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13669-05-1,MFCD00208362
Catalog No.:AA00125H

13669-05-1 | 1,4-Di(2-thienyl)-1,4-butanedione

Pack Size
Purity
Availability
Price(USD)
Quantity
  
250mg
95%
in stock  
$15.00   $11.00
- +
1g
95%
in stock  
$33.00   $23.00
- +
5g
95%
in stock  
$102.00   $71.00
- +
  • 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:
AA00125H
Chemical Name:
1,4-Di(2-thienyl)-1,4-butanedione
CAS Number:
13669-05-1
Molecular Formula:
C12H10O2S2
Molecular Weight:
250.3366
MDL Number:
MFCD00208362
SMILES:
O=C(c1cccs1)CCC(=O)c1cccs1
NSC Number:
671955
Properties
Properties
 
BP:
431°C at 760 mmHg  
Form:
Solid  
MP:
133℃  
Storage:
Inert atmosphere;2-8℃;  

Computed Properties
 
Complexity:
250  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
16  
Hydrogen Bond Acceptor Count:
4  
Rotatable Bond Count:
5  
XLogP3:
2.9  

Upstream Synthesis Route

[1]ChemistryofHeterocyclicCompounds,2011,vol.46,#10,p.1199-1207

[1]ChemistryofHeterocyclicCompounds,2011,vol.46,#10,p.1199-1207

[1]AsianJournalofChemistry,2013,vol.25,#15,p.8772-8774

[2]BioorganicandMedicinalChemistryLetters,1998,vol.8,#19,p.2695-2698

[3]JournalofMaterialsChemistry,2000,vol.10,#1,p.107-114

[4]ElectrochimicaActa,2017,vol.229,p.271-280

[5]JournalofMaterialsChemistry,2011,vol.21,#33,p.12337-12343

[6]NewJournalofChemistry,2018,vol.42,#1,p.450-457

[7]MendeleevCommunications,2009,vol.19,#6,p.329-331

[8]SpectrochimicaActa-PartA:MolecularandBiomolecularSpectroscopy,2016,vol.152,p.8-17

[9]OrganicElectronics:physics,materials,applications,2014,vol.15,#12,p.3735-3745

[10]Synthesis,1991,#6,p.462-464

[11]Tetrahedron,2002,vol.58,#18,p.3467-3472

[12]ChemicalandPharmaceuticalBulletin,2011,vol.59,#10,p.1227-1232

[13]JournalofMaterialsChemistryB,2017,vol.5,#35,p.7384-7392

[14]DaltonTransactions,2018,vol.47,#15,p.5431-5444

[15]ChemistryofHeterocyclicCompounds,2011,vol.46,#10,p.1199-1207

[16]JournalofMaterialsChemistry,2003,vol.13,#5,p.1011-1022

[17]JournalofOrganicChemistry,2005,vol.70,#18,p.7397-7407

[18]TetrahedronLetters,2008,vol.49,#21,p.3530-3533

[19]ChemistryofHeterocyclicCompounds,2008,vol.44,#9,p.1092-1100

[20]JournalofMolecularCatalysisB:Enzymatic,2010,vol.64,#3-4,p.195-199

[21]ElectrochimicaActa,2010,vol.55,#23,p.6933-6940

[22]RussianJournalofAppliedChemistry,2010,vol.83,#8,p.1440-1443

[23]Macromolecules,2011,vol.44,#21,p.8407-8414

[24]Polymer,2011,vol.52,#25,p.5772-5779

[25]ElectrochimicaActa,2012,vol.61,p.50-56

[26]ReactiveandFunctionalPolymers,2013,vol.73,#6,p.847-853

[27]JournalofOrganicChemistry,2013,vol.78,#18,p.9205-9213

[28]Polymer,2013,vol.54,#23,p.6283-6292

[29]DyesandPigments,2015,vol.113,p.121-128

[30]JournalofMaterialsChemistryC,2014,vol.2,#13,p.2431-2438

[31]ElectrochimicaActa,2014,vol.128,p.420-429

[32]Patent:WO2014/101193,2014,A1,.Locationinpatent:Paragraph0106;0107

[33]ElectrochimicaActa,2014,vol.138,p.454-463

[34]ReactiveandFunctionalPolymers,2014,vol.83,p.107-112

[35]ElectrochimicaActa,2014,vol.150,p.245-262

[36]ElectrochimicaActa,2017,vol.228,p.332-342

[37]Patent:CN105085501,2017,B,.Locationinpatent:Paragraph0112-0116

[38]SpectrochimicaActa-PartA:MolecularandBiomolecularSpectroscopy,2014,vol.137,p.1174-1183

