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Merck
CN

402176

6,8-Dibromo-3-formylchromone

99%

Synonym(s):

6,8-Dibromo-4-oxo-4H-1-benzopyran-3-carboxaldehyde

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About This Item

Empirical Formula (Hill Notation):
C10H4Br2O3
CAS Number:
42059-76-7
Molecular Weight:
331.94
NACRES:
NA.22
PubChem Substance ID:
24865057
UNSPSC Code:
12352100
MDL number:
MFCD00191991
Assay:
99%
Form:
solid

Key Documents

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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.

pictograms

Skull and crossbones
GHS06

signalword

Danger

hcodes

H301

Hazard Classifications

Acute Tox. 3 Oral

Storage Class

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

Regulatory Information

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Certificates of Analysis (COA)

Lot/Batch Number
MKBN4357V
13718JR
07015MF
09126HO

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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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