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77449-94-6,MFCD09749867
Catalog No.:AA003OWK

77449-94-6 | Cis-4-Hydroxy-D-proline, HCl

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5g
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$9.00   $7.00
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10g
95%
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$16.00   $11.00
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25g
95%
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$26.00   $18.00
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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:
AA003OWK
Chemical Name:
Cis-4-Hydroxy-D-proline, HCl
CAS Number:
77449-94-6
Molecular Formula:
C5H10ClNO3
Molecular Weight:
167.5908
MDL Number:
MFCD09749867
SMILES:
O[C@H]1CN[C@H](C1)C(=O)O.Cl
Properties
Properties
 
BP:
368.6°C at 760 mmHg  
Form:
Solid  
MP:
114-116℃  
Storage:
Inert atmosphere;Room Temperature;  

Computed Properties
 
Complexity:
125  
Covalently-Bonded Unit Count:
2  
Defined Atom Stereocenter Count:
2  
Heavy Atom Count:
10  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
4  
Rotatable Bond Count:
1  

Upstream Synthesis Route

[1]JournalofOrganicChemistry,2009,vol.74,#2,p.513-519

[2]BioorganicandMedicinalChemistryLetters,2016,vol.26,#10,p.2434-2437

[3]JournaloftheAmericanChemicalSociety,2013,vol.135,#11,p.4333-4363

[4]Patent:US2009/163472,2009,A1,.Locationinpatent:Page/Pagecolumn21

[5]JournalofHeterocyclicChemistry,2011,vol.48,#5,p.1132-1139

[6]JournalofOrganicChemistry,2010,vol.75,#5,p.1620-1629

[7]BioorganicandMedicinalChemistryLetters,2006,vol.16,#15,p.4099-4101

[8]Patent:WO2010/104721,2010,A1,.Locationinpatent:Page/Pagecolumn21

[9]JournalofOrganicChemistry,1981,vol.46,#14,p.2954-2960

[10]JournalofOrganicChemistry,1994,vol.59,#13,p.3616-3625

[11]JournaloftheChemicalSociety-PerkinTransactions1,1997,#4,p.539-546

[12]Patent:WO2014/32,2014,A1,

[1]Patent:WO2014/32,2014,A1,.Locationinpatent:Page/Pagecolumn64

[1]BioorganicandMedicinalChemistryLetters,2009,vol.19,#1,p.21-26

[1]JournalofMedicinalChemistry,2018,vol.61,#3,p.681-694

[2]JournaloftheAmericanChemicalSociety,2013,vol.135,#11,p.4333-4363

[3]TetrahedronAsymmetry,2015,vol.26,#20,p.1156-1166

[4]Patent:TW2017/8221,2017,A,.Locationinpatent:Page/Pagecolumn92;93

[1]Patent:TW2017/8221,2017,A,.Locationinpatent:Page/Pagecolumn41

[2]JournalofOrganicChemistry,2009,vol.74,#2,p.513-519

[3]Patent:US2009/163472,2009,A1,.Locationinpatent:Page/Pagecolumn21

[4]Patent:WO2014/32,2014,A1,.Locationinpatent:Page/Pagecolumn64

[5]BioorganicandMedicinalChemistryLetters,2016,vol.26,#10,p.2434-2437

Downstream Synthesis Route

[1]JournalofMedicinalChemistry,2017,vol.60,p.3913-3932

[2]JournalofOrganicChemistry,1981,vol.46,p.2954-2960

[3]ChemicalandPharmaceuticalBulletin,1999,vol.47,p.1650-1654

[4]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.4099-4101

[5]TetrahedronAsymmetry,1995,vol.6,p.1641-1656

[1]JournalofOrganicChemistry,1994,vol.59,p.3616-3625

[1]Synthesis,1990,vol.1,p.925-930

77449-94-6   
4-(6-amino-purin-9-yl)-2-hydroxymethyl-pyrrolidin-1-ol 

[1]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.4099-4101

77449-94-6   
N-(2-cyanoethyl)-cis-4-(6-amino-9H-purin-9-yl)-D-prolinol 

[1]BioorganicandMedicinalChemistryLetters,2006,vol.16,p.4099-4101

Literature
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