<Suppliers Price>

alpha-Terthiophene

Names

[ CAS No. ]:
1081-34-1

[ Name ]:
alpha-Terthiophene

[Synonym ]:
Terthiophene
2,2':5',2"-Terthiophene
2,2':5',2''-Terthiophene
2,2':5'2''-Terthiophene
2,2:5,2-Terthiophene
a-Terthienyl
MFCD00012167
5-(2-Thienyl)-2,2'-bithiophene
2,5-Di(2-thienyl)thiophene
α-Terthienyl
2,5-dithiophen-2-ylthiophene
[2,2';5',2'']Terthiophene

Biological Activity

[Description]:

2,2':5',2''-Terthiophene (α-Terthiophene) is an oligomer of the heterocycle thiophene. 2,2':5',2''-Terthiophene has been employed as building block for the organic semi-conductor polythiophene.

[Related Catalog]:

Signaling Pathways >> Others >> Others

[In Vitro]

In the most common isomer of Terthiophene, two thienyl groups are connected via their 2 positions to a central thiophene, also at the carbon atoms flanking the sulfur.

[References]

[1]. Casado J, et al. Alternated quinoid/aromatic units in terthiophenes building blocks for electroactive narrow band gap polymers. Extended spectroscopic, solid state, electrochemical, and theoretical study. J Phys Chem B. 2005 Sep 8;109(35):16616-27.


[Related Small Molecules]

Captisol | Cyclosporin A | H2DCFDA | 0MPTP hydrochloride | GW4869 | Etomoxir | TD139 | Mitoquinone mesylate | GSK2795039 | JC-1 | BAPTA-AM | AP 20187 | Setanaxib (GKT137831) | D-Luciferin | Crotaline

Chemical & Physical Properties

[ Density]:
1.3±0.1 g/cm3

[ Boiling Point ]:
361.3±32.0 °C at 760 mmHg

[ Melting Point ]:
93-95 °C(lit.)

[ Molecular Formula ]:
C12H8S3

[ Molecular Weight ]:
248.387

[ Flash Point ]:
128.4±11.3 °C

[ Exact Mass ]:
247.978806

[ PSA ]:
84.72000

[ LogP ]:
5.56

[ Vapour Pressure ]:
0.0±0.8 mmHg at 25°C

[ Index of Refraction ]:
1.672

[ Storage condition ]:
2-8°C

MSDS

Toxicological Information

CHEMICAL IDENTIFICATION

RTECS NUMBER :
WZ9717750
CAS REGISTRY NUMBER :
1081-34-1
LAST UPDATED :
199606
DATA ITEMS CITED :
1
MOLECULAR FORMULA :
C12-H8-S3
MOLECULAR WEIGHT :
248.38

HEALTH HAZARD DATA

ACUTE TOXICITY DATA

TYPE OF TEST :
LD50 - Lethal dose, 50 percent kill
ROUTE OF EXPOSURE :
Intraperitoneal
SPECIES OBSERVED :
Rodent - rat
DOSE/DURATION :
110 mg/kg
TOXIC EFFECTS :
Details of toxic effects not reported other than lethal dose value
REFERENCE :
PHTOEH Pharmacology and Toxicology (Copenhagen). (Munksgaard International Pub., POB 2148, DK-1016 Copenhagen K, Denmark) V.60- 1987- Volume(issue)/page/year: 77,164,1995

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ Hazard Codes ]:
F: Flammable;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S22-S24/25

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

[ RTECS ]:
WZ9717750

[ HS Code ]:
2934999090

Synthetic Route

Customs

[ HS Code ]: 2934999090

[ Summary ]:
2934999090. other heterocyclic compounds. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

Length-dependent conductance of oligothiophenes.

J. Am. Chem. Soc. 136(29) , 10486-92, (2014)

We have measured the single-molecule conductance of a family of oligothiophenes comprising 1-6 thiophene moieties terminated with methyl-sulfide linkers using the scanning tunneling microscope-based b...

Radical-scavenging activity of melatonin, either alone or in combination with vitamin E, ascorbate or 2-mercaptoethanol as co-antioxidants, using the induction period method.

In Vivo 25(1) , 49-53, (2011)

Melatonin shows antioxidant/prooxidant activity but its mechanism of action remains unknown.The radical-scavenging activity of melatonin and various melatonin/co-antioxidant mixtures in a 1:1 molar ra...

Synthesis and evaluation of new spacers for use as dsDNA end-caps.

Bioconjug. Chem. 21(8) , 1545-53, (2010)

A series of aliphatic and aromatic spacer molecules designed to cap the ends of DNA duplexes have been synthesized. The spacers were converted into dimethoxytrityl-protected phosphoramidites as syntho...


More Articles


Related Compounds

The content on this webpage is sourced from various professional data sources. If you have any questions or concerns regarding the content, please feel free to contact service1@chemsrc.com.