Name: Name:1-[(tert-Butoxycarbonyl)amino]cyclopropanecarboxylic acid
Brand: AABLOCKS
SKU: AA0032KV
Rating: 90 (10 reviews)

Catalog No.: AA0032KV

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

Pack Size： 1g

Purity： 97%

in stock

$8.00 $6.00

Pack Size： 5g

Purity： 97%

in stock

$11.00 $8.00

Pack Size： 10g

Purity： 97%

in stock

$19.00 $13.00

Pack Size： 25g

Purity： 97%

in stock

$43.00 $31.00

Pack Size： 100g

Purity： 97%

in stock

$171.00 $120.00

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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

BP: 347.6 °C at 760 mmHg

Form: Solid

MP: 178 °C

Storage: 2-8℃;

Complexity: 263

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 14

Hydrogen Bond Acceptor Count: 4

Hydrogen Bond Donor Count: 2

Isotope Atom Count: 0

Rotatable Bond Count: 4

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 0.9

109:

Upstream Synthesis Route

24424-99-5

68781-13-5

88950-64-5

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

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

24424-99-5

22059-21-8

88950-64-5

[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

24424-99-5

88950-64-5

[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

143521-34-0

88950-64-5

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

107017-73-2

88950-64-5

[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

22059-21-8

58632-95-4

88950-64-5

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

6638-79-5

88950-64-5

161521-10-4

[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

68781-13-5

58632-95-4

88950-64-5

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

88950-64-5

22059-21-8

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

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

107259-05-2

88950-64-5

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

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

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