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18794-77-9,MFCD00022535
Catalog No.:AA002GHQ

18794-77-9 | 2-Hexylthiophene

Pack Size
Purity
Availability
Price(USD)
Quantity
  
1g
98%
in stock  
$6.00   $4.00
- +
5g
98%
in stock  
$14.00   $10.00
- +
10g
98%
in stock  
$26.00   $18.00
- +
25g
98%
in stock  
$52.00   $36.00
- +
  • 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:
AA002GHQ
Chemical Name:
2-Hexylthiophene
CAS Number:
18794-77-9
Molecular Formula:
C10H16S
Molecular Weight:
168.2990
MDL Number:
MFCD00022535
SMILES:
CCCCCCc1cccs1
FEMA Number:
4137
Properties
Properties
 
BP:
222°C at 760 mmHg  
Form:
Liquid  
MP:
-39.15°C (estimate)  
Refractive Index:
1.496  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
90.9  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
1  
Rotatable Bond Count:
5  
XLogP3:
4.4  

Upstream Synthesis Route

[1]OrganicLetters,2002,vol.4,#12,p.2067-2070

[2]JournalofOrganicChemistry,2009,vol.74,#7,p.2718-2725

[3]InorganicChemistry,2018,vol.57,#3,p.1527-1534

[4]ChineseChemicalLetters,2011,vol.22,#7,p.819-822

[5]BulletinoftheKoreanChemicalSociety,2012,vol.33,#11,p.3810-3816

[6]Tetrahedron,2013,vol.69,#38,p.8191-8198

[7]Tetrahedron,2007,vol.63,#25,p.5437-5449

[8]OrganicLetters,2013,vol.15,#6,p.1202-1205

[9]Macromolecules,2013,vol.46,#15,p.5985-5997

[10]DyesandPigments,2016,vol.124,p.222-231

[11]JournaloftheAmericanChemicalSociety,2006,vol.128,#7,p.2336-2345

[12]Patent:WO2010/670,2010,A1,.Locationinpatent:Page/Pagecolumn17-18

[13]Patent:WO2010/12710,2010,A1,.Locationinpatent:Page/Pagecolumn17

[14]JournaloftheAmericanChemicalSociety,2000,vol.122,#13,p.3037-3046

[15]Tetrahedron,2010,vol.66,#45,p.8778-8784

[16]InorganicChemistry,2016,vol.55,#13,p.6653-6659

[17]Chemistry-AnAsianJournal,2012,vol.7,#1,p.225-232

[18]JournaloftheAmericanChemicalSociety,2004,vol.126,#22,p.7015-7018

[19]Patent:US2012/247546,2012,A1,.Locationinpatent:Page/Pagecolumn37

[20]TetrahedronLetters,2007,vol.48,#5,p.779-784

[21]JournalofMaterialsChemistry,2007,vol.17,#14,p.1421-1426

[22]Patent:EP2138545,2009,A1,.Locationinpatent:Page/Pagecolumn17;33

[23]ChineseJournalofChemistry,2012,vol.30,#3,p.577-584

[24]JournalofPhysicalChemistryA,2012,vol.116,#30,p.7927-7936

[25]JournaloftheAmericanChemicalSociety,2012,vol.134,#42,p.17404-17407

[26]ScienceChinaChemistry,2013,vol.56,#7,p.997-1003

[27]DyesandPigments,2018,vol.157,p.179-189

[28]OrganicLetters,2018,

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,#32,p.10720-10728

[2]JournaloftheAmericanChemicalSociety,1951,vol.73,p.5240,5241

[3]JournaloftheAmericanChemicalSociety,1948,vol.70,p.391

[4]JournaloftheChemicalSociety,1955,p.1581,1583

[5]Errata,1957,

[1]Patent:US5118441,1992,A,

[2]Patent:US5395551,1995,A,

[1]Patent:US7692029,2010,B2,.Locationinpatent:Page/Pagecolumn17-18

[1]Macromolecules,2014,vol.47,#3,p.1008-1020

Downstream Synthesis Route

[1]JournaloftheAmericanChemicalSociety,2008,vol.130,p.10720-10728

[2]JournaloftheAmericanChemicalSociety,1951,vol.73,p.5240,5241

[3]JournaloftheAmericanChemicalSociety,1948,vol.70,p.391

[4]JournaloftheChemicalSociety,1955,p.1581,1583    Errata,1957

[1]JournaloftheAmericanChemicalSociety,1993,vol.115,p.8716-8721

[1]Heterocycles,2019,vol.99,p.1154-1169

[2]JournalofMaterialsChemistry,2008,vol.18,p.2234-2239

[3]JournaloftheAmericanChemicalSociety,1997,vol.119,p.10774-10784

