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52667-89-7,MFCD00184056
Catalog No.:AA00DAZS

52667-89-7 | 1,4,7-Tritosyl-1,4,7-triazonane

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$19.00   $14.00
- +
250mg
97%
in stock  
$25.00   $18.00
- +
1g
97%
in stock  
$74.00   $52.00
- +
  • 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:
AA00DAZS
Chemical Name:
1,4,7-Tritosyl-1,4,7-triazonane
CAS Number:
52667-89-7
Molecular Formula:
C27H33N3O6S3
Molecular Weight:
591.7624
MDL Number:
MFCD00184056
SMILES:
Cc1ccc(cc1)S(=O)(=O)N1CCN(CCN(CC1)S(=O)(=O)c1ccc(cc1)C)S(=O)(=O)c1ccc(cc1)C
Properties
Properties
 
BP:
749.4°C at 760 mmHg  
Form:
Solid  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
948  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
39  
Hydrogen Bond Acceptor Count:
9  
Rotatable Bond Count:
6  
XLogP3:
3.6  

Upstream Synthesis Route

[1]EuropeanJournalofInorganicChemistry,2002,#6,p.1488-1494

[2]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1990,vol.26,#3,p.346-349

[3]KhimiyaGeterotsiklicheskikhSoedinenii,1990,#3,p.401-404

[4]JournaloftheChemicalSociety.PerkinTransactions2,1998,#1,p.83-88

[5]JournaloftheChemicalSociety,DaltonTransactions:InorganicChemistry(1972-1999),2000,#17,p.3034-3040

[6]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2002,vol.41,#2,p.372-375

[7]JournaloftheAmericanChemicalSociety,1980,vol.102,p.6365

[8]BioorganicandMedicinalChemistryLetters,2008,vol.18,#20,p.5364-5367

[9]ChemicalCommunications,2010,vol.46,#10,p.1640-1642

[10]InorganicChemistry,2014,vol.53,#1,p.468-477

[11]EuropeanJournalofInorganicChemistry,2014,#25,p.4084-4092

[12]EuropeanJournalofInorganicChemistry,2014,vol.2014,#25,p.4084-4092

[1]OrganicandBiomolecularChemistry,2018,vol.16,#40,p.7503-7512

[2]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2002,vol.41,#2,p.372-375

[3]JournaloftheAmericanChemicalSociety,2010,vol.132,#49,p.17366-17369

[4]ChemicalCommunications,2010,vol.46,#10,p.1640-1642

[5]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1990,vol.26,#3,p.346-349

[6]KhimiyaGeterotsiklicheskikhSoedinenii,1990,#3,p.401-404

[7]JournaloftheChineseChemicalSociety,2004,vol.51,#5B,p.1201-1208

[8]SyntheticCommunications,2006,vol.36,#11,p.1569-1573

[9]DaltonTransactions,2016,vol.45,#23,p.9412-9418

[10]AustralianJournalofChemistry,1984,vol.37,#5,p.959-970

[11]JournaloftheChemicalSociety.PerkinTransactions2,1998,#1,p.83-88

[12]JournaloftheAmericanChemicalSociety,2012,vol.134,#10,p.4683-4693

[13]Chemistry-AEuropeanJournal,2018,vol.24,#41,p.10434-10442

[1]Patent:US2007/218010,2007,A1,.Locationinpatent:Page/Pagecolumn14;19

[1]JournalofOrganicChemistry,1989,vol.54,#12,p.2990-2992

[2]InorganicChemistry,2014,vol.53,#1,p.468-477

[3]GreenChemistry,2016,vol.18,#20,p.5477-5484

[1]ChemicalCommunications,2007,#18,p.1855-1857

Downstream Synthesis Route

[1]OrganicandBiomolecularChemistry,2018,vol.16,p.7503-7512

[2]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,2002,vol.41,p.372-375

[3]JournaloftheAmericanChemicalSociety,2010,vol.132,p.17366-17369

[4]ChemicalCommunications,2010,vol.46,p.1640-1642

[5]ChemistryofHeterocyclicCompounds,1990,vol.26,p.346-349    KhimiyaGeterotsiklicheskikhSoedinenii,1990,p.401-404

[6]JournaloftheChineseChemicalSociety,2004,vol.51,p.1201-1208

[7]SyntheticCommunications,2006,vol.36,p.1569-1573

[8]DaltonTransactions,2016,vol.45,p.9412-9418

[9]AustralianJournalofChemistry,1984,vol.37,p.959-970

[10]JournaloftheChemicalSociety.PerkinTransactions2(2001),1998,p.83-88

[11]JournaloftheAmericanChemicalSociety,2012,vol.134,p.4683-4693

[12]Chemistry-AEuropeanJournal,2018,vol.24,p.10434-10442

[1]ChemistryLetters,1986,p.369-372

[1]JournaloftheChemicalSociety.Chemicalcommunications,1985,p.918-919

[1]JournalofOrganicChemistry,1989,vol.54,p.2990-2992

[2]InorganicChemistry,2014,vol.53,p.468-477

[3]GreenChemistry,2016,vol.18,p.5477-5484

C7H12N3(1+)*BF4(1-) 
  98-59-9    52667-89-7 

[1]JournaloftheAmericanChemicalSociety,1980,vol.102,p.6365

Literature

Title: Investigation of macrocyclisation routes to 1,4,7-triazacyclononanes: efficient syntheses from 1,2-ditosylamides.

Journal: Organic & biomolecular chemistry 20080121

Title: A new conformer of 1,4,7-tris(p-tolylsulfonyl)-1,4,7-triazacyclononane.

Journal: Acta crystallographica. Section C, Crystal structure communications 20071001

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