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Merck
CN

C3103

Carbazole

96%

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About This Item

Empirical Formula (Hill Notation):
C12H9N
CAS Number:
Molecular Weight:
167.21
EC Number:
201-696-0
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
3956
MDL number:
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InChI key

UJOBWOGCFQCDNV-UHFFFAOYSA-N

InChI

1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H

SMILES string

c1ccc2c(c1)[nH]c3ccccc23

vapor pressure

400 mmHg ( 323 °C)

assay

96%

form

powder

bp

355 °C (lit.)

mp

243-246 °C (lit.)

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Guodong Ji et al.
Journal of hazardous materials, 225-226, 1-7 (2012-05-23)
We examined the effects of power and treatment time on the ultrasonically enhanced ozonation of carbazole dissolved in APG(1214) surfactant solutions, including an analysis of the mechanism of OH radical formation, the zeta potential of the colloidal suspension, the influence
Cheng He et al.
Chemical communications (Cambridge, England), 49(6), 627-629 (2012-12-12)
A photoactive basket-like metal-organic tetragon Ce-ZL that contained a carbazole photosensitizer was developed to capture the biomimetic [FeFe]-H(2)ases for light driven H(2) production. The system exhibited enzymatic behaviour and its activity was inhibited by the encapsulation of ATP.
Jae-Min Suk et al.
Organic letters, 14(19), 5018-5021 (2012-09-18)
Chiral organic anions such as camphorsulfonates and cAMP give rise to the preferential formation of a one-handed helix of an indolocarbazole foldamer, thus inducing characteristic circular dichroic (CD) signals. Moreover, the on and off switching of the chiroptical signal can
Xiaofeng Liu et al.
Advanced materials (Deerfield Beach, Fla.), 24(33), 4505-4510 (2012-06-22)
An arylated-carbazole conjugated polymer with a deep HOMO level has been developed. Solar cells based on blends of PCX3 and PC(71) BM show efficiency of 3.9% with a V(oc) of 0.96 V. The device performance can be improved to 5.1%
Shen H Tan et al.
Organic letters, 14(22), 5621-5623 (2012-10-31)
The racemic modification of the Aspidosperma alkaloid limaspermidine (1) has been prepared in ten steps including one involving a Raney-cobalt-mediated tandem reductive cyclization of nitrile 8 to give the tetracyclic system 9b. Compound (±)-1 has been converted over two steps

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