C3103
Carbazole
96%
Sign In to View Organizational & Contract Pricing.
Select a Size
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:
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.)
Looking for similar products? Visit Product Comparison Guide
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service