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2,2':5',2''-TERTHIOPHENE

2,2':5',2''-TERTHIOPHENE Structure
CAS No.
1081-34-1
Chemical Name:
2,2':5',2''-TERTHIOPHENE
Synonyms
3TH;TTh;S1130;2,2':5';2,2':5',2;terthienyl;TERTHIOPHENE;a-Terthienyl;5-BroMo-[2,2';JACS-1081-34-1
CBNumber:
CB7713541
Molecular Formula:
C12H8S3
Molecular Weight:
248.39
MOL File:
1081-34-1.mol
MSDS File:
SDS
Modify Date:
2024/11/19 23:02:33

2,2':5',2''-TERTHIOPHENE Properties

Melting point 93-95 °C(lit.)
Boiling point 160 °C (0.1 mmHg)
Density 1.4602 (rough estimate)
refractive index 1.6200 (estimate)
Flash point 160°C/0.1mm
storage temp. Keep in dark place,Sealed in dry,Room Temperature
solubility Chloroform (Slightly), Methanol (Slightly)
form Solid
color Light Yellow
Water Solubility Insoluble in water.
Merck 14,9174
BRN 178604
CAS DataBase Reference 1081-34-1(CAS DataBase Reference)
EPA Substance Registry System .alpha.-Terthiophene (1081-34-1)

SAFETY

Risk and Safety Statements

Symbol(GHS) 
GHS07
Signal word  Warning
Hazard statements  H315-H319-H335
Precautionary statements  P261-P305+P351+P338
Risk Statements  36/37/38
Safety Statements  22-24/25
WGK Germany  3
RTECS  WZ9717750
8-10
HS Code  29349990
NFPA 704
0
1 0

2,2':5',2''-TERTHIOPHENE price More Price(3)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Sigma-Aldrich(India) 311073 2,2′:5′,2′′-Terthiophene 99% 1081-34-1 1G ₹9910 2022-06-14 Buy
TCI Chemicals (India) T1196 2,2':5',2''-Terthiophene (purified by sublimation) min. 99.0 % 1081-34-1 1G ₹5300 2022-05-26 Buy
TCI Chemicals (India) T1196 2,2':5',2''-Terthiophene (purified by sublimation) min. 99.0 % 1081-34-1 5G ₹10800 2022-05-26 Buy
Product number Packaging Price Buy
311073 1G ₹9910 Buy
T1196 1G ₹5300 Buy
T1196 5G ₹10800 Buy

2,2':5',2''-TERTHIOPHENE Chemical Properties,Uses,Production

Chemical Properties

YELLOW TO YELLOW-BROWN POWDER

Uses

α-Terthienyl was first recognized as a nematicidal constituent of marigolds, but in the presence of light, it is also highly toxic to larvae of several insect species, including mosquitoes. This electron donor thiophenederivative phototoxin is biosynthesized from polyacetylene precursors and appears to function as a photosensitizer catalyzing the formation of reactive oxygen species at the target site (25).

General Description

2,2′:5′,2′′-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard′s reagent derived from 2-bromothiophene and magnesium. It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes. It also exihibits antifungal activity.

Metabolic pathway

When 14C-a-terthienyl is administered orally to rats in a single dose, two metabolites [1,4-di(2'-thienyl)]-1,4- butadione and 2-2' -bithiophene-5-carboxylic acid are identified in the urine.

Purification Methods

Possible impurities are bithienyl and polythienyls. Suspend it in H2O and steam distil it to remove bithienyl. The residue is cooled and extracted with CHCl3, dried (MgSO4), filtered, evaporated and the residue chromatographed on Al2O3 using pet ether/3% Me2CO as eluent. The terphenyl zone is then eluted from the Al2O3 with Et2O, the extract is evaporated and the residue is recrystallised from MeOH (40mL per g). The platelets are washed with cold MeOH and dried in air. [UV: Sease & Zechmeister J Am Chem Soc 69 270 1947; Uhlenbroek & Bijloo Recl Trav Chim Pays-Bas 79 1181 1960.] It has also been recrystallised from MeOH, *C6H6, pet ether or AcOH. [UV: Zechmeister & Sease J Am Chem Soc 69 273 1947, Steinkopf et al. Justus Liebigs Ann Chem 546 180 1941.] It is a phototoxic nematocide [Cooper & Nitsche Bioorg Chem 13 36 1985, Chan et al. Phytochem 14 2295 1975]. [Beilstein 19 III/IV 4763, 19/9 V 226.]

