Abstract: A larger service area can be ensured, and a trouble such as a reduction in service area or the interruption of communication which is caused when an obstructive exists on a manhole cover is quickly prevented. A wall portion that defines a space in which a transmit/receive antenna is disposed has such a slope as to expand the space from a base station unit toward an upper surface portion of the manhole cover, and an angle of slope varies depending on the dimensions of the service area. Also, when the existence of the obstructive on the manhole cover is detected by use of a pressure sensor or an electric wave sensor, the control of the communication operation of a mobile station is switched to another base station without calculating or processing an electric field intensity in the base station.

Abstract: A supporting member for an electron gun, which is molded and processed from a composition comprising a glass component and an additive, wherein the additive is a material which does not decompose in a temperature range for the molding and processing and which decomposes and evaporates for the first time in the temperature range for embedding an electrode metal in the surface of the supporting member.

Abstract: A herbicidal composition comprising a herbicidally effective amount of N-halogenoacylanilino-fatty acid or the ester derivative thereof represented by the general formula: ##STR1## wherein R.sub.1 and R.sub.2 each represents C.sub.1 -C.sub.4 allyl, R.sub.3 represents a hydrogen atom, alkyl having up to 10 carbon atoms, C.sub.3 -C.sub.5 alkenyl, C.sub.3 -C.sub.4 alkynyl or cyclohexyl, R.sub.4 represents lower alkyl substituted by 1-4 halogen atoms and Y represents C.sub.1 -C.sub.3 alkylene, as an effective ingredient, and a herbicidally effective inert carrier.

Abstract: 1-Cycloalkylcarbonyl-3-(3,5-dihalophenyl)imidazolidine-2,4-diones of the formula: ##STR1## wherein X is a chlorine or bromine atom, R.sub.1 is a C.sub.3 -C.sub.6 cycloalkyl, tetramethylcyclopropyl, 2,2-dimethyl-3-isobutenylcyclopropyl or 2,2-dimethyl-3-dichlorovinylcyclopropyl group and R.sub.2 and R.sub.3 are individually a hydrogen atom or a methyl group, which show high fungicidal activities without any material toxicity to mammals and plants and which can be produced by reacting the corresponding 1-unsubstituted compound with a cycloalkanecarboxylic acid or a reactive derivative thereof.

Abstract: N-(3,5-Dihalophenyl)-.alpha.-spirocycloalkanesuccinimides of the formula: ##STR1## wherein X is a chlorine or bromine atom and R is a C.sub.3 -C.sub.6 alkylene group, which show high fungicidal activities without any material toxicity to mammals and plants and which can be produced by reacting the corresponding .alpha.-spirocycloalkanesuccinic acid or its anhydride with 3,5-dichloroaniline or 3,5-dibromoaniline.

Abstract: 3-(3',5'-Dihalophenyl)-1-sulfenylimidazolidine-2,4-diones of the formula: ##STR1## wherein X is a chlorine atom or a bromine atom, Y.sub.1, Y.sub.2 and Y.sub.3 are each a chlorine atom or a fluorine atom and R.sub.1 and R.sub.2 are individually a hydrogen atom or a methyl group, which show high microbicidal activities against various fungi without any material toxicity to mammals and plants and can be produced by reacting the corresponding 1-unsubstituted compound with a sulfenyl halide.

Abstract: Novel N-(3,5-dihalophenyl)cyclopropanedicarboximides of the formula: ##STR1## wherein X and Y are each a chlorine atom or a bromine atom and R.sub.1, R.sub.2 and R.sub.3 are individually a hydrogen atom or a methyl group, which show high microbicidal activities against various fungi and bacteria without any material toxicity to mammals and plants and which can be produced by reacting the corresponding cyclopropanedicarboxylic acid or its anhydride with a 3,5-dihaloaniline.

Abstract: 3-(3' -Dihalophenyl)-1-sulfonylimidazolidine-2,4-5'-diones of the formula: ##STR1## wherein X is a halogen atom, R.sub.1 is a C.sub.1 -C.sub.12 alkyl group, a C.sub.2 -C.sub.4 alkenyl group or a halogenated C.sub.1 -C.sub.4 alkyl group having 1 to 3 halogen atoms, and R.sub.2 and R.sub.3 are individually a hydrogen atom or a methyl group, which show high microbicidal activities against various fungi and bacteria without any material toxicity to mammals and which plants and can be produced by reacting the corresponding 1-unsubstituted compound with a sulfonyl halide.

Abstract: Novel N-substituted amino acid derivatives of the formula: ##STR1## wherein R.sub.1 is an alkenyl group having 2 to 5 carbon atoms, a halogen-substituted alkenyl group having 2 to 5 carbon atoms or an alkynyl group having 2 to 5 carbon atoms, R.sub.2 is a methyl or ##STR2## group in which R.sub.2 ' is an alkyl group having 1 to 4 carbon atoms or a halogen-substituted alkyl group having 1 to 4 carbon atoms; and R.sub.3 is a hydrogen atom, an alkyl having 1 to 20 carbon atoms, cycloalkyl having 3 to 6 carbon atoms, benzyl, hydroxyethyl or methoxyethyl group, and inorganic or organic acid addition salts thereof, which possess useful soil fungicidal activities and can be produced by reacting a sarcosine derivative of the formula:CH.sub.3 HNCH.sub.2 COOR.sub.3 (II)wherein R.sub.3 is as defined above, with a halogen compound of the formula:R.sub.