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Home Other Building Blocks 76387-70-7
76387-70-7,MFCD01632072
Catalog No.:AA0035W4

76387-70-7 | Boc-D-Dap-OH

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$6.00   $4.00
- +
250mg
97%
in stock  
$7.00   $5.00
- +
1g
95%
in stock  
$9.00   $6.00
- +
5g
95%
in stock  
$18.00   $13.00
- +
10g
95%
in stock  
$29.00   $20.00
- +
25g
97%
in stock  
$57.00   $40.00
- +
100g
97%
in stock  
$227.00   $159.00
- +
  • 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:
AA0035W4
Chemical Name:
Boc-D-Dap-OH
CAS Number:
76387-70-7
Molecular Formula:
C8H16N2O4
Molecular Weight:
204.2236
MDL Number:
MFCD01632072
SMILES:
NC[C@H](C(=O)O)NC(=O)OC(C)(C)C
Properties
Properties
 
Form:
Solid  
MP:
200-203℃  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
222  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
5  
XLogP3:
-2.7  

Upstream Synthesis Route

[1]BioorganicandMedicinalChemistryLetters,2006,vol.16,#23,p.6039-6042

[2]JournalofMedicinalChemistry,2008,vol.51,#15,p.4581-4588

[3]JournalofMedicinalChemistry,2009,vol.52,#15,p.4650-4656

[4]Patent:WO2005/21558,2005,A2,.Locationinpatent:Page/Pagecolumn224

[5]OrganicandBiomolecularChemistry,2015,vol.13,#6,p.1629-1633

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

[7]JournalofOrganicChemistry,2012,vol.77,#13,p.5696-5704

[8]OrganicandBiomolecularChemistry,2015,vol.13,#15,p.4570-4580

[9]Patent:WO2006/123020,2006,A1,.Locationinpatent:Page/Pagecolumn37

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

[11]ChemicalCommunications,2011,vol.47,#4,p.1198-1200

[12]Patent:WO2013/52394,2013,A1,.Locationinpatent:Paragraph00292

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

[1]ChemicalandPharmaceuticalBulletin,2005,vol.53,#9,p.1152-1158

[1]OrganicandBiomolecularChemistry,2015,vol.13,#6,p.1629-1633

[2]ChemicalCommunications,2011,vol.47,#4,p.1198-1200

[3]JournalofOrganicChemistry,2012,vol.77,#13,p.5696-5704

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

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

[6]BioorganicandMedicinalChemistry,1999,vol.7,#1,p.161-175

[7]OrganicLetters,2007,vol.9,#1,p.25-28

[8]BioorganicandMedicinalChemistryLetters,2006,vol.16,#23,p.6039-6042

[9]JournalofMedicinalChemistry,2009,vol.52,#15,p.4650-4656

[10]OrganicandBiomolecularChemistry,2015,vol.13,#15,p.4570-4580

[11]Synthesis(Germany),2016,vol.48,#2,p.245-255

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

[13]JournalofOrganicChemistry,2014,vol.79,#4,p.1542-1554

[14]JournalofOrganicChemistry,1997,vol.62,#20,p.6918-6920

[15]JournalofMedicinalChemistry,2008,vol.51,#15,p.4581-4588

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

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

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

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

[20]OrganicLetters,2004,vol.6,#2,p.213-215

[21]BulletinoftheChemicalSocietyofJapan,1992,vol.65,#8,p.2227-2240

[22]JournaloftheChemicalSociety,ChemicalCommunications,1993,#23,p.1786-1788

[23]Tetrahedron,1994,vol.50,#33,p.9873-9882

[24]BioorganicandMedicinalChemistryLetters,2003,vol.13,#6,p.997-1000

[25]ChemicalandPharmaceuticalBulletin,2005,vol.53,#9,p.1152-1158

[1]JournaloftheAmericanChemicalSociety,1985,vol.107,#24,p.7105-7109

Downstream Synthesis Route
108-97-4    76387-70-7   
N-(tert-butoxycarbonyl)-L-3-deoxymimosine 

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

[1]JournalofMedicinalChemistry,1990,vol.33,p.2755-2759

55750-49-7    76387-70-7   
(S)-2-tert-Butoxycarbonylamino-3-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-propionicacid 

[1]PolishJournalofChemistry,1993,vol.67,p.673-683

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

[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
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