[4]JournalofMaterialsChemistry,2005,vol.15,p.1446-1453

[5]DyesandPigments,2016,vol.124,p.222-231

[6]Tetrahedron,2007,vol.63,p.5437-5449

[7]JournaloftheAmericanChemicalSociety,2012,vol.134,p.17404-17407

[8]TetrahedronLetters,2003,vol.44,p.5879-5882

[9]Patent:EP1985669,2008,A1.Locationinpatent:Page/Pagecolumn11

[10]AngewandteChemie-InternationalEdition,2011,vol.50,p.2799-2803

[11]DyesandPigments,2011,vol.91,p.404-412

[12]Patent:JP5816111,2015,B2.Locationinpatent:Paragraph0176;0180

[13]Patent:JP2015/86268,2015,A.Locationinpatent:Paragraph0095-0097

[1]OrganicLetters,2011,vol.13,p.5208-5211

[2]OrganicLetters,2014,vol.16,p.2330-2333

[3]Patent:EP2138545,2009,A1.Locationinpatent:Page/Pagecolumn17-18;33

[4]JournalofMaterialsChemistryC,2013,vol.1,p.3467-3481

[5]Chemistry-AnAsianJournal,2012,vol.7,p.225-232

[6]DyesandPigments,2015,vol.113,p.458-464

[7]JournaloftheAmericanChemicalSociety,2006,vol.128,p.2336-2345

[8]BulletinoftheKoreanChemicalSociety,2012,vol.33,p.3810-3816

[9]Tetrahedron,2013,vol.69,p.8191-8198

[10]Macromolecules,2014,vol.47,p.1008-1020

[11]JournalofOrganicChemistry,1998,vol.63,p.5497-5506

[12]OrganicLetters,2013,vol.15,p.1202-1205

[13]OrganicLetters,2002,vol.4,p.2067-2070

[14]OrganicLetters,2004,vol.6,p.273-276

[15]JournaloftheAmericanChemicalSociety,2005,vol.127,p.2406-2407

[16]TetrahedronLetters,2007,vol.48,p.779-784

[17]OrganicLetters,2018,vol.20,p.7270-7273

[18]Tetrahedron,2010,vol.66,p.8778-8784

[19]JournalofMaterialsChemistry,2002,vol.12,p.2706-2721

[20]MolecularCrystalsandLiquidCrystals,2004,vol.410,p.1/

[529]-12/

[540]

[21]MolecularCrystalsandLiquidCrystalsScienceandTechnology,SectionA:MolecularCrystalsandLiquidCrystals,2001,vol.364,p.881-888

[22]AngewandteChemie-InternationalEdition,2011,vol.50,p.10682-10685

[23]ChineseJournalofChemistry,2012,vol.30,p.577-584

[24]JournalofPhysicalChemistryA,2012,vol.116,p.7927-7936

[25]ScienceChinaChemistry,2013,vol.56,p.997-1003

[26]Chemistry-AnAsianJournal,2016,vol.11,p.2932-2937

[27]CrystEngComm,2018,vol.20,p.1669-1678

[28]DyesandPigments,2018,vol.157,p.179-189

18794-77-9   
5,5’-bishexyl-2,2’-bithiophene 

[1]OrganicLetters,2014,vol.16,p.2732-2735

[2]JournalofMaterialsChemistryC,2014,vol.2,p.8152-8161

[3]JournaloftheAmericanChemicalSociety,2011,vol.133,p.2402-2405

[4]JournalofOrganicChemistry,1998,vol.63,p.5497-5506

[5]AngewandteChemie-InternationalEdition,2013,vol.52,p.3117-3120    Angew.Chem.,2013,vol.125,p.3199-3202,4

Literature

Title: Nanoscale structure, dynamics and power conversion efficiency correlations in small molecule and oligomer-based photovoltaic devices.

Journal: Nano reviews 20110101

Title: Efficient synthesis of carbazolyl- and thienyl-substituted beta-diketonates and properties of their red- and green-light-emitting Ir(III) complexes.

Journal: The Journal of organic chemistry 20090403

Title: 2,6-Diarylnaphtho[1,8-bc:5,4-b'c']dithiophenes as new high-performance semiconductors for organic field-effect transistors.

Journal: Journal of the American Chemical Society 20050316

Title: Ozawa H, et al. Ruthenium sensitizers with a hexylthiophene-modified terpyridine ligand for dye-sensitized solar cells: synthesis, photo- and electrochemical properties, and adsorption behavior to the TiO2 surface.ACS Appl Mater Interfaces. 2015 Feb 11;7(5):3152-61.

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