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87694-52-8,MFCD00151897
Catalog No.:AA00GSME

87694-52-8 | Boc-val-n(och3)ch3

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
95%
in stock  
$35.00   $25.00
- +
5g
95%
in stock  
$70.00   $49.00
- +
25g
95%
in stock  
$92.00   $64.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00GSME
Chemical Name:
Boc-val-n(och3)ch3
CAS Number:
87694-52-8
Molecular Formula:
C12H24N2O4
Molecular Weight:
260.3300
MDL Number:
MFCD00151897
SMILES:
CON(C(=O)[C@H](C(C)C)NC(=O)OC(C)(C)C)C
Properties
Computed Properties
 
Complexity:
297  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
18  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
6  
XLogP3:
1.9  

Downstream Synthesis Route

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[2]JournalofOrganicChemistry,2009,vol.74,p.5614-5617

[3]Journaloflabelledcompoundsandradiopharmaceuticals,2014,vol.57,p.275-278

[4]OrganicLetters,2016,vol.18,p.2312-2315

[5]JournalofMedicinalChemistry,1992,vol.35,p.4795-4808

[6]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.1672-1683

[7]EuropeanJournalofOrganicChemistry,2014,vol.2014,p.1672-1683

[8]JournalofMedicinalChemistry,1994,vol.37,p.4538-4553

[9]Tetrahedron,1990,vol.46,p.2807-2816

[10]OrganicLetters,2011,vol.13,p.980-983

[11]AngewandteChemie-InternationalEdition,2013,vol.52,p.8957-8960    Angew.Chem.,2013,vol.125,p.9126-9129,4

[12]HelveticaChimicaActa,1998,vol.81,p.983-1002

[13]JournalofOrganicChemistry,2005,vol.70,p.9940-9946

[14]Synlett,2001,p.299-301

[15]BioorganicandMedicinalChemistryLetters,2014,vol.24,p.2244-2246

[16]Tetrahedron,2002,vol.58,p.9445-9458

[17]Synthesis,1983,p.676-678

[18]AngewandteChemie-InternationalEdition,2016,vol.55,p.5842-5845    Angew.Chem.,2016,vol.128,p.5936-5939,4

[19]Patent:WO2009/26197,2009,A1.Locationinpatent:Page/Pagecolumn92

[20]JournalofAntibiotics,2002,vol.55,p.322-336

[21]JournalofMedicinalChemistry,2005,vol.48,p.6767-6771

[22]JournalofMedicinalChemistry,1992,vol.35,p.3949-3955

[23]TetrahedronLetters,1992,vol.33,p.3265-3268

[24]TetrahedronLetters,1998,vol.39,p.6593-6596

[25]OrganicLetters,2006,vol.8,p.5357-5360

[26]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.1102-1106

[27]JournalofNaturalProducts,2003,vol.66,p.183-199

[28]JournalofMedicinalChemistry,2000,vol.43,p.3434-3442

[29]OrganicLetters,2010,vol.12,p.3453-3455

[30]OrganicandBiomolecularChemistry,2010,vol.8,p.4855-4860

[31]OrganicandBiomolecularChemistry,2011,vol.9,p.6566-6574

[32]TetrahedronLetters,2012,vol.53,p.1313-1315

[33]Patent:EP3459941,2019,A1.Locationinpatent:Paragraph0282

[34]TetrahedronLetters,2002,vol.43,p.7389-7392

[1]TetrahedronLetters,1994,vol.35,p.3183-3186

[2]JournalofMedicinalChemistry,2009,vol.52,p.3679-3688

[3]JournalofOrganicChemistry,2011,vol.76,p.6209-6217

[1]JournalofMedicinalChemistry,1994,vol.37,p.4538-4553

[2]TetrahedronLetters,1992,vol.33,p.3265-3268

[1]Tetrahedron,1990,vol.46,p.2807-2816

[1]JournalofMedicinalChemistry,1992,vol.35,p.4284-4296

Literature
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SDS
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