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Home Other Building Blocks 114214-69-6
114214-69-6,MFCD02179040
Catalog No.:AA000AQ7

114214-69-6 | 1-Boc-3-hydroxymethylpyrrolidine

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$16.00   $11.00
- +
5g
97%
in stock  
$26.00   $18.00
- +
10g
97%
in stock  
$32.00   $22.00
- +
25g
97%
in stock  
$66.00   $47.00
- +
100g
97%
in stock  
$250.00   $175.00
- +
  • 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:
AA000AQ7
Chemical Name:
1-Boc-3-hydroxymethylpyrrolidine
CAS Number:
114214-69-6
Molecular Formula:
C10H19NO3
Molecular Weight:
201.2628
MDL Number:
MFCD02179040
SMILES:
OCC1CCN(C1)C(=O)OC(C)(C)C
Properties
Properties
 
BP:
285-291℃  
Form:
Solid  
Refractive Index:
1.4680 to 1.4720  
Storage:
Light sensitive;Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
210  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
3  
Undefined Atom Stereocenter Count:
1  
XLogP3:
0.8  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2013,vol.135,#38,p.14306-14312

[1]Patent:WO2004/108677,2004,A1,.Locationinpatent:Page138

[1]Patent:WO2004/108677,2004,A1,.Locationinpatent:Page138

[1]Patent:CN106588738,2017,A,.Locationinpatent:Paragraph0035;0037;0040;0045

[2]Synlett,2017,vol.28,#4,p.425-428

[3]Bioorganicandmedicinalchemistryletters,2002,vol.12,#13,p.1785-1789

[4]BioorganicandMedicinalChemistryLetters,2002,vol.12,#21,p.3235-3238

[5]BioorganicandMedicinalChemistry,2004,vol.12,#5,p.1151-1175

[6]Patent:EP500835,1996,B1,

[7]Patent:US6562811,2003,B1,

[8]Patent:US4997943,1991,A,

[9]Patent:US2004/147502,2004,A1,.Locationinpatent:Page/Pagecolumn36-37

[1]EuropeanJournalofMedicinalChemistry,2017,vol.126,p.1107-1117

[2]Patent:WO2012/76063,2012,A1,.Locationinpatent:Page/Pagecolumn54

[3]Patent:US2013/261100,2013,A1,.Locationinpatent:Paragraph0387-0388

[4]Patent:US2016/200730,2016,A1,.Locationinpatent:Paragraph0405;0406

Downstream Synthesis Route

[1]Patent:CN106588738,2017,A.Locationinpatent:Paragraph0035;0037;0040;0045

[2]Synlett,2017,vol.28,p.425-428

[3]Bioorganicandmedicinalchemistryletters,2002,vol.12,p.1785-1789

[4]BioorganicandMedicinalChemistryLetters,2002,vol.12,p.3235-3238

[5]BioorganicandMedicinalChemistry,2004,vol.12,p.1151-1175

[6]Patent:EP500835,1996,B1

[7]Patent:US6562811,2003,B1

[8]Patent:US4997943,1991,A

[9]Patent:US2004/147502,2004,A1.Locationinpatent:Page/Pagecolumn36-37

[1]BioorganicandMedicinalChemistry,2004,vol.12,p.1151-1175

957621-43-1    114214-69-6   
3-5-(4-isopropyl-piperazine-1-carbonyl)-indol-1-ylmethyl-pyrrolidine-1-carboxylicacidtert-butylester 

[1]Patent:US2007/270423,2007,A1.Locationinpatent:Page/Pagecolumn17

[1]BioorganicandMedicinalChemistry,2004,vol.12,p.1151-1175

[2]BioorganicandMedicinalChemistryLetters,2002,vol.12,p.3235-3238

[1]BioorganicandMedicinalChemistry,2004,vol.12,p.1151-1175

Literature
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Additional Info:
SDS
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