Abstract: In an electrophotographic light-sensitive material having on a conductive support a light-sensitive layer composed of a charge generating material and a charge transporting material. A hydrazone compound is used as the charge transporting material for providing the light sensitive layer having high sensitivity and less residual surface potential. The light-sensitive layer is stable to oxidation by ozone generated by corona discharging as well as to heat and light, results in less dark decay of the surface potential. Furthermore, the layer shows less deviation in residual potential and sensitivity due to repeated use.

Abstract: An electrophotographic photosensitive member is characterized by having a layer containing at least one of hydrazone group compounds represented by the following formula (1) or of ketazine group compounds represented by the following formula (2): ##STR1## In the formula, R.sub.11 and R.sub.12 independently of one another represent hydrogen, substituted or unsubstituted aryl, or substituted or unsubstituted heterocyclic radical; R.sub.13 and R.sub.14 independently of one another represent subsituted or unsubstituted alkyl, substituted or unsubstituted aralkyl, substituted or unsubstituted aryl, or substituted or unsubstituted heterocyclic radical; and R.sub.15 represents a divalent organic residue. ##STR2## In the formula, R.sub.21, R.sub.22, R.sub.23, and R.sub.24 independently one another represent substituted or unsubstituted alkyl, substituted or substituted aralkyl, or substituted or unsubstituted aryl, or R.sub.21 and R.sub.

Abstract: Electrophotographic light-sensitive elements containing substituted or unsubstituted fluorenone hydrazones as charge generating or charge transport materials are described.

Abstract: An electrophotographic photosensitive member having a layer containing at least one compound represented by the formula ##STR1## wherein X.sub.1 represents a residue necessary for completing a substituted or unsubstituted aromatic hydrocarbon ring; X.sub.2 represents a residue necessary for completing a substituted or unsubstituted heterocyclic ring; R.sub.1, R.sub.2, R.sub.3, and A each represent hydrogen, alkyl, aralkyl, or aryl, substituted or unsubstituted; and m is 0 or 1.

Abstract: An electrophotographic element which comprises a conductive substrate and a photosensitive layer, superposed thereon, consisting of a charge generation layer and a charge transport layer, said charge transport layer containing as an available ingredient a hydrazone compound having the following general formula (I): ##STR1## (where R is a hydrogen atom, an alkyl group, of from one to six carbon atoms, an alkoxyl group of from one to six carbon atoms, a substituted or non-substituted dialkylamino group, halogen, a nitro group or a hydroxyl group. n is an integer of 1-5. In case where n is 2 or more, R may be the same or different.).

Abstract: Hydrazone derivatives of the formula ##STR1## in which A.sub.1 is an aromatic radical, B.sub.1 is hydrogen, alkyl, cycloalkyl, aralkyl or aryl, R.sub.1, R.sub.2 and R.sub.3 independently of one another are alkyl, cycloalkyl, aralkyl or polyoxyalkylene, Z.sub.1 is arylene, X.sup..crclbar. is an anion and m is 0, 1, 2 or 3.The hydrazone derivatives are suitable as UV absorbers, especially in polymer coatings.

Abstract: Novel substituted 11-amino-undeca-4,8-dienal and 11-amino-undecanal aldehyde-derivatives of the formulae Ia ##STR1## in which R.sub.1 to R.sub.6, Y and m are as defined in patent claim 1, and processes for their preparation are described. The compounds of the formulae Ia and Ib can be catalytically hydrogenated to novel 1,11-diaminoundecanes, which, in turn, can be used, for example, for the preparation of polycondensation products, in particular transparent polyamides, or as curing agents for epoxide resins.

Abstract: Novel compounds are described which are substituted benzophenone hydrazones. They have pesticidal activity, especially against insects and acarids, and pesticidal compositions and methods are described. Methods of making the compounds, and novel intermediates, are also described.

Abstract: 4,5-Diaryl-.alpha.-(polyfluoroalkyl)-1H-pyrrole-2-methanamines such as 4,5-bis(4-fluorophenyl)-.alpha..alpha.-bis-(trifluoromethyl)-1H-pyrrole-2- methanamine, useful in treatment of inflammation.

Abstract: The invention relates to a process for the production of 1-(4-chlorobenzoyl)-5-methoxy-2-methyl-3-indolylacetoxyacetic acid (known to be useful as an antiphlogistic agent) which comprises reacting .alpha.-(4-chlorobenzoyl)-4-methoxyphenylhydrazine hydrochloride or sulphonate with laevulinoyloxyacetic acid and cyclizing the resulting hydrazone to obtain a product free from 1-benzoyl-5-methoxy-2-methyl-3-indolylacetoxyacetic acid.

Abstract: Hydrazone compounds having the general formula ##STR1## wherein Ar is selected from the group consisting of a naphthalene ring radical, substituted naphthalene ring radicals, an anthracene ring radical, substituted anthracene ring radicals, styryl, substituted styryls, a pyridine radical, a furan ring radical and a thiophene ring radical.The hydrazone compounds can be prepared by allowing 1-methyl-1-phenylhydrazine having the formula ##STR2## to react with an aldehyde represented by the general formula Ar-CHO, wherein Ar is the same as mentioned above at a substantially equal molar ratio in an organic solvent selected from the group consisting of lower alcohols, cyclic ethers, cellosolves, N,N-dimethylforamide and acetic acid, in the presence of an acid catalyst, by heating and refluxing the reaction mixture.

Abstract: Novel compounds are described which are substituted benzophenone hydrazones. They have pesticidal activity, especially against insects and acarids, and pesticidal compositions and methods are described. Methods of making the compounds, and novel intermediates, are also described.

Abstract: Novel substituted 11-amino-undeca-4,8-dienal and 11-amino-undecanal aldehyde-derivatives of the formulae Ia ##STR1## in which R.sub.1 to R.sub.6, Y and m are as defined in patent claim 1, and processes for their preparation are described. The compounds of the formulae Ia and Ib can be catalytically hydrogenated to novel 1,11-diaminoundecanes, which, in turn, can be used, for example, for the preparation of polycondensation products, in particular transparent polyamides, or as curing agents for epoxide resins.

Abstract: Novel 4-monoalkylamino-benzaldehydes, 4-mono-alkylamino-alkanophenones, and 4-monoalkylamino-benzophenones, and derivatives and salts thereof, are disclosed which are useful as anti-atherosclerotic agents.

Abstract: This disclosure describes anthracene-9,10-bis-carbonyl-hydrazones and derivatives thereof useful as antibacterial agents, for inhibiting the growth of transplanted mouse tumors, and for inducing the regression and/or palliation of leukemia and related cancers.

Abstract: This invention relates to copolymerizable ultraviolet light absorber compounds having the formula: ##STR1## where R is alkylene, C.sub.1 -C.sub.10, hydroxyalkylene, C.sub.1 -C.sub.10, alkylene-oxyalkylene, C.sub.1 -C.sub.10 or phenylene, C.sub.1 -C.sub.10, unsubstituted or substituted with hydroxy;R' and R" are independently hydrogen or akyl; C.sub.1 -C.sub.6 ; and R"' is hydrogen or akyl, C.sub.1 -C.sub.6.

Abstract: This disclosure describes 9,10-dihydroanthracene-9,10-dicarboxaldehyde-bis-hydrazones and derivatives thereof useful as antibacterial agents, for inhibiting the growth of transplanted mouse tumors, and for inducing the regression and/or palliation of leukemia and related cancers in mammals.