1,3,5-tri(thiophen-2-yl)benzene

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Company Name: J & K SCIENTIFIC LTD.  
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Company Name: Meryer (Shanghai) Chemical Technology Co., Ltd.  
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1,3,5-tri(thiophen-2-yl)benzene manufacturers

1,3,5-tri(thiophen-2-yl)benzene Basic information
Product Name:1,3,5-tri(thiophen-2-yl)benzene
Synonyms:1,3,5-tri(thiophen-2-yl)benzene;1,3,5-Tri(2-thienyl)benzene;1,3,5-Tris(2-thienyl)benzene;Thiophene, 2,2',2''-(1,3,5-benzenetriyl)tris-;2,2',2''-(1,3,5-Benzenetriyl)tris[thiophene;2-[3,5-bis(2-thienyl)phenyl]thiophene;1,3,5-Tri(thiophen-2-yl)benzene - [T94289]
CAS:15509-95-2
MF:C18H12S3
MW:324.48
EINECS:695-506-7
Product Categories:
Mol File:15509-95-2.mol
1,3,5-tri(thiophen-2-yl)benzene Structure
1,3,5-tri(thiophen-2-yl)benzene Chemical Properties
Melting point 157.0 to 161.0 °C
Boiling point 298°C/10mmHg(lit.)
density 1.278±0.06 g/cm3(Predicted)
storage temp. Storage temp. 2-8°C
solubility soluble in Toluene
form powder to crystal
color White to Light yellow
InChI1S/C18H12S3/c1-4-16(19-7-1)13-10-14(17-5-2-8-20-17)12-15(11-13)18-6-3-9-21-18/h1-12H
InChIKeyUBHPRZXDFVCNHZ-UHFFFAOYSA-N
SMILESc1csc(c1)-c2cc(cc(c2)-c3cccs3)-c4cccs4
Safety Information
Hazard Codes T
Risk Statements 25
Safety Statements 45
RIDADR UN 2811 6.1 / PGIII
WGK Germany 3
HS Code 2934.99.4400
Storage Class6.1D - Non-combustible acute toxic Cat.3
toxic hazardous materials or hazardous materials causing chronic effects
Hazard ClassificationsAcute Tox. 3 Oral
MSDS Information
1,3,5-tri(thiophen-2-yl)benzene Usage And Synthesis
Uses1,3,5-Tris(2-thienyl)benzene is a trifunctionalized monomer that can be used in the synthesis of conjugated C3-symmetric poly(arylbenzene) polymers. These polymeric materials can further be used in organic photovoltaic devices as well as organic field effect transistors (OFETs) and organic light emitting diodes (OLED) systems.
General Description1,3,5-Tris(2-thienyl)benzene is a 1,3,5 tris substituted benzene that has a three dimensional structure which facilitates the preparation of conjugating polymers. It is a branched conductive monomer with electronically attached nodes that provide a suitable support to increase the conductivity of the synthesized polymers.
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