17173-83-0 Usage
Appearance
Yellow crystalline powder The compound has a yellow color and a crystalline structure in its solid form.
Melting point
139-141°C The compound transitions from a solid to a liquid state within this temperature range.
Solubility
Sparingly soluble in water 2,6-Distyryl-4H-pyran-4-one does not dissolve easily in water.
Photochromic properties
Ability to change color when exposed to light The compound can alter its color in response to light exposure, making it useful in various applications.
Organic optoelectronic devices
Potential applications in these devices 2,6-Distyryl-4H-pyran-4-one has been studied for its possible use in devices that convert light into electrical energy or vice versa.
Fluorescent probe
Used for detecting metal ions The compound can be utilized as a probe to identify and measure the presence of metal ions.
Antioxidant properties
Capable of neutralizing free radicals 2,6-Distyryl-4H-pyran-4-one has been investigated for its potential to counteract oxidative stress and damage.
Antibacterial properties
Potential to inhibit bacterial growth The compound shows promise in fighting against bacterial infections and preventing their spread.
Check Digit Verification of cas no
The CAS Registry Mumber 17173-83-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,1,7 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 17173-83:
(7*1)+(6*7)+(5*1)+(4*7)+(3*3)+(2*8)+(1*3)=110
110 % 10 = 0
So 17173-83-0 is a valid CAS Registry Number.
17173-83-0Relevant articles and documents
Synthesis and spectroscopic properties of cross-conjugated ketones and meso-substituted tridecamethine salts containing the pyran or pyridone fragment
Krasnaya,Smirnova,Shvedova,Tatikolov,Kuz'min
, p. 2029 - 2037 (2003)
The reactions of substituted 4H-pyrones and N-methyl-2,6-dimethylpyridone with dimethylformamide acetal and aminal acetals of conjugated ω-dimethylaminoaldehydes were studied. Cross-conjugated ketones and meso-ethoxy(dialkylamino)tridecamethine salts cont