Skip to Content
Merck
CN
All Photos(1)

Key Documents

View All Documentation

Safety Information

402176

Sigma-Aldrich

6,8-Dibromo-3-formylchromone

99%

Synonym(s):

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

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

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

Assay

99%

form

solid

mp

174-176 °C (lit.)

functional group

aldehyde
bromo
ketone

SMILES string

[H]C(=O)C1=COc2c(Br)cc(Br)cc2C1=O

InChI

1S/C10H4Br2O3/c11-6-1-7-9(14)5(3-13)4-15-10(7)8(12)2-6/h1-4H

InChI key

XTEURQCXJDIUCR-UHFFFAOYSA-N

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

Signal Word

Danger

Hazard Statements

H301

Precautionary Statements

P301 + P310

Hazard Classifications

Acute Tox. 3 Oral

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

新产品

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKBN4357V
13718JR
07015MF
09126HO

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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.

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