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Merck
CN

C3103

咔唑

96%

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关于此项目

经验公式(希尔记法):
C12H9N
化学文摘社编号:
分子量:
167.21
EC Number:
201-696-0
UNSPSC Code:
12352103
PubChem Substance ID:
Beilstein/REAXYS Number:
3956
MDL number:
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vapor pressure

400 mmHg ( 323 °C)

assay

96%

form

powder

bp

355 °C (lit.)

mp

243-246 °C (lit.)

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



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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
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
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