Sexithiophene

Base Information

Chemical Name:Sexithiophene
CAS No.:88493-55-4
Molecular Formula:C24H14 S6
Molecular Weight:494.771
Hs Code.:29349990
European Community (EC) Number:626-183-2
DSSTox Substance ID:DTXSID90462870
Nikkaji Number:J602.557I
Wikidata:Q72507451
Mol file:88493-55-4.mol

Synonyms:sexithiophene

Suppliers and Price of Sexithiophene

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Sexithiophene
100mg
$ 70.00

TCI Chemical
α-Sexithiophene (purified by sublimation)
100mg
$ 26.00

TCI Chemical
α-Sexithiophene (purified by sublimation)
1g
$ 144.00

Sigma-Aldrich
α-Sexithiophene
1g
$ 132.00

American Custom Chemicals Corporation
ALPHA-SEXITHIOPHENE 95.00%
1G
$ 851.41

American Custom Chemicals Corporation
ALPHA-SEXITHIOPHENE 95.00%
100MG
$ 590.67

AK Scientific
alpha-Sexithiophene
100mg
$ 82.00

Total 32 raw suppliers

Chemical Property of Sexithiophene

Chemical Property:

Appearance/Colour:solid
Vapor Pressure:4.23E-14mmHg at 25°C
Melting Point:290 ºC (dec.)(lit.)
Boiling Point:608.5°C at 760 mmHg
Flash Point:245.5°C
PSA：169.44000
Density:1.402
LogP:10.39060
XLogP3:8.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:5
Exact Mass:493.94197749
Heavy Atom Count:30
Complexity:536

Purity/Quality:

≥99% ^*data from raw suppliers

Sexithiophene ^*data from reagent suppliers

Safty Information:

Pictogram(s): Xi
Hazard Codes:Xi
Statements: 36
Safety Statements: 26-36

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CSC(=C1)C2=CC=C(S2)C3=CC=C(S3)C4=CC=C(S4)C5=CC=C(S5)C6=CC=CS6
Uses Sexithiophene is an organic semiconductor/transistor.

Technology Process of Sexithiophene

There total 12 articles about Sexithiophene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 84.0%

: 94581-95-0
5-bromo-2,2':5',2''-terthiophene

: 88493-55-4
sexithiophene

Guidance literature:: With potassium fluoride; bis(pinacol)diborane; (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; In methanol; toluene; at 70 ℃; for 0.166667h; microwave irradiation;
DOI:10.1021/jo035723q

Reference yield: 81.0%

: 492-97-7
2,2'-Bithiophene

: 5632-29-1
quaterthiophene

: 113728-71-5
2,2':5',2'':5'',2''':5''',2'''':5'''',2''''':5''''',2'''''':5'''''',2'''''''-octithiophene

: 88493-55-4
sexithiophene

Guidance literature:: 2,2'-Bithiophene; With mercury(II) trifluoroacetate; In benzene; at 0 ℃; for 0.25h;

With triethylamine; palladium dichloride; In benzene; at 0 ℃; for 0.25h; Further stages.;
DOI:10.1021/jo025838e

Reference yield: 70.0%

: 188290-36-0,8014-23-1,25233-34-5
thiophene

: 5632-29-1
quaterthiophene

: 113728-71-5
2,2':5',2'':5'',2''':5''',2'''':5'''',2''''':5''''',2'''''':5'''''',2'''''''-octithiophene

: 88493-55-4
sexithiophene

Guidance literature:: thiophene; With mercury(II) trifluoroacetate; In benzene; at 0 ℃; for 0.25h;

With triethylamine; palladium dichloride; In benzene; at 0 ℃; for 0.25h; Further stages.;
DOI:10.1021/jo025838e