2,2':5',2''-TERTHIOPHENE Preparation Products And Raw materials

Global( 324)Suppliers
Supplier Tel Country ProdList Advantage Inquiry
Sapala Organics Private Limited +91-4027170174 +91-9963110948 Telangana, India 89 58 Inquiry
Rivashaa Agrotech Biopharma Pvt. Ltd. +91-26463395 +91-7926462688 Gujarat, India 1615 58 Inquiry
Denisco Chemicals Pvt Ltd +91-9989050751 Telangana, India 249 58 Inquiry
TCI Chemicals (India) Pvt. Ltd. 1800 425 7889 New Delhi, India 6768 58 Inquiry
Gagri Global IT Services Pvt. Ltd. +91-40-27170174, Telangana, India 1321 58 Inquiry
CHEMSWORTH +91-261-2397244 New Delhi, India 6700 30 Inquiry
A.J Chemicals 91-9810153283 New Delhi, India 6100 58 Inquiry
Hebei Mojin Biotechnology Co., Ltd +86 13288715578 +8613288715578 China 12840 58 Inquiry
Shanghai UCHEM Inc. +862156762820 +86-13564624040 China 7514 58 Inquiry
Henan Fengda Chemical Co., Ltd +86-371-86557731 +86-13613820652 China 20287 58 Inquiry
2,5-BIS(2-THIENYL)THIOPHENE 2,5-DI(2-THIENYL)THIOPHENE 2,2′:5′,2′′-Terthiophene,α-Terthienyl, 2,5-Di(2-thienyl)thiophene 2,2':5',2-TERTHIENYL 2,2',5',2''-TERTHIOPHENE 2,2':5',2''-Terthiophene 99% 2,2':5',2''-Terthiophene (purified by sublimation) ALPHA-TERTHIENYL 2,5-Di(thien-2-yl)thiophene 2,2 :5 ,2 -Terthiophene  2,5-Di(2-thienyl)thiophene alpha-Terthienyl 2,2':5',2''-Terthiophene (=α-Terthienyl) 5-BroMo-[2,2' 2,2':5',2''-TERTHIOPHENE TERTHIOPHENE alpha-terthiophene terthienyl alpha-TERTHIENYL (2,2':5',2 5',2''Terthiophene 2,2':5' 2''-TERTHIOPHENE 2,2':5',2''-Terthiophene (=alpha-Terthienyl) α-Terthienyl, 2,5-Di(2-thienyl)thiophene Alpha-terthienyl,99+% 2,5-Bis(thiophene-2-yl)thiophene a-Terthienyl 2,2':5',2''-Terthiophene ,99% 2,3-dithiophen-2-ylthiophene 3TH 2,5-Di(2-thienyl)thiophene alpha-Terth TTh Alpha-trithiophene JACS-1081-34-1 2,2':5',2''-Terthiophene, 99%, for synthesis α-Terthiophene 2,2':5',2''-TERTHIOPHENE ISO 9001:2015 REACH S1130 Sanlian thiophene 2,2':5',2''-Terthiophene (7CI, 8CI, 9CI, ACI) Osa(2-octen-1-ylsuccinic anhydride, mixture of cis and trans) 2,2 ': 5', 2 '' - Trithiophene 2,2',2''-Terthiophene 2,2':5',2''-Terthiophene 2,2',2''-Terthiophene 2,2':5',2"-Terthiophene 2,2':5',2 2,2':5',2'-TERTHIOPHENE 2,2,5,2-Terthiophene in isooctane 2,2,5,2-Terthiophene in toluene 1081-34-1 1081-34-4 108-34-1 C12H8S3 Heterocyclic Building Blocks Thiophenes Building Blocks Reagents for Conducting Polymer Research Thiophene Derivatives (for Conduting Polymer Research)