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Home Amines 7536-55-2
7536-55-2,MFCD00038152
Catalog No.:AA00ICJR

7536-55-2 | Boc-(s)-2-aminosuccinic acid 4-amide monohydrate

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
98%
in stock  
$7.00   $5.00
- +
100g
98%
in stock  
$33.00   $23.00
- +
500g
98%
in stock  
$161.00   $113.00
- +
  • 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:
AA00ICJR
Chemical Name:
Boc-(s)-2-aminosuccinic acid 4-amide monohydrate
CAS Number:
7536-55-2
Molecular Formula:
C9H16N2O5
Molecular Weight:
232.2337
MDL Number:
MFCD00038152
SMILES:
O=C(OC(C)(C)C)N[C@H](C(=O)O)CC(=O)N
Properties
Computed Properties
 
Complexity:
295  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
6  
XLogP3:
-0.6  

Upstream Synthesis Route

[1]TetrahedronLetters,2014,vol.55,#30,p.4149-4151

[1]Patent:WO2005/21558,2005,A2,.Locationinpatent:Page/Pagecolumn214

[2]Patent:US2006/189806,2006,A1,.Locationinpatent:Page/Pagecolumn38

[3]BioorganicandMedicinalChemistry,1998,vol.6,#8,p.1185-1208

[4]AngewandteChemie-InternationalEdition,2007,vol.46,#14,p.2470-2477

[5]OrganicSyntheses,1985,vol.63,p.160-160

[6]JournalofPeptideScience,2017,vol.23,#3,p.202-214

[7]BioorganicandMedicinalChemistry,2006,vol.14,#19,p.6586-6592

[8]AsianJournalofChemistry,2014,vol.26,#19,p.6541-6548

[9]ChemistryofNaturalCompounds,1979,vol.15,p.471-476

[10]KhimiyaPrirodnykhSoedinenii,1979,vol.15,p.543-548

[11]JournalofOrganicChemistry,1985,vol.50,#8,p.1239-1246

[12]ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1986,vol.40,#4,p.242-249

[13]ChineseChemicalLetters,2012,vol.23,#3,p.297-300

[14]BulletinoftheKoreanChemicalSociety,2012,vol.33,#8,p.2777-2780

[15]JournalofMedicinalChemistry,2013,vol.56,#7,p.2936-2947

[16]JournaloftheAmericanChemicalSociety,2014,vol.136,#26,p.9244-9247

[17]Patent:CN106187819,2016,A,.Locationinpatent:Paragraph024;0025;0026;0027

[1]OrganicLetters,2005,vol.7,#9,p.1723-1724

[1]BulletinoftheChemicalSocietyofJapan,1989,vol.62,#10,p.3103-3108

[1]Synthesis,1974,p.661-662

[2]JustusLiebigsAnnalenderChemie,1964,vol.673,p.208-220

Downstream Synthesis Route

[1]Patent:WO2005/21558,2005,A2.Locationinpatent:Page/Pagecolumn214

[2]Patent:US2006/189806,2006,A1.Locationinpatent:Page/Pagecolumn38

[3]BioorganicandMedicinalChemistry,1998,vol.6,p.1185-1208

[4]AngewandteChemie-InternationalEdition,2007,vol.46,p.2470-2477

[5]OrganicSyntheses,1985,vol.63,p.160-160

[6]JournalofPeptideScience,2017,vol.23,p.202-214

[7]BioorganicandMedicinalChemistry,2006,vol.14,p.6586-6592

[8]AsianJournalofChemistry,2014,vol.26,p.6541-6548

[9]ChemistryofNaturalCompounds,1979,vol.15,p.471-476    KhimiyaPrirodnykhSoedinenii,1979,vol.15,p.543-548

[10]JournalofOrganicChemistry,1985,vol.50,p.1239-1246

[11]ActachemicaScandinavica.SeriesB:Organicchemistryandbiochemistry,1986,vol.40,p.242-249

