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17193-39-4,MFCD00153486
Catalog No.:AA0038XK

17193-39-4 | H-L-Cha-OMe HCl

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1g
97%
in stock  
$29.00   $20.00
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5g
97%
in stock  
$36.00   $25.00
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10g
97%
in stock  
$44.00   $31.00
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25g
97%
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$89.00   $62.00
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100g
97%
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$336.00   $235.00
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  • 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:
AA0038XK
Chemical Name:
H-L-Cha-OMe HCl
CAS Number:
17193-39-4
Molecular Formula:
C10H20ClNO2
Molecular Weight:
221.7243
MDL Number:
MFCD00153486
SMILES:
COC(=O)[C@@H](NC1CCCCC1)C.Cl
Properties
Computed Properties
 
Complexity:
164  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
2  
Rotatable Bond Count:
4  

Upstream Synthesis Route

[1]Synthesis,2009,#14,p.2440-2446

[2]JournalofMedicinalChemistry,1994,vol.37,#7,p.913-923

[1]EuropeanJournalofMedicinalChemistry,2013,vol.68,p.253-259

[1]AdvancedSynthesisandCatalysis,2001,vol.343,#8,p.802-808

[1]OrganicProcessResearchandDevelopment,2003,vol.7,#2,p.164-167

[1]TetrahedronAsymmetry,2004,vol.15,#13,p.2067-2073

[2]JournalofOrganicChemistry,1995,vol.60,#24,p.8074-8080

[3]JournalofOrganicChemistry,1997,vol.62,#20,p.6862-6869

[4]JournalofMedicinalChemistry,2015,vol.58,#7,p.3144-3155

[5]Chemistry-AEuropeanJournal,2015,vol.21,#28,p.10031-10038

Downstream Synthesis Route

[1]JournaloftheChemicalSociety.PerkintransactionsI,1968,vol.5,p.531-540

[1]JournalofMedicinalChemistry,1994,vol.37,p.913-923

[2]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.1975-1980

32315-10-9    17193-39-4   
(S)-3-Cyclohexyl-2-trichloromethoxycarbonylamino-propionicacidmethylester 

[1]JournalofMedicinalChemistry,1993,vol.36,p.468-478

[1]TetrahedronAsymmetry,2004,vol.15,p.2067-2073

[2]JournalofOrganicChemistry,1995,vol.60,p.8074-8080

[3]JournalofOrganicChemistry,1997,vol.62,p.6862-6869

[4]JournalofMedicinalChemistry,2015,vol.58,p.3144-3155

[5]Chemistry-AEuropeanJournal,2015,vol.21,p.10031-10038

(benzyl)Phe-olhydrochloride 
  75-44-5    17193-39-4   
retro-Cha-OMeΨNHCONH-4-(benzyl)-phenylalaninealcohol 

[1]Organicletters,2001,vol.3,p.2313-2316

Literature
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SDS
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