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106391-86-0,MFCD00235912
Catalog No.:AA0035A3

106391-86-0 | Boc-D-Alaninol

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1g
97%
in stock  
$6.00   $4.00
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5g
97%
in stock  
$7.00   $5.00
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10g
97%
in stock  
$13.00   $9.00
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25g
97%
in stock  
$27.00   $19.00
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50g
95%
in stock  
$38.00   $27.00
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100g
95%
in stock  
$65.00   $46.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA0035A3
Chemical Name:
Boc-D-Alaninol
CAS Number:
106391-86-0
Molecular Formula:
C8H17NO3
Molecular Weight:
175.2255
MDL Number:
MFCD00235912
SMILES:
OC[C@H](NC(=O)OC(C)(C)C)C
Properties
Properties
 
BP:
276.4°C at 760 mmHg  
Form:
Solid  
MP:
58-61 °C  
Storage:
Room Temperature;Light sensitive;Inert atmosphere;  

Computed Properties
 
Complexity:
151  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
12  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
4  
XLogP3:
0.7  

Downstream Synthesis Route
338-69-2    24424-99-5   
(R)-2-tertbutoxycarbonylamino-1-propanol 

[1]CurrentPatentAssignee:ROCHEHOLDINGAG-WO2008/55840,2008,A1Locationinpatent:Page/Pagecolumn58

[2]CurrentPatentAssignee:ROCHEHOLDINGAG-US2009/163502,2009,A1Locationinpatent:Page/Pagecolumn40

[3]CurrentPatentAssignee:ROCHEHOLDINGAG-US2009/163499,2009,A1Locationinpatent:Page/Pagecolumn28

[4]CurrentPatentAssignee:ROCHEHOLDINGAG-US2009/170873,2009,A1Locationinpatent:Page/Pagecolumn42

[5]CurrentPatentAssignee:ROCHEHOLDINGAG-US2010/324069,2010,A1Locationinpatent:Page/Pagecolumn24

[6]CurrentPatentAssignee:ROCHEHOLDINGAG-US2010/324070,2010,A1Locationinpatent:Page/Pagecolumn19-20

[7]CurrentPatentAssignee:ROCHEHOLDINGAG-US2010/324056,2010,A1Locationinpatent:Page/Pagecolumn30

[8]CurrentPatentAssignee:ROCHEHOLDINGAG-US2012/22067,2012,A1Locationinpatent:Page/Pagecolumn36

Literature

Title: Chiral oxime ethers in asymmetric synthesis. O-(1-Phenylbutyl)benzyloxyacetaldoxime, a versatile reagent for the asymmetric synthesis of protected 1,2-aminoalcohols, alpha-amino acid derivatives, and 2-hydroxymethyl nitrogen heterocycles including iminosugars.

Journal: Organic & biomolecular chemistry 20050407

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SDS
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