CAS 101328-85-2
:(5R)-6-(4-Aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone
Description:
(5R)-6-(4-Aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone, with the CAS number 101328-85-2, is a chemical compound characterized by its pyridazinone structure, which features a pyridazine ring fused with a carbonyl group and an amino group. This compound typically exhibits properties such as moderate solubility in polar solvents and potential biological activity due to the presence of the amino group, which can participate in hydrogen bonding and interact with biological targets. The stereochemistry indicated by the (5R) designation suggests a specific spatial arrangement of atoms, which can influence the compound's reactivity and interaction with other molecules. Its structural features may confer pharmacological properties, making it of interest in medicinal chemistry. Additionally, the presence of the methyl group and the phenyl ring can affect the compound's lipophilicity and overall stability. Overall, this compound's unique structure and functional groups contribute to its potential applications in various fields, including pharmaceuticals and agrochemicals.
Formula:C11H13N3O
InChI:InChI=1S/C11H13N3O/c1-7-6-10(15)13-14-11(7)8-2-4-9(12)5-3-8/h2-5,7H,6,12H2,1H3,(H,13,15)/t7-/m1/s1
InChI key:InChIKey=GDMRFHZLKNYRRO-SSDOTTSWSA-N
SMILES:C[C@H]1C(C2=CC=C(N)C=C2)=NNC(=O)C1
Synonyms:- (4R)-3-(4-Aminophenyl)-4-methyl-4,5-dihydro-1H-pyridazin-6-one
- (5R)-6-(4-Aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone
- (5R)-6-(4-Aminophenyl)-5-methyl-2,3,4,5-tetrahydropyridazin-3-one
- (5R)-6-(4-Aminophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-on
- (5R)-6-(4-Aminophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-one
- (R)-3(2H)Pyridazinone-6-(4-aminophenyl)-4,5-dihydro-5-methyl
- (R)-6-(4-Aminophenyl)-4,5-Dihydro-5-Methyl-3(2H)-Pyridazinone
- (R)-6-(4-Aminophenyl)-5-methyl-4,5-dihydropyridazin-3(2H)-one
- 3(2H)-Pyridazinone, 6-(4-aminophenyl)-4,5-dihydro-5-methyl-, (R)-
- 3(2H)-pyridazinone, 6-(4-aminophenyl)-4,5-dihydro-5-methyl-, (5R)-
- Or 1855
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Found 8 products.
3(2H)-Pyridazinone, 6-(4-aminophenyl)-4,5-dihydro-5-methyl-, (5R)-
CAS:Formula:C11H13N3OPurity:96%Color and Shape:SolidMolecular weight:203.2404Levosimendan Impurity 6
CAS:Formula:C11H13N3OColor and Shape:Pale Yellow Brown SolidMolecular weight:203.25OR-1855
CAS:OR-1855 is an active Levosimendan metabolite, has effect on human myometrial contractility.Formula:C11H13N3OPurity:98%Color and Shape:Pale Yellow SolidMolecular weight:203.24(R)-6-(4-Aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone
CAS:Controlled Product<p>Applications A metabolite of Levosimendan.<br>References Rubinstein, A., et al.: J. Pharmacol. Met., 19, 213 , (1988), Pollesello, P., et al.: J. Biol. Chem., 269, 28584 (1994), Yokoshiki, H., et al.: Eur. J. Pharmacol., 333, 249 (1997)<br></p>Formula:C11H13N3OColor and Shape:NeatMolecular weight:203.24(R)-6-(4-Aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone
CAS:<p>(R)-6-(4-Aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone is an alkalizing agent that is used to treat gout. It is also a calcium antagonist and can be used to treat familial mediterranean fever. (R)-6-(4-Aminophenyl)-4,5-dihydro-5-methyl-3(2H)-pyridazinone has been shown to inhibit the production of steroids and the function of meiosis in hamsters. The drug induces spontaneous meiotic arrest in animals and inhibits the formation of mature egg cells in female hamsters. It also acts as a reversible inhibitor of spindle formation in hamsters.</p>Formula:C11H13N3OPurity:Min. 95%Molecular weight:203.24 g/mol







