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Home Amines 88950-64-5
88950-64-5,MFCD00083257
Catalog No.:AA0032KV

88950-64-5 | 1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
97%
in stock  
$8.00   $6.00
- +
5g
97%
in stock  
$11.00   $8.00
- +
10g
97%
in stock  
$18.00   $13.00
- +
25g
97%
in stock  
$43.00   $30.00
- +
100g
97%
in stock  
$169.00   $118.00
- +
  • 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:
AA0032KV
Chemical Name:
1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic acid
CAS Number:
88950-64-5
Molecular Formula:
C9H15NO4
Molecular Weight:
201.2197
MDL Number:
MFCD00083257
SMILES:
O=C(NC1(CC1)C(=O)O)OC(C)(C)C
Properties
Properties
 
BP:
347.6 °C at 760 mmHg  
Form:
Solid  
MP:
178 °C  
Storage:
2-8℃;  

Computed Properties
 
Complexity:
263  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
4  
XLogP3:
0.9  

Upstream Synthesis Route

[1]Patent:EP2865664,2015,A1,.Locationinpatent:Paragraph0088;0089

[2]Tetrahedron,2013,vol.69,#16,p.3495-3505

[1]TetrahedronLetters,1996,vol.37,#20,p.3441-3444

[2]Patent:WO2017/21922,2017,A1,.Locationinpatent:Page/Pagecolumn30;31

[3]Patent:US7202279,2007,B1,.Locationinpatent:Page/Pagecolumn50

[4]JournalofOrganicChemistry,1995,vol.60,#18,p.5790-5794

[5]Patent:US7202279,2007,B1,.Locationinpatent:Page/Pagecolumn42

[6]Patent:CN108341752,2018,A,.Locationinpatent:Paragraph0373;0374;0375;0376

[7]Patent:WO2016/178092,2016,A2,.Locationinpatent:Page/Pagecolumn46;47

[8]Synlett,2004,#14,p.2489-2492

[9]Patent:US5977075,1999,A,

[10]Patent:US4766246,1988,A,

[11]Patent:US2015/210635,2015,A1,.Locationinpatent:Paragraph0458-0460

[12]Patent:WO2006/102423,2006,A1,.Locationinpatent:Page/Pagecolumn70

[1]JournalofOrganicChemistry,2002,vol.67,#11,p.3965-3968

[2]EuropeanJournalofOrganicChemistry,2000,#18,p.3235-3245

[3]TetrahedronLetters,1993,vol.34,#26,p.4193-4196

[4]Patent:WO2006/102243,2006,A2,.Locationinpatent:Page/Pagecolumn59

[1]HelveticaChimicaActa,1992,vol.75,#4,p.1078-1084

[1]EuropeanJournalofOrganicChemistry,2000,#18,p.3235-3245

[2]Synthesis,2010,#20,p.3410-3414

[3]JournalofOrganicChemistry,2002,vol.67,#11,p.3965-3968

Downstream Synthesis Route

[1]JournalofOrganicChemistry,1989,vol.54,p.1815-1820

[1]JournaloftheAmericanChemicalSociety,2019,vol.141,p.3507-3514

[2]OrganicLetters,2015,vol.17,p.1545-1548

[3]Patent:WO2009/70485,2009,A1.Locationinpatent:Page/Pagecolumn120

[4]Patent:WO2018/227067,2018,A1.Locationinpatent:Page/Pagecolumn36

[5]Tetrahedron,1994,vol.50,p.9729-9742

[6]BioorganicandMedicinalChemistry,2003,vol.11,p.2551-2568

[7]Patent:WO2006/102243,2006,A2.Locationinpatent:Page/Pagecolumn60

[8]Patent:WO2010/31750,2010,A1.Locationinpatent:Page/Pagecolumn40

[9]Patent:WO2006/102423,2006,A1.Locationinpatent:Page/Pagecolumn70

[10]Patent:WO2019/112426,2019,A1.Locationinpatent:Paragraph00136

[1]Husbands;Suckling;Suckling[Tetrahedron,1994,vol.50,#32,p.9729-9742]

[1]SyntheticCommunications,1988,vol.18,p.141-150

[2]TetrahedronLetters,1993,vol.34,p.4193-4196

[1]SyntheticCommunications,1988,vol.18,p.141-150

[2]Patent:CN105111155,2018,B.Locationinpatent:Paragraph0033;0041;0042;0060

Literature
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SDS
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