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经验公式(希尔记法):
C10H4Br2O3
化学文摘社编号:
分子量:
331.94
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Form:
solid
InChI
1S/C10H4Br2O3/c11-6-1-7-9(14)5(3-13)4-15-10(7)8(12)2-6/h1-4H
SMILES string
[H]C(=O)C1=COc2c(Br)cc(Br)cc2C1=O
InChI key
XTEURQCXJDIUCR-UHFFFAOYSA-N
assay
99%
form
solid
mp
174-176 °C (lit.)
functional group
aldehyde, bromo, ketone
Gene Information
human ... PTPN1(5770)
General description
6,8-Dibromo-3-formylchromone is a 3-formylchromone derivative. It is reported to exhibit inhibitory activity against the urease.
Application
6,8-Dibromo-3-formylchromone may be used in the preparation of (E)-N′-((6,8-dibromo-4-oxo-4H-chromen-3-yl)methylene)-1-naphthohydrazide.
signalword
Danger
hcodes
pcodes
Hazard Classifications
Acute Tox. 3 Oral
存储类别
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges
法规信息
新产品
此项目有
Yoshinobu Ishikawa et al.
Acta crystallographica. Section E, Structure reports online, 70(Pt 12), 522-524 (2015-01-02)
The title compound, C21H12Cl2N2O3, is a 1,4-diaroyl pyrazole derivative and has three aromatic rings. The dihedral angles between the naphthalene ring system and the pyrazole ring, the pyrazole and phenyl rings and the naphthalene ring system and the phenyl ring
Masami Kawase et al.
In vivo (Athens, Greece), 21(5), 829-834 (2007-11-21)
Several 3-formylchromone derivatives were examined for their tumor cell-cytotoxic, anti-Helicobacter pylori, urease inhibitory and anti-HIV activity. Comparing their relative cytotoxicity against four human tumor cell lines and three normal human cells, tumor cell-specific cytotoxicity was detected in some 3-formylchromone derivatives.
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