262684
9-Phenylcarbazole
≥99%, purified by sublimation
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About This Item
Empirical Formula (Hill Notation):
C18H13N
CAS Number:
Molecular Weight:
243.30
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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Assay
≥99%
form
solid
purified by
sublimation
mp
95-97 °C (lit.)
SMILES string
c1ccc(cc1)-n2c3ccccc3c4ccccc24
InChI
1S/C18H13N/c1-2-8-14(9-3-1)19-17-12-6-4-10-15(17)16-11-5-7-13-18(16)19/h1-13H
InChI key
VIJYEGDOKCKUOL-UHFFFAOYSA-N
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General description
The electrochemical coupling and dimerization behavior of 9-phenylcarbazole has been investigated.
Application
9-Phenylcarbazole has been used in the electrochemical synthesis of poly(9-phenylcarbazole) films via direct anodic oxidation in mixed electrolytes of boron trifluoride diethyl etherate and sulfuric acid.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Aquatic Chronic 4 - Eye Dam. 1 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Olena Yurchenko et al.
The journal of physical chemistry. B, 116(1), 30-39 (2011-12-14)
The electrochemical coupling and dimerization behavior of the low molecular compounds triphenylamine (TPA) and 9-phenylcarbazole (PHC) in comparison to tri-p-tolylamine (p-TTA) with para-blocked methyl groups has been investigated in detail. In contrast to the unsubstituted radical cations of TPA and
Electrochemical polymerization of 9-phenylcarbazole in mixed electrolytes of boron trifluoride diethyl etherate and sulfuric acid.
Zeng L, et al.
J. Mater. Sci., 43(3), 1135-1143 (2008)
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