alpha-Terthiophene

Modify Date: 2025-08-22 18:05:15

alpha-Terthiophene Structure
alpha-Terthiophene structure
Common Name alpha-Terthiophene
CAS Number 1081-34-1 Molecular Weight 248.387
Density 1.3±0.1 g/cm3 Boiling Point 361.3±32.0 °C at 760 mmHg
Molecular Formula C12H8S3 Melting Point 93-95 °C(lit.)
MSDS Chinese USA Flash Point 128.4±11.3 °C

 Use of alpha-Terthiophene


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.

 Names

Name 2,2':5',2''-terthiophene
Synonym More Synonyms

 alpha-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
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.

 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
InChIKey KXSFECAJUBPPFE-UHFFFAOYSA-N
SMILES c1csc(-c2ccc(-c3cccs3)s2)c1
Storage condition 2-8°C

 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%

 Articles35

More 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...

 Synonyms

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
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