Decrypt The Mystery Of 87488-84-4

This compound(1-(2-Bromophenyl)-1H-pyrazole)Recommanded Product: 1-(2-Bromophenyl)-1H-pyrazole was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

The chemical properties of alicyclic heterocycles are similar to those of the corresponding chain compounds. Compound: 1-(2-Bromophenyl)-1H-pyrazole, is researched, Molecular C9H7BrN2, CAS is 87488-84-4, about Catalytic, Directed C-C Bond Functionalization of Styrenes, the main research direction is alkene dealkenylative alkenylation rhodium catalyst; allyl alc dealkenylation rhodium catalyst.Recommanded Product: 1-(2-Bromophenyl)-1H-pyrazole.

A method for catalytic conversion of C(aryl)-C(alkenyl) bonds in styrene derivatives R1-2-R2C6H3C(=CHR4)R3 (R1 = H, 4-Me, 3-Cl, 5-Me, etc.; R2 = 1-pyrazolyl, 2-pyridyl; R3 = H, Me, Ph, 4-methoxyphenyl, etc.; R4 = H, Ph, 4-chlorophenyl) to new C-C bonds is developed. In the presence of a rhodium catalyst, the alkenyl groups of styrenes bearing a pyrazolyl directing group were efficiently converted to other carbon substituents upon reacting with various alkenes RCH=CH2 (R = 4-methylhex-1-en-1-yl, 2-cyclohexylethenyl, 2-phenylethenyl, etc.) and allyl alcs. R5CH(OH)CH=CH2(R5 = cyclohexyl, Me, Et, etc.). It is also indicated that the C-C bond cleavage proceeded via a hydrometalation/β-carbon elimination pathway.

This compound(1-(2-Bromophenyl)-1H-pyrazole)Recommanded Product: 1-(2-Bromophenyl)-1H-pyrazole was discussed at the molecular level, the effects of temperature and reaction time on the properties of the compound were discussed, and the optimum reaction conditions were selected.

Reference:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem