl (3S)-3-(hydroxymethyl)piperidine-1-carboxylate
Pack Size: 250mg
Purity: 98%
in stock
$6.00 $4.00
Pack Size: 1g
Purity: 98%
in stock
$15.00 $11.00
Pack Size: 5g
Purity: 98%
in stock
$19.00 $13.00
Pack Size: 10g
Purity: 98%
in stock
$35.00 $25.00
Pack Size: 25g
Purity: 98%
in stock
$87.00 $61.00
Pack Size: 100g
Purity: 98%
in stock
$347.00 $243.00
Pack Size: 250g
Purity: 95%
in stock
$836.00 $585.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA007ZOR
Chemical Name: tert-Butyl (3S)-3-(hydroxymethyl)piperidine-1-carboxylate
CAS Number: 140695-84-7
Molecular Formula: C11H21NO3
Molecular Weight: 215.2893
MDL Number: MFCD02683203
SMILES: OC[C@H]1CCCN(C1)C(=O)OC(C)(C)C
Properties
Complexity: 222  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 1  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 15  
Hydrogen Bond Acceptor Count: 3  
Hydrogen Bond Donor Count: 1  
Isotope Atom Count: 0  
Rotatable Bond Count: 3  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 1.2  
Upstream Synthesis Route
140645-20-1    116574-71-1    140695-84-7 

[1]Tetrahedron:Asymmetry,1992,vol.3,#8,p.1049-1054

[2]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

140645-20-1    116574-71-1    140695-84-7    140695-98-3 

[1]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

[2]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

4606-65-9    24424-99-5    116574-71-1    140695-84-7 

[1]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

108-05-4    116574-71-1    116574-71-1    140695-84-7    144448-01-1 

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,#8,p.1927-1930

108-30-5    116574-71-1    116574-71-1    140695-84-7 

[1]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

[2]OrganicProcessResearchandDevelopment,2001,vol.5,#4,p.415-420

Downstream Synthesis Route
140645-20-1    116574-71-1    140695-84-7 

[1]TetrahedronAsymmetry,1992,vol.3,p.1049-1054

[2]OrganicProcessResearchandDevelopment,2001,vol.5,p.415-420

88466-76-6    140695-84-7 

[1]Park,Jin-Seong;Yeom,Chang-Eun;Choi,SooHyuk;Ahn,YongShik;Ro,Sunggu;Jeon,YoungHo;Shin,Dong-Kyu;Kim,B.Moon[TetrahedronLetters,2003,vol.44,#8,p.1611-1614]

108-05-4    116574-71-1    116574-71-1    140695-84-7    144448-01-1 

[1]BioorganicandMedicinalChemistryLetters,2004,vol.14,p.1927-1930

23003-30-7    140695-84-7    1008562-77-3 

[1]Patent:WO2008/23258,2008,A1.Locationinpatent:Page/Pagecolumn43-44

[2]Patent:WO2008/23258,2008,A1.Locationinpatent:Page/Pagecolumn40

6272-38-4    140695-84-7    1008563-00-5 

[1]CurrentPatentAssignee:PFIZERINC-WO2008/23258,2008,A1Locationinpatent:Page/Pagecolumn50

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