[12]ChineseChemicalLetters,2012,vol.23,p.297-300

[13]BulletinoftheKoreanChemicalSociety,2012,vol.33,p.2777-2780

[14]JournalofMedicinalChemistry,2013,vol.56,p.2936-2947

[15]JournaloftheAmericanChemicalSociety,2014,vol.136,p.9244-9247

[16]Patent:CN106187819,2016,A.Locationinpatent:Paragraph024;0025;0026;0027

[17]BioorganicChemistry,2019,vol.87,p.209-217

[18]Patent:CN109748813,2019,A.Locationinpatent:Paragraph0010;0011;0018

[19]AminoAcids,2020,vol.52,p.55-72

[1]Chemicalandpharmaceuticalbulletin,1981,vol.29,p.2825-2831

[1]JournalofMedicinalChemistry,1990,vol.33,p.1285-1288

[1]JournalofOrganicChemistry,1997,vol.62,p.4721-4736

[2]BioorganicandMedicinalChemistry,2006,vol.14,p.304-318

[3]JournalofOrganicChemistry,1990,vol.55,p.3186-3194

[4]TetrahedronLetters,1982,vol.23,p.149-152

[5]JournalofOrganicChemistry,1980,vol.45,p.555-560

[6]JournalofMedicinalChemistry,1997,vol.40,p.2064-2084

[7]Patent:WO2012/146667,2012,A1.Locationinpatent:Page/Pagecolumn110

[1]OrganicandBiomolecularChemistry,2015,vol.13,p.1629-1633

[2]ChemicalCommunications,2011,vol.47,p.1198-1200

[3]JournalofOrganicChemistry,2012,vol.77,p.5696-5704

[4]Synlett,2008,p.513-516

[5]NewJournalofChemistry,2019,vol.43,p.18442-18444

[6]JournalofPeptideScience,2017,vol.23,p.202-214

[7]BioorganicandMedicinalChemistry,1999,vol.7,p.161-175

[8]OrganicLetters,2007,vol.9,p.25-28

[9]Patent:WO2020/10021,2020,A1.Locationinpatent:Page/Pagecolumn33

[10]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.6039-6042

[11]JournalofMedicinalChemistry,2009,vol.52,p.4650-4656

[12]OrganicandBiomolecularChemistry,2015,vol.13,p.4570-4580

[13]Synthesis,2016,vol.48,p.245-255

[14]JournalofOrganicChemistry,2014,vol.79,p.6708-6714

[15]JournalofOrganicChemistry,2014,vol.79,p.1542-1554

[16]JournalofOrganicChemistry,1997,vol.62,p.6918-6920

[17]JournalofMedicinalChemistry,2008,vol.51,p.4581-4588

[18]Synthesis,1981,vol.No.4,p.266-268

[19]AngewandteChemie-InternationalEdition,2007,vol.46,p.2470-2477

[20]Patent:WO2005/21558,2005,A2.Locationinpatent:Page/Pagecolumn223-224

[21]Patent:US2006/189806,2006,A1.Locationinpatent:Page/Pagecolumn44

[22]OrganicLetters,2004,vol.6,p.213-215

[23]BulletinoftheChemicalSocietyofJapan,1992,vol.65,p.2227-2240

[24]JournaloftheChemicalSociety.Chemicalcommunications,1993,p.1786-1788

[25]Tetrahedron,1994,vol.50,p.9873-9882

[26]BioorganicandMedicinalChemistryLetters,2003,vol.13,p.997-1000

[27]ChemicalandPharmaceuticalBulletin,2005,vol.53,p.1152-1158

Literature

Title: Transport and signaling via the amino acid binding site of the yeast Gap1 amino acid transceptor.

Journal: Nature chemical biology 20090101

Title: Synthesis of a glycosylated peptide thioester by the Boc strategy and its application to segment condensation.

Journal: Bioscience, biotechnology, and biochemistry 20060601

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SDS
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