46100
Carbazole
VETRANAL®, analytical standard
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Fórmula empírica (notación de Hill):
C12H9N
Número CAS:
Peso molecular:
167.21
UNSPSC Code:
41116107
NACRES:
NA.24
PubChem Substance ID:
EC Number:
201-696-0
Beilstein/REAXYS Number:
3956
MDL number:
Servicio técnico
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analytical standard
Quality Level
vapor pressure
400 mmHg ( 323 °C)
product line
VETRANAL®
shelf life
limited shelf life, expiry date on the label
technique(s)
HPLC: suitable, gas chromatography (GC): suitable
bp
355 °C (lit.)
mp
243-246 °C (lit.)
application(s)
clinical
environmental
format
neat
SMILES string
c1ccc2c(c1)[nH]c3ccccc23
InChI
1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H
InChI key
UJOBWOGCFQCDNV-UHFFFAOYSA-N
Legal Information
VETRANAL is a registered trademark of Merck KGaA, Darmstadt, Germany
signalword
Warning
hcodes
Hazard Classifications
Aquatic Chronic 4 - Carc. 2 - Muta. 2
Clase de almacenamiento
11 - Combustible Solids
wgk
WGK 2
flash_point_f
428.0 °F - closed cup
flash_point_c
220.0 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
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Jong-Kwan Bin et al.
Advanced materials (Deerfield Beach, Fla.), 24(21), 2911-2915 (2012-05-03)
A new carbazole derivative with two carbazole moieties on the C3 and C6 positions of carbazole and triphenylsilane directly linked to the N of carbazole is successfully used as a highly efficient blue phosphorescent host in an organic light-emitting diode
Shin-ichiro Kato et al.
The Journal of organic chemistry, 77(20), 9120-9133 (2012-09-19)
A large series of conjugated carbazole dimers, namely bicarbazoles 1-12, were synthesized by Suzuki-Miyaura, Sonogashira, Hay, and McMurry coupling reactions. In 1-12, the two carbazole moieties are linked at the 1-, 2-, or 3-position directly or via an acetylenic or
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