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56074-20-5,MFCD04633145
Catalog No.:AA00D8DC

56074-20-5 | Boc-iminodiacetic acid

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
97%
in stock  
$7.00   $5.00
- +
25g
95%
in stock  
$17.00   $12.00
- +
  • 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:
AA00D8DC
Chemical Name:
Boc-iminodiacetic acid
CAS Number:
56074-20-5
Molecular Formula:
C9H15NO6
Molecular Weight:
233.2185
MDL Number:
MFCD04633145
SMILES:
O=C(N(CC(=O)O)CC(=O)O)OC(C)(C)C
Properties
Properties
 
BP:
412°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;2-8℃;  

Computed Properties
 
Complexity:
277  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
6  
XLogP3:
0.3  

Upstream Synthesis Route

[1]JournalofMedicinalChemistry,1996,vol.39,#8,p.1601-1608

[2]Patent:WO2004/35576,2004,A2,.Locationinpatent:Page170

[3]Patent:WO2005/117904,2005,A2,.Locationinpatent:Page/Pagecolumn404-405

[4]Tetrahedron,1996,vol.52,#29,p.9793-9804

[5]BioorganicandMedicinalChemistry,1998,vol.6,#8,p.1347-1378

[6]Pharmazie,2001,vol.56,#1,p.58-60

[7]TetrahedronLetters,1994,vol.35,#12,p.1863-1866

[8]EuropeanJournalofMedicinalChemistry,2015,vol.90,p.547-567

[9]BioorganicandMedicinalChemistry,2001,vol.9,#4,p.837-846

[10]OrganicLetters,2015,vol.17,#15,p.3930-3933

[11]Patent:WO2007/108566,2007,A1,.Locationinpatent:Page/Pagecolumn7;9-10

[12]Patent:EP1443046,2004,A1,.Locationinpatent:Page42

[13]BioorganicandMedicinalChemistryLetters,2017,vol.27,#4,p.708-712

[14]Patent:CN106631879,2017,A,.Locationinpatent:Paragraph0025-0027

[1]TetrahedronLetters,1986,vol.27,#15,p.1685-1686

[2]Tetrahedron,1992,vol.48,#8,p.1407-1416

[1]Patent:US6395266,2002,B1,

[1]Patent:US6153655,2000,A,

[1]BulletinoftheChemicalSocietyofJapan,1989,vol.62,#7,p.2404-2406

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,1996,vol.39,p.1601-1608

[2]Patent:WO2004/35576,2004,A2.Locationinpatent:Page170

[3]Patent:WO2005/117904,2005,A2.Locationinpatent:Page/Pagecolumn404-405

[4]Tetrahedron,1996,vol.52,p.9793-9804

[5]BioorganicandMedicinalChemistry,1998,vol.6,p.1347-1378

[6]Pharmazie,2001,vol.56,p.58-60

[7]TetrahedronLetters,1994,vol.35,p.1863-1866

[8]EuropeanJournalofMedicinalChemistry,2015,vol.90,p.547-567

[9]BioorganicandMedicinalChemistry,2001,vol.9,p.837-846

[10]OrganicLetters,2015,vol.17,p.3930-3933

[11]Patent:WO2007/108566,2007,A1.Locationinpatent:Page/Pagecolumn7;9-10

[12]Patent:EP1443046,2004,A1.Locationinpatent:Page42

[13]BioorganicandMedicinalChemistryLetters,2017,vol.27,p.708-712

[14]Patent:CN106631879,2017,A.Locationinpatent:Paragraph0025-0027

5250-72-6    56074-20-5   
{<i>tert</i>-butoxycarbonyl-(2,3-dichloro-4,6-disulfamoyl-phenylcarbamoyl)-methyl-amino}-aceticacid 

[1]Scozzafava,Andrea;Menabuoni,Luca;Mincione,Francesco;Supuran,ClaudiuT.[JournalofMedicinalChemistry,2002,vol.45,#7,p.1466-1476]

53297-68-0    56074-20-5   
{<i>tert</i>-butoxycarbonyl-(2-chloro-4-sulfamoyl-phenylcarbamoyl)-methyl-amino}-aceticacid 

[1]JournalofMedicinalChemistry,2002,vol.45,p.1466-1476

56074-20-5    21950-36-7   
5'-N-carboxymethyl-(N-tert-butyloxycarbonyl)acetamido-5'-deoxy-2',3'-O-isopropylidene-adenosine 

[1]Enkvist,Erki;Lavogina,Darja;Raidaru,Gerda;Vaasa,Angela;Viil,Indrek;Lust,Marje;Viht,Kaido;Uri,Asko[JournalofMedicinalChemistry,2006,vol.49,#24,p.7150-7159]

[1]Patent:WO2007/108566,2007,A1.Locationinpatent:Page/Pagecolumn7-8

Literature

Title: Computer applications for prediction of protein-protein interactions and rational drug design.

Journal: Advances and applications in bioinformatics and chemistry : AABC 20090101

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