6-bromo-3-formylchromone
Names
[ CAS No. ]:
52817-12-6
[ Name ]:
6-bromo-3-formylchromone
[Synonym ]:
6-BroMo-3-forMylchroMone
MFCD00191849
6-bromo-4-oxochromene-3-carbaldehyde
6-Bromo-4-oxo-4H-1-benzopyran-3-carboxaldehyde
6-Bromochromone-3-carboxaldehyde
Chemical & Physical Properties
[ Density]:
1.835g/cm3
[ Boiling Point ]:
365.7ºC at 760 mmHg
[ Melting Point ]:
190-193 °C(lit.)
[ Molecular Formula ]:
C10H5BrO3
[ Molecular Weight ]:
253.04900
[ Flash Point ]:
175ºC
[ Exact Mass ]:
251.94200
[ PSA ]:
47.28000
[ LogP ]:
2.36800
[ Index of Refraction ]:
1.713
MSDS
Safety Information
[ Symbol ]:
GHS07
[ Signal Word ]:
Warning
[ Hazard Statements ]:
H315-H319-H335
[ Precautionary Statements ]:
P261-P305 + P351 + P338
[ Personal Protective Equipment ]:
dust mask type N95 (US);Eyeshields;Gloves
[ Hazard Codes ]:
Xi
[ Risk Phrases ]:
R36/37/38
[ Safety Phrases ]:
S26-S36
[ RIDADR ]:
NONH for all modes of transport
[ WGK Germany ]:
3
[ HS Code ]:
2914700090
Customs
[ HS Code ]: 2914700090
[ Summary ]:
HS: 2914700090 halogenated, sulphonated, nitrated or nitrosated derivatives of ketones and quinones, whether or not with other oxygen function Tax rebate rate:9.0% Supervision conditions:none VAT:17.0% MFN tariff:5.5% General tariff:30.0%
Articles
Bioorg. Med. Chem. 19 , 3367-71, (2011)
Series of chromone containing sulfonamides were prepared by the reaction of (un)substituted 3-formylchromones with 3-aminobenzenesulfonamide and 4-aminobenzenesulfonamide. Bovine carbonic anhydrase (b...
Multidrug resistance reversal by 3-formylchromones in human colon cancer and human mdr1 gene-transfected mouse lymphoma cells.In Vivo 20(5) , 645-9, (2006)
Several new 3-formylchromone derivatives proved to be modifiers of multidrug resistance in mouse lymphoma cells and in human Colo320 colon cancer cells. There is apparently a structure-activity relati...
Biological activity of 3-formylchromones and related compounds.In Vivo 21(5) , 829-34, (2007)
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...