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About This Item
Empirical Formula (Hill Notation):
C10H8S
CAS Number:
Molecular Weight:
160.24
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Assay
95%
bp
256 °C (lit.)
mp
34-36 °C (lit.)
functional group
phenyl
storage temp.
2-8°C
SMILES string
c1ccc(cc1)-c2cccs2
InChI
1S/C10H8S/c1-2-5-9(6-3-1)10-7-4-8-11-10/h1-8H
InChI key
PJRGDKFLFAYRBV-UHFFFAOYSA-N
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
228.2 °F - closed cup
Flash Point(C)
109 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Some Substitution Reactions of 2-Phenylthiophene.
Gjos N and Gronowit S.
Acta Chemica Scandinavica, 26, 1851-1859 (1972)
Microwave-assisted synthesis of 2-acetyl-5-arylthiophenes and 4-(5-arylthiophen-2-yl) thiazoles via Suzuki coupling in water.
Dawood KM, et al.
ARKIVOC (Gainesville, FL, United States), 7, 50-62 (2015)
On the nitration of 2-and 3-phenylthiophene.
Gronowitz SALO and Gios N.
Acta Chemica Scandinavica, 21(10), 16-16 (1967)
Ji He et al.
Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology, 16(7), 1049-1056 (2017-05-13)
Three D-D-π-A triphenylamine-coumarin sensitizers were designed and synthesized with a triphenylamine and coumarin double donor and a cyanoacrylic acid acceptor. Thiophene, bithiophene and phenylthiophene were used as π-bridges, respectively, and the effects of different π-bridges on the photophysical properties and
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