Name: Name:1,4,7-Tritosyl-1,4,7-triazonane
Brand: AABLOCKS
SKU: AA00DAZS
Rating: 90 (10 reviews)

Catalog No.: AA00DAZS

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

Pack Size： 100mg

Purity： 97%

in stock

$20.00 $14.00

Pack Size： 250mg

Purity： 97%

in stock

$25.00 $18.00

Pack Size： 1g

Purity： 97%

in stock

$75.00 $53.00

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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

BP: 749.4°C at 760 mmHg

Form: Solid

Storage: Keep in dry area;Room Temperature;

Complexity: 948

Covalently-Bonded Unit Count: 1

Defined Atom Stereocenter Count: 0

Defined Bond Stereocenter Count: 0

Formal Charge: 0

Heavy Atom Count: 39

Hydrogen Bond Acceptor Count: 9

Hydrogen Bond Donor Count: 0

Isotope Atom Count: 0

Rotatable Bond Count: 6

Undefined Atom Stereocenter Count: 0

Undefined Bond Stereocenter Count: 0

XLogP3: 3.6

Upstream Synthesis Route

52667-89-7

4730-54-5

[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

56187-04-3

6315-52-2

52667-89-7

[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

6315-52-2

52601-80-6

52667-89-7

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

56187-04-3

106-93-4

52667-89-7

[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

111-40-0

98-59-9

52667-89-7

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

Downstream Synthesis Route

56187-04-3

6315-52-2

52667-89-7

[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

1074-82-4

99142-40-2

67455-96-3

52667-89-7

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

99142-40-2

52667-89-7

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

56187-04-3

106-93-4

52667-89-7

[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 fold

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

Journal: Organic & biomolecular chemistry20080121

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

Journal: Acta crystallographica. Section C, Crystal structure communications20071001

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