CAS 7659-29-2
:3,5-Dinitrocatechol
Description:
3,5-Dinitrocatechol is an organic compound characterized by the presence of two nitro groups (-NO2) and a catechol structure, which consists of a benzene ring with two hydroxyl groups (-OH) positioned at the 1 and 2 positions. This compound is typically a yellow crystalline solid and is known for its potential applications in various fields, including pharmaceuticals and as a reagent in chemical synthesis. The presence of nitro groups contributes to its reactivity, making it a useful intermediate in the synthesis of other chemical compounds. 3,5-Dinitrocatechol is also notable for its ability to participate in redox reactions due to the electron-withdrawing nature of the nitro groups, which can influence its chemical behavior and stability. Additionally, it may exhibit biological activity, although specific effects can vary based on concentration and environmental conditions. As with many nitro compounds, safety precautions should be taken when handling 3,5-Dinitrocatechol due to its potential toxicity and environmental impact.
Formula:C6H4N2O6
InChI:InChI=1S/C6H4N2O6/c9-5-2-3(7(11)12)1-4(6(5)10)8(13)14/h1-2,9-10H
InChI key:InChIKey=VDCDWNDTNSWDFJ-UHFFFAOYSA-N
SMILES:N(=O)(=O)C1=CC(N(=O)=O)=CC(O)=C1O
Synonyms:- 3,5-Dinitro-1,2-benzenediol
- 3,5-Dinitrocatechol
- 1,2-Benzenediol, 3,5-dinitro-
- Pyrocatechol, 3,5-dinitro-
- 3,5-Dinitropyrocatechol
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Found 10 products.
OR-486
CAS:Controlled Product<p>Applications OR 486 is an anti-inflammatory agent used in the treatment of rheumatoid arthritis and osteoarthritis. Entacapone (E588500) impurity.<br>References Jenei-Lanzl, Z. et al.: Annal Rheum. Dis., 74, 444 (2015); Karlsson, M., et al.: J. Pharm. Biomed. Anal., 10, 593 (1992), Nissinen, E., et al.: Arch. Pharmacol., 346, 262 (1992), Wikberg, T., et al.: Eur. J. Drug Metab. Pharmacokinet., 18, 359 (1993),<br></p>Formula:C6H4N2O6Color and Shape:NeatMolecular weight:200.11OR-486
CAS:<p>OR-486 is a basic dye with pharmacological properties. It has been shown to have low-energy fluorescence, and it can be used for the detection of dopamine. OR-486 can also inhibit catechol-o-methyltransferase (COMT), an enzyme that catalyzes the methylation of catecholamines, including dopamine and epinephrine. In addition, OR-486 inhibits xanthine oxidase (XO) in vitro and in vivo. It has been shown to be effective against diabetic neuropathy in Sprague-Dawley rats as well as deficient mice. OR-486 has also been shown to increase the uptake of glucose by cells in a plate test.</p>Formula:C6H4N2O6Purity:Min. 95%Molecular weight:200.11 g/mol3,5-Dinitrocatechol
CAS:<p>OR-486 is an inhibitor of catechol-O-methyl-transferase(COMT) and can be used to prepare the molybdenum (VI)- 3,5-Dinitrocatechol complex.</p>Formula:C6H4N2O6Purity:99.8%Color and Shape:SolidMolecular weight:200.11









