3958-03-0,MFCD00005419
Catalog No.:AA0035KV

3958-03-0 | Tetrabromothiophene

Pack Size
Purity
Availability
Price(USD)
Quantity
  
5g
98%
in stock  
$12.00   $8.00
- +
25g
98%
in stock  
$43.00   $30.00
- +
100g
98%
in stock  
$110.00   $77.00
- +
500g
98%
in stock  
$504.00 $353.00
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
Technical Information
Catalog Number:
AA0035KV
Chemical Name:
Tetrabromothiophene
CAS Number:
3958-03-0
Molecular Formula:
C4Br4S
Molecular Weight:
399.7238
MDL Number:
MFCD00005419
SMILES:
Brc1sc(c(c1Br)Br)Br
NSC Number:
65427
Properties
Properties
 
BP:
326°C at 760 mmHg  
Form:
Solid  
MP:
116-118 °C(lit.);  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
96.7  
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0  
Defined Bond Stereocenter Count:
0  
Formal Charge:
0  
Heavy Atom Count:
9  
Hydrogen Bond Acceptor Count:
1  
Hydrogen Bond Donor Count:
0  
Isotope Atom Count:
0  
Rotatable Bond Count:
0  
Undefined Atom Stereocenter Count:
0  
Undefined Bond Stereocenter Count:
0  
XLogP3:
5  

Upstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,1953,vol.75,p.1764,1767

[1]JournaloftheAmericanChemicalSociety,1953,vol.75,p.1764,1767

[1]ArkivfoerKemi,1957,vol.11,p.373,379,380

[1]Patent:WO2004/58763,2004,A1,.Locationinpatent:Page41-42

[1]JournalofOrganicChemistry,2008,vol.73,#1,p.323-326

[2]Synthesis,1990,#5,p.403-405

[3]Synthesis,1990,#5,p.403-405

[4]Chemistry-AEuropeanJournal,2004,vol.10,#13,p.3331-3340

[5]TetrahedronLetters,2004,vol.45,#17,p.3405-3407

[6]Patent:WO2004/58702,2004,A2,.Locationinpatent:Page32;24

[7]CanadianJournalofChemistry,1985,vol.63,p.2669-2672

[8]Patent:US2016/264595,2016,A1,.Locationinpatent:Paragraph0058;0060

[9]JournaloftheAmericanChemicalSociety,2007,vol.129,#26,p.8310-8319

[10]JournalofMaterialsChemistry,1999,vol.9,#8,p.1719-1725

[11]JournalofMaterialsChemistry,2012,vol.22,#1,p.100-108

[12]JournalofMolecularStructure,2000,vol.521,#1-3,p.285-301

[13]JournalofOrganicChemistry,1997,vol.62,#7,p.1940-1954

[14]ElectrochimicaActa,2010,vol.56,#1,p.326-332

[15]ActaChemicaScandinavica(1947-1973),1959,vol.13,p.1045

[16]ArkivfoerKemi,1957,vol.11,p.317,322

[17]JustusLiebigsAnnalenderChemie,1934,vol.512,p.136,156

[18]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1993,vol.29,#8,p.889-891