[39]Patent:CN105130971,2017,B,.Locationinpatent:Paragraph0120-0126;0136

[40]ReactiveandFunctionalPolymers,2018,vol.131,p.174-180

[1]Synlett,2018,vol.29,#16,p.2195-2198

[1]TetrahedronLetters,2005,vol.46,#41,p.7033-7035

Downstream Synthesis Route

[1]AsianJournalofChemistry,2013,vol.25,p.8772-8774

[2]BioorganicandMedicinalChemistryLetters,1998,vol.8,p.2695-2698

[3]JournalofMaterialsChemistry,2000,vol.10,p.107-114

[4]ElectrochimicaActa,2017,vol.229,p.271-280

[5]JournalofMaterialsChemistry,2011,vol.21,p.12337-12343

[6]NewJournalofChemistry,2018,vol.42,p.450-457

[7]MendeleevCommunications,2009,vol.19,p.329-331

[8]SpectrochimicaActaPartA:MolecularandBiomolecularSpectroscopy,2016,vol.152,p.8-17

[9]Organicelectronics,2014,vol.15,p.3735-3745

[10]Synthesis,1991,p.462-464

[11]Tetrahedron,2002,vol.58,p.3467-3472

[12]ChemicalandPharmaceuticalBulletin,2011,vol.59,p.1227-1232

[13]JournalofMaterialsChemistryB,2017,vol.5,p.7384-7392

[14]DaltonTransactions,2018,vol.47,p.5431-5444

[15]ChemistryofHeterocyclicCompounds,2011,vol.46,p.1199-1207

[16]JournalofMaterialsChemistry,2003,vol.13,p.1011-1022

[17]JournalofOrganicChemistry,2005,vol.70,p.7397-7407

[18]TetrahedronLetters,2008,vol.49,p.3530-3533

[19]ChemistryofHeterocyclicCompounds,2008,vol.44,p.1092-1100

[20]JournalofMolecularCatalysisB:Enzymatic,2010,vol.64,p.195-199

[21]ElectrochimicaActa,2010,vol.55,p.6933-6940

[22]RussianJournalofAppliedChemistry,2010,vol.83,p.1440-1443

[23]Macromolecules,2011,vol.44,p.8407-8414

[24]ElectrochimicaActa,2012,vol.61,p.50-56

[25]Reactiveandfunctionalpolymers,2013,vol.73,p.847-853

[26]JournalofOrganicChemistry,2013,vol.78,p.9205-9213

[27]Polymer,2013,vol.54,p.6283-6292

[28]JournalofMaterialsChemistryC,2014,vol.2,p.2431-2438

[29]ElectrochimicaActa,2014,vol.128,p.420-429

[30]Patent:WO2014/101193,2014,A1.Locationinpatent:Paragraph0106;0107

[31]ElectrochimicaActa,2014,vol.138,p.454-463

[32]Reactiveandfunctionalpolymers,2014,vol.83,p.107-112

[33]ElectrochimicaActa,2014,vol.150,p.245-262

[34]ElectrochimicaActa,2017,vol.228,p.332-342

[35]Patent:CN105085501,2017,B.Locationinpatent:Paragraph0112-0116

[36]SpectrochimicaActaPartA:MolecularandBiomolecularSpectroscopy,2015,vol.137,p.1174-1183

[37]Patent:CN105130971,2017,B.Locationinpatent:Paragraph0120-0126;0136

[38]Reactiveandfunctionalpolymers,2018,vol.131,p.174-180

[1]Synthesis,1991,p.462-464

[2]Synthesis,1991,p.462-464

[1]SyntheticCommunications,1989,vol.19,p.787-792

[1]ChemischeBerichte,1981,vol.114,p.1226-1233

[2]Reactiveandfunctionalpolymers,2012,vol.72,p.533-541

[1]SyntheticCommunications,1984,vol.14,p.1-10

[2]TetrahedronLetters,1999,vol.40,p.8887-8891

Literature

Title: 1,4-Bis(thio-phen-2-yl)butane-1,4-dione.

Journal: Acta crystallographica. Section E, Structure reports online 20120301

Title: Microsphere-based protease assays and screening application for lethal factor and factor Xa.

Journal: Cytometry. Part A : the journal of the International Society for Analytical Cytology 20060501

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SDS
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