Chemical Properties and Facts of 7661-33-8

Although many compounds look similar to this compound(7661-33-8)Application of 7661-33-8, numerous studies have shown that this compound(SMILES:O=C1N(C2=CC=C(Cl)C=C2)CCC1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Application of 7661-33-8. The reaction of aromatic heterocyclic molecules with protons is called protonation. Aromatic heterocycles are more basic than benzene due to the participation of heteroatoms. Compound: 1-(4-Chlorophenyl)pyrrolidin-2-one, is researched, Molecular C10H10ClNO, CAS is 7661-33-8, about Condensation of aniline, o-phenylenediamine, and their derivatives with lactones. Author is Shazhenov, A. A.; Kadyrov, Ch. Sh.; Kurbanov, P..

Heating equimol. amounts of RNH2 and γ-butyrolactone at 130-305° gave 2-pyrrolidinones (I) (R and % yield given): Ph, 80; m-MeC6H4, 75; p-MeC6H4, 78; m-BrC6H4, 60; α-naphthyl, 14; m-CF3C6H4, 19; p-ClC6H4, 77; β-naphthyl, 62. Boiling a mixture of equimol. amounts of substituted aromatic o-diamines and γ- or β-lactones in xylene gave the following 3-(2-benzimidazolyl)-1-alkanoles (II) (R1, R2, X, and % yield given): H, CCl3, CH2, 61; Cl, CCl3, CH2, 85; Me, CCl3, CH2, 87; H, H, (CH2)2, 80; Cl, H, (CH2)2, 24; Me, H, (CH2)2, 31; H, Me, (CH2)2, 78; H, Pr, (CH2)2, 78; Cl, Pr, (CH2)2, 7; Me, Pr, (CH2)2, 13; H, Bu, (CH2)2, 75; Cl, Bu, (CH2)2, 17; H, C7H15, (CH2)2, 66; H, H, CHOHCMe2, 50; H, H, CHAcCH2, 40; Cl, H, CHAcCH2, 16. Uv data for II are given.

Although many compounds look similar to this compound(7661-33-8)Application of 7661-33-8, numerous studies have shown that this compound(SMILES:O=C1N(C2=CC=C(Cl)C=C2)CCC1), has unique advantages. If you want to know more about similar compounds, you can read my other articles.

Reference:
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