[19]KhimiyaGeterotsiklicheskikhSoedinenii,1993,#8,p.1046-1048

[20]ChemistryLetters,2003,vol.32,#8,p.744-745

[21]JournalofMaterialsChemistry,2012,vol.22,#11,p.4944-4952

[22]OrganicLetters,2012,vol.14,#19,p.5058-5061

[23]JournalofPolymerScience,PartA:PolymerChemistry,2017,vol.55,#16,p.2629-2638

Downstream Synthesis Route

[1]TetrahedronLetters,2004,vol.45,p.3405-3407

[2]Chemistry-AEuropeanJournal,2004,vol.10,p.3331-3340

[3]JournalofMaterialsChemistryA,2020,vol.8,p.5315-5322

[4]JournaloftheAmericanChemicalSociety,2007,vol.129,p.8310-8319

[5]JournalofOrganicChemistry,2008,vol.73,p.323-326

[6]ElectrochimicaActa,2010,vol.56,p.326-332

[7]JournalofMaterialsChemistry,2012,vol.22,p.100-108

[8]Patent:US2016/264595,2016,A1.Locationinpatent:Paragraph0058;0059

[9]MolecularCrystalsandLiquidCrystals,2010,vol.524,p.17-25

[10]Patent:KR2015/39459,2015,A.Locationinpatent:Paragraph0197-0204

[11]JournalofMolecularStructure,2000,vol.521,p.285-301

[12]Tetrahedron,2017,vol.73,p.5847-5852

[13]Patent:KR101791161,2017,B1.Locationinpatent:Paragraph0204-0210

[14]Patent:WO2004/58702,2004,A2.Locationinpatent:Page31-32;24

[15]Patent:WO2004/58763,2004,A1.Locationinpatent:Page41-42

[16]BulletinoftheChemicalSocietyofJapan,1991,vol.64,p.2566-2568

[17]JournalofOrganicChemistry,1997,vol.62,p.1940-1954

[18]JournalofMaterialsChemistry,1999,vol.9,p.1719-1725

[19]JustusLiebigsAnnalenderChemie,1934,vol.512,p.136,156

[20]ChemischeBerichte,1883,vol.16,p.2172

[21]ChemistryLetters,2003,vol.32,p.744-745

[22]Molecules,2009,vol.14,p.1013-1031

[23]InorganicChemistry,2011,vol.50,p.10623-10632

[24]JournalofMaterialsChemistry,2012,vol.22,p.4944-4952

[25]AdvancedSynthesisandCatalysis,2012,vol.354,p.1819-1826

[26]ChemicalCommunications,2014,vol.50,p.15183-15186

[27]Macromolecules,2019,vol.52,p.6523-6532

[1]ChemischeBerichte,1894,vol.27,p.2837

[1]ChemischeBerichte,1893,vol.26,p.2458

[1]ChemischeBerichte,1893,vol.26,p.2458

[1]SyntheticCommunications,1990,vol.20,p.2119-2122

Literature

Title: Efficient synthesis of thieno[3,2-b:4,5-b']diindoles and benzothieno[3,2-b]indoles by Pd-catalyzed site-selective C-C and C-N coupling reactions.

Journal: Organic & biomolecular chemistry 20121207

Title: Selective mono- to perarylations of tetrabromothiophene by a cyclobutene-1,2-diylbisimidazolium preligand.

Journal: The Journal of organic chemistry 20110916

Title: 2,3,4-Tribromo-thio-phene.

Journal: Acta crystallographica. Section E, Structure reports online 20080401

Title: Structures of tetrabromothiophene and tetrabromoselenophene: the influence of the heteroatom on the heterophene packing.

Journal: Acta crystallographica. Section B, Structural science 20071001

Quotation Request
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Additional Info:
SDS
Tags:3958-03-0 Molecular Formula|3958-03-0 MDL|3958-03-0 SMILES|3958-03-0 Tetrabromothiophene
Catalog No.: AA0035KV
3958-03-0,MFCD00005419
3958-03-0 | Tetrabromothiophene
Pack Size: 5g
Purity: 98%
in stock
$12.00 $8.00
Pack Size: 25g
Purity: 98%
in stock
$43.00 $30.00
Pack Size: 100g
Purity: 98%
in stock
$110.00 $77.00
Pack Size: 500g
Purity: 98%
in stock
$504.00 $353.00
Quantity
- +
Add to Card
Order Now
bulk Quotation Request
Technical Information
Catalog Number: AA0035KV
Chemical Name: Tetrabromothiophene
CAS Number: 3958-03-0
Molecular Formula: C4Br4S
Molecular Weight: 399.7238
MDL Number: MFCD00005419
SMILES: Brc1sc(c(c1Br)Br)Br
NSC Number: 65427
Properties
BP: 326°C at 760 mmHg  
Form: Solid  
MP: 116-118 °C(lit.);  
Storage: Keep in dry area;Room Temperature;  
Complexity: 96.7  
Covalently-Bonded Unit Count: 1  
Defined Atom Stereocenter Count: 0  
Defined Bond Stereocenter Count: 0  
Formal Charge: 0  
Heavy Atom Count: 9  
Hydrogen Bond Acceptor Count: 1  
Hydrogen Bond Donor Count: 0  
Isotope Atom Count: 0  
Rotatable Bond Count: 0  
Undefined Atom Stereocenter Count: 0  
Undefined Bond Stereocenter Count: 0  
XLogP3: 5  
Upstream Synthesis Route
3141-27-3    7664-41-7    1066-26-8    1003-09-4    3958-03-0 

