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3392-05-0,MFCD00065974
Catalog No.:AA003UDN

3392-05-0 | Boc-Ala-OSu

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
95%
in stock  
$14.00   $10.00
- +
25g
95%
in stock  
$52.00   $36.00
- +
100g
95%
in stock  
$195.00   $137.00
- +
  • 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:
AA003UDN
Chemical Name:
Boc-Ala-OSu
CAS Number:
3392-05-0
Molecular Formula:
C12H18N2O6
Molecular Weight:
286.2811
MDL Number:
MFCD00065974
SMILES:
C[C@@H](C(=O)ON1C(=O)CCC1=O)NC(=O)OC(C)(C)C
Properties
Properties
 
Form:
Solid  
MP:
161-163 °C  
Stability:
Moisture Sensitive  
Storage:
Inert atmosphere;-20 ℃;  

Computed Properties
 
Complexity:
424  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
20  
Hydrogen Bond Acceptor Count:
6  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
6  
XLogP3:
0.4  

Upstream Synthesis Route

[1]JournalofPharmaceuticalSciences,1987,vol.76,#2,p.134-140

[2]Chemicalandpharmaceuticalbulletin,2002,vol.50,#2,p.239-252

[3]JournaloftheChemicalSociety,ChemicalCommunications,1985,#8,p.473

[4]CarbohydrateResearch,1984,vol.132,p.275-286

[5]JournaloftheAmericanChemicalSociety,1992,vol.114,#17,p.6653-6661

[6]JournaloftheAmericanChemicalSociety,1996,vol.118,#29,p.6975-6985

[7]JournalofMedicinalChemistry,1997,vol.40,#15,p.2386-2397

[8]ChemistryofNaturalCompounds,1997,vol.33,#5,p.568-570

[9]ChemistryofNaturalCompounds,1998,vol.34,#1,p.78-79

[10]JournalofMedicinalChemistry,2003,vol.46,#21,p.4543-4551

[11]Patent:EP2123283,2009,A1,.Locationinpatent:Page/Pagecolumn17-18

[12]Patent:US2009/325894,2009,A1,.Locationinpatent:Page/Pagecolumn11-12

[13]BioorganicandMedicinalChemistryLetters,2009,vol.19,#12,p.3220-3224

[14]Biomacromolecules,2010,vol.11,#2,p.496-504

[15]OrganicandBiomolecularChemistry,2011,vol.9,#11,p.4182-4187

[16]Synlett,2012,#1,p.142-144

[17]ChineseChemicalLetters,2011,vol.22,#12,p.1443-1446

[18]Biochimie,2013,vol.95,#6,p.1120-1126

[19]ChineseChemicalLetters,2016,vol.27,#3,p.357-360

[20]Patent:EP2612857,2017,B1,.Locationinpatent:Paragraph0137

[21]JournalofMolecularBiology,2018,vol.430,#6,p.842-852

[1]JournalofOrganicChemistry,1987,vol.52,#12,p.2364-2367

[2]Patent:US4782164,1988,A,

[1]TetrahedronLetters,2002,vol.43,#9,p.1661-1664

[1]BulletinoftheAcademyofSciencesoftheUSSR,DivisionofChemicalScience(EnglishTranslation),1984,vol.33,p.1067-1070

[2]IzvestiyaAkademiiNaukSSSR,SeriyaKhimicheskaya,1984,#5,p.1163-1165

[1]CollectionofCzechoslovakChemicalCommunications,2005,vol.70,#10,p.1615-1641

Downstream Synthesis Route

[1]ChemicalandPharmaceuticalBulletin,1991,vol.39,p.2647-2652

[2]JournaloftheChemicalSociety.PerkintransactionsI,1972,vol.14,p.1809-1814

[1]Berges;DeWolfJr.;Dunn;Grappel;Newman;Taggart;Gilvarg[JournalofMedicinalChemistry,1986,vol.29,#1,p.89-95]

[1]AustralianJournalofChemistry,1983,vol.36,p.751-758

10466-56-5    3392-05-0   
(S)-1-((1S,2S)-1-Carbamoyl-2-methyl-butylcarbamoyl)-ethyl-carbamicacidtert-butylester 

[1]Tetrahedron,1986,vol.42,p.829-834

[1]ChemicalandPharmaceuticalBulletin,1981,vol.29,p.2215-2221

Literature
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SDS
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