7343-59-1 Usage
Chemical class
Dinitrobenzene derivatives
Structure
Benzene ring with two nitro groups (-NO2) and a hexylsulfanyl group (-S-(CH2)5CH3) attached
Functional groups
Nitro groups, Sulfonyl group
Applications
a. Organic synthesis
b. Precursor or intermediate in chemical production
c. Development of pharmaceuticals
d. Development of agrochemicals
Toxicity
Toxic, should be handled with caution
Physical state
Likely a solid (based on similar compounds)
Solubility
Likely soluble in organic solvents (e.g., ethanol, acetone) due to the presence of a nonpolar hexyl chain
Stability
May be sensitive to heat, light, or moisture due to the presence of nitro groups
Reactivity
Reactive towards nucleophiles and reducing agents due to the presence of nitro groups
Hazards
Potential health hazards (respiratory, skin, eye irritation) and environmental hazards (aquatic toxicity, soil contamination) due to its toxicity and chemical structure
Check Digit Verification of cas no
The CAS Registry Mumber 7343-59-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,4 and 3 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 7343-59:
(6*7)+(5*3)+(4*4)+(3*3)+(2*5)+(1*9)=101
101 % 10 = 1
So 7343-59-1 is a valid CAS Registry Number.
7343-59-1Relevant articles and documents
Short Wavelength Inner Filter Technique (SWIFT) in Designing Reactive Fluorescent Molecular Probes
Baheti, Abhishek,Vigalok, Arkadi
, p. 12224 - 12228 (2019/08/21)
Here, we present a conceptually novel and experimentally straightforward technique for selective analyte detection that uses a combination of commercial fluorophores and simple chemicals. The technique utilizes the well-known inner filter effect (IFE); however, the fluorophore's excitation is performed at wavelengths significantly shorter than its absorption maximum. In the presence of the analyte, the "filter" appears or disappears at the excitation wavelength resulting in the fluorescence turning OFF or ON, respectively. Unlike common probes, our technique allows real-time monitoring of a fluorophore's stability as well as its recycling. We further demonstrate the applicability of this technique in continuing analyte detection as well as vapor analysis.