Isoquinoline can crystallizes in platelets that have a low solubility in water but dissolve well in ethanol, acetone, diethyl ether, carbon disulfide, and other common organic solvents. 1532-97-4, formula is C9H6BrN, Name is 4-Bromoisoquinoline. It is also soluble in dilute acids as the protonated derivative. Recommanded Product: 4-Bromoisoquinoline.
Cardenas, Jorge;Gavino, Ruben;Garcia-Rios, Erendira;Rios-Ruiz, Lucero;Puello-Cruz, Ana C.;Morales-Serna, Francisco Neptali;Gomez, Samuel;Lopez-Torres, Adolfo;Morales-Serna, Jose Antonio research published 《 The Heck reaction of allylic alcohols catalysed by an N-heterocyclic carbene-Pd(II) complex and toxicity of the ligand precursor for the marine benthic copepod Amphiascoides atopus》, the research content is summarized as follows. The palladium-catalyzed reaction of aryl halides and allylic alcs. was an attractive method for obtaining α,β-unsaturated aldehydes and ketones, which represent key intermediates in organic synthesis. In this context, a 1,2,3-triazol-5-ylidene (aNHC)-based palladium(II) complex formed in situ was found to be a selective catalyst for the syntheses of building blocks from the corresponding aryl halides and allylic alcs., with yields ranging from 50% to 90%. The lack of toxic effects of the ligand precursor (1,2,3-triazolium salt) of the palladium(II) complex for the harpacticoid copepod Amphiascoides atopus allowed to contrast the efficiency of the catalytic system with the potential impact of the principal waste chem. in global aquatic ecosystems, which has not been previously addressed.
Recommanded Product: 4-Bromoisoquinoline, 4-Bromoisoquinoline, also known as 4-Bromoisoquinoline, is a useful research compound. Its molecular formula is C9H6BrN and its molecular weight is 208.05 g/mol. The purity is usually 95%.
4-Bromoisoquinoline is an aryl halide that can be used in the cross-coupling reaction with other aryl halides. It has been shown to have anticancer activity and to inhibit the growth of tumour cell lines in vitro. This compound is also efficient for inhibiting leukemia cells. 4-Bromoisoquinoline has been shown to have an inhibitory effect on cancer cells through the inhibition of DNA synthesis and RNA transcription, as well as by inducing apoptosis. The mechanism of action may be due to its ability to bind to aromatic hydrocarbons and halides, which leads to thermodynamic changes and vibrational energy transfer., 1532-97-4.
Referemce:
Isoquinoline – Wikipedia,
Isoquinoline | C9H7N – PubChem