[1]JournaloftheAmericanChemicalSociety,1953,vol.75,p.1764,1767

3141-27-3    7664-41-7    1003-09-4    3141-24-0    3958-03-0 

[1]JournaloftheAmericanChemicalSociety,1953,vol.75,p.1764,1767

188290-36-0    7726-95-6    1003-09-4    3141-27-3    3141-24-0    3958-03-0 

[1]ArkivfoerKemi,1957,vol.11,p.373,379,380

3958-03-0    3141-26-2 

[1]Patent:WO2004/58763,2004,A1,.Locationinpatent:Page41-42

3958-03-0    3141-26-2 

[1]JournalofOrganicChemistry,2008,vol.73,#1,p.323-326

[2]Synthesis,1990,#5,p.403-405

[3]Synthesis,1990,#5,p.403-405

[4]Chemistry-AEuropeanJournal,2004,vol.10,#13,p.3331-3340

[5]TetrahedronLetters,2004,vol.45,#17,p.3405-3407

[6]Patent:WO2004/58702,2004,A2,.Locationinpatent:Page32;24

[7]CanadianJournalofChemistry,1985,vol.63,p.2669-2672

[8]Patent:US2016/264595,2016,A1,.Locationinpatent:Paragraph0058;0060

[9]JournaloftheAmericanChemicalSociety,2007,vol.129,#26,p.8310-8319

[10]JournalofMaterialsChemistry,1999,vol.9,#8,p.1719-1725

[11]JournalofMaterialsChemistry,2012,vol.22,#1,p.100-108

[12]JournalofMolecularStructure,2000,vol.521,#1-3,p.285-301

[13]JournalofOrganicChemistry,1997,vol.62,#7,p.1940-1954

[14]ElectrochimicaActa,2010,vol.56,#1,p.326-332

[15]ActaChemicaScandinavica(1947-1973),1959,vol.13,p.1045

[16]ArkivfoerKemi,1957,vol.11,p.317,322

[17]JustusLiebigsAnnalenderChemie,1934,vol.512,p.136,156

[18]ChemistryofHeterocyclicCompounds(NewYork,NY,UnitedStates),1993,vol.29,#8,p.889-891

[19]KhimiyaGeterotsiklicheskikhSoedinenii,1993,#8,p.1046-1048

[20]ChemistryLetters,2003,vol.32,#8,p.744-745

[21]JournalofMaterialsChemistry,2012,vol.22,#11,p.4944-4952

[22]OrganicLetters,2012,vol.14,#19,p.5058-5061

[23]JournalofPolymerScience,PartA:PolymerChemistry,2017,vol.55,#16,p.2629-2638

Downstream Synthesis Route
188290-36-0    3958-03-0 

[1]TetrahedronLetters,2004,vol.45,p.3405-3407

[2]Chemistry-AEuropeanJournal,2004,vol.10,p.3331-3340

[3]JournalofMaterialsChemistryA,2020,vol.8,p.5315-5322

[4]JournaloftheAmericanChemicalSociety,2007,vol.129,p.8310-8319

[5]JournalofOrganicChemistry,2008,vol.73,p.323-326

[6]ElectrochimicaActa,2010,vol.56,p.326-332

[7]JournalofMaterialsChemistry,2012,vol.22,p.100-108

[8]Patent:US2016/264595,2016,A1.Locationinpatent:Paragraph0058;0059

[9]MolecularCrystalsandLiquidCrystals,2010,vol.524,p.17-25

[10]Patent:KR2015/39459,2015,A.Locationinpatent:Paragraph0197-0204

[11]JournalofMolecularStructure,2000,vol.521,p.285-301

[12]Tetrahedron,2017,vol.73,p.5847-5852

[13]Patent:KR101791161,2017,B1.Locationinpatent:Paragraph0204-0210

[14]Patent:WO2004/58702,2004,A2.Locationinpatent:Page31-32;24

[15]Patent:WO2004/58763,2004,A1.Locationinpatent:Page41-42

[16]BulletinoftheChemicalSocietyofJapan,1991,vol.64,p.2566-2568

[17]JournalofOrganicChemistry,1997,vol.62,p.1940-1954

[18]JournalofMaterialsChemistry,1999,vol.9,p.1719-1725

[19]JustusLiebigsAnnalenderChemie,1934,vol.512,p.136,156

[20]ChemischeBerichte,1883,vol.16,p.2172

[21]ChemistryLetters,2003,vol.32,p.744-745

[22]Molecules,2009,vol.14,p.1013-1031

[23]InorganicChemistry,2011,vol.50,p.10623-10632

[24]JournalofMaterialsChemistry,2012,vol.22,p.4944-4952

[25]AdvancedSynthesisandCatalysis,2012,vol.354,p.1819-1826

[26]ChemicalCommunications,2014,vol.50,p.15183-15186

[27]Macromolecules,2019,vol.52,p.6523-6532

3141-24-0    3958-03-0 

[1]ChemischeBerichte,1894,vol.27,p.2837

6933-26-2    3958-03-0 

[1]ChemischeBerichte,1893,vol.26,p.2458

31161-45-2    3958-03-0 

[1]ChemischeBerichte,1893,vol.26,p.2458

1003-09-4    3141-26-2    3141-24-0    3141-25-1    3958-03-0 

[1]SyntheticCommunications,1990,vol.20,p.2119-2122

Literature fold

Title: Efficient synthesis of thieno[3,2-b:4,5-b']diindoles and benzothieno[3,2-b]indoles by Pd-catalyzed site-selective C-C and C-N coupling reactions.

Journal: Organic & biomolecular chemistry20121207

Title: Selective mono- to perarylations of tetrabromothiophene by a cyclobutene-1,2-diylbisimidazolium preligand.

Journal: The Journal of organic chemistry20110916

Title: 2,3,4-Tribromo-thio-phene.

Journal: Acta crystallographica. Section E, Structure reports online20080401

Title: Structures of tetrabromothiophene and tetrabromoselenophene: the influence of the heteroatom on the heterophene packing.

Journal: Acta crystallographica. Section B, Structural science20071001

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