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Home Deuterated Building Blocks 19728-63-3
19728-63-3,MFCD00065948
Catalog No.:AA002AMR

19728-63-3 | Z-Thr-oh

Pack Size
Purity
Availability
Price(USD)
Quantity
  
10g
96%
in stock  
$21.00   $15.00
- +
25g
96%
in stock  
$39.00   $28.00
- +
100g
96%
in stock  
$113.00   $79.00
- +
500g
96%
in stock  
$469.00   $328.00
- +
  • 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:
AA002AMR
Chemical Name:
Z-Thr-oh
CAS Number:
19728-63-3
Molecular Formula:
C12H15NO5
Molecular Weight:
253.2512
MDL Number:
MFCD00065948
SMILES:
O=C(N[C@H](C(=O)O)[C@H](O)C)OCc1ccccc1
Properties
Computed Properties
 
Complexity:
288  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
5  
Hydrogen Bond Donor Count:
3  
Rotatable Bond Count:
6  
XLogP3:
0.8  

Upstream Synthesis Route

[1]Synlett,2018,vol.29,#11,p.1430-1436

[1]JournaloftheAmericanChemicalSociety,1987,vol.109,#17,p.5167-5175

[2]Tetrahedron,2000,vol.56,#29,p.5077-5083

[3]OrganicLetters,2005,vol.7,#22,p.5047-5050

[4]Tetrahedron,2007,vol.63,#35,p.8645-8657

[5]ChemicalCommunications,2014,vol.50,#88,p.13608-13611

[6]CanadianJournalofChemistry,1962,vol.40,p.2229-2233

[7]BulletinoftheChemicalSocietyofJapan,1978,vol.51,#6,p.1897-1898

[8]OrganicLetters,2010,vol.12,#7,p.1624-1627

[9]JournaloftheAmericanChemicalSociety,2011,vol.133,#1,p.102-107

[1]Tetrahedron,1987,vol.43,#22,p.5341-5349

[2]JustusLiebigsAnnalenderChemie,1977,p.806-810

[3]Tetrahedron,1998,vol.54,#35,p.10265-10274

[1]RecueildesTravauxChimiquesdesPays-Bas,1962,vol.81,p.691-698

[2]ProceedingsoftheChemicalSociety,London,1961,p.249

[3]JournaloftheAmericanChemicalSociety,1963,vol.85,p.201-207

[1]ChemischeBerichte,1964,vol.97,p.2490-2496

Downstream Synthesis Route

[1]Tetrahedron,1987,vol.43,p.5341-5349

[2]JustusLiebigsAnnalenderChemie,1977,p.806-810

[3]Tetrahedron,1998,vol.54,p.10265-10274

[1]JournaloftheAmericanChemicalSociety,1987,vol.109,p.5167-5175

[2]Tetrahedron,2000,vol.56,p.5077-5083

[3]OrganicLetters,2005,vol.7,p.5047-5050

[4]ChemicalCommunications,2014,vol.50,p.13608-13611

[5]CanadianJournalofChemistry,1962,vol.40,p.2229-2233

[6]BulletinoftheChemicalSocietyofJapan,1978,vol.51,p.1897-1898

[7]OrganicLetters,2010,vol.12,p.1624-1627

[8]JournaloftheAmericanChemicalSociety,2011,vol.133,p.102-107

[1]EuropeanJournalofMedicinalChemistry,1982,vol.17,p.515-520

[2]JournalofgeneralchemistryoftheUSSR,1970,vol.40,p.395-407    ZhurnalObshcheiKhimii,1970,vol.40,p.429-443

[3]ChemicalandPharmaceuticalBulletin,1974,vol.22,p.859-863

[4]TetrahedronLetters,1991,vol.32,p.255-258

[1]HelveticaChimicaActa,1994,vol.77,p.1313-1330

[2]JournalofOrganicChemistry,1983,vol.48,p.2557-2563

[3]Chemicalandpharmaceuticalbulletin,1967,vol.15,p.707-710

19728-63-3    66-84-2   
N-(N-Carbobenzoxy-L-threonyl)-D-glucosamin 

[1]CanadianJournalofChemistry,1962,vol.40,p.2229-2233

Literature

Title: De novo synthesis of a 2-acetamido-4-amino-2,4,6-trideoxy-D-galactose (AAT) building block for the preparation of a Bacteroides fragilis A1 polysaccharide fragment.

Journal: Organic letters 20100402

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SDS
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