The asymmetric C atom in the title compound, C(21)H(17)BrClNO, is in a slightly distorted tetra-hedral environment and the NH unit adopts a gauche orientation with respect to the CO group. In the crystal, pairs of inter-molecular N-H⋯O hydrogen bonds form centrosymmetric dimers.

The [4.3.0]heterobicyclic title structure, C(19)H(14)BNO(3), is composed of a five-membered OBNC(2) ring and a six-membered OBNC(3) ring, each of which has an approximate envelope conformation. The coordination geometry of the B atom is distorted tetra-hedral. In the crystal structure, centrosymmetrically related mol-ecules are associated through pairs of O-H⋯O hydrogen bonds.

The mol-ecule of the title compound, [Sn(C(5)H(5)S)(4)], lies on a special position of site symmetry. The Sn(IV) atom shows a slightly distorted tetra-hedral coordination.

The aim of research the synthesis 5,11,17,23-tetra(t-butyl)-25-monohydroxy-26,27,28-tribenzoyloxycalix[4]arene (TBMTCA) material were by one-step synthesized benzoylation reaction 5,11,17,23-tetra(t-butyl)-25,26,27,28-tetrahydroxycalix[4]arene (TBCA) and benzoyl chloride is (1: 3,7) mol refluxing 3 hours at room temperature predicted mechanism models. product was carried out means FTIR 1H-NMR s...

Synthesized of novel metal (II)- tetra-4-(N,N-dimethyl phenyl) methan-imine phthalocyanines (MTDMPhImPc) [ M = Co, Ni, Cu, Zn] by an effective and suitable method. The tetra-nitrophthalocyanines converted into aminophthalocyanines reduction. Than amino derivatives bearing to form tetra substituted 4-(N,N-dimethyl methane-imine complexes. These compounds were characterized FTIR, elemental analys...