CAS 125628-97-9
:(3,4-Dihydroxy-5-nitrophenyl)(2-fluorophenyl)methanone
Description:
(3,4-Dihydroxy-5-nitrophenyl)(2-fluorophenyl)methanone, with the CAS number 125628-97-9, is a chemical compound characterized by its complex structure, which includes a phenyl ring substituted with hydroxyl and nitro groups, as well as a fluorinated phenyl moiety. This compound typically exhibits properties associated with both phenolic and nitro functionalities, which can influence its reactivity and solubility. The presence of hydroxyl groups suggests potential for hydrogen bonding, while the nitro group may impart electron-withdrawing characteristics, affecting the compound's overall electronic properties. The fluorine atom can enhance lipophilicity and alter the compound's interaction with biological systems. Such structural features often contribute to the compound's potential applications in pharmaceuticals, agrochemicals, or as intermediates in organic synthesis. Additionally, the compound's stability, melting point, and solubility in various solvents would be important characteristics to consider for practical applications. Overall, this compound represents a unique combination of functional groups that can lead to diverse chemical behavior.
Formula:C13H8FNO5
InChI:InChI=1S/C13H8FNO5/c14-9-4-2-1-3-8(9)12(17)7-5-10(15(19)20)13(18)11(16)6-7/h1-6,16,18H
InChI key:InChIKey=RQPAUNZYTYHKHA-UHFFFAOYSA-N
SMILES:C(=O)(C1=CC(N(=O)=O)=C(O)C(O)=C1)C2=C(F)C=CC=C2
Synonyms:- Methanone, (3,4-Dihydroxy-5-Nitrophenyl)(2-Fluorophenyl)-
- Or 1139
- Ro 41-0960
- (3,4-Dihydroxy-5-nitrophenyl)(2-fluorophenyl)methanone
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Found 4 products.
(3,4-Dihydroxy-5-nitrophenyl)(2-fluorophenyl)methanone
CAS:<p>(3,4-Dihydroxy-5-nitrophenyl)(2-fluorophenyl)methanone</p>Purity:99%Molecular weight:277.21g/mol(3,4-Dihydroxy-5-nitrophenyl)(2-fluorophenyl)methanone
CAS:<p>3,4-Dihydroxy-5-nitrophenyl)(2-fluorophenyl)methanone (NSC 663128) is a potent and selective growth factor that binds to the dopamine receptor. It has been shown to inhibit protein tyrosine phosphorylation and cell proliferation in vitro. This compound has also been shown to protect against neurotoxicity induced by methamphetamine in rats. NSC 663128 has also demonstrated an anti-cancer effect on human cancer cells, including leukemia cells and breast cancer cells. The mechanism of this effect may be due to inhibition of catechol-o-methyltransferase, epidermal growth factor receptor, or other cellular targets.</p>Formula:C13H8FNO5Purity:Min. 95%Molecular weight:277.2 g/molRo 41-0960
CAS:<p>Ro 41-0960 is used as a reversible and orally-active COMT-inhibitor.</p>Formula:C13H8FNO5Purity:98%Color and Shape:SolidMolecular weight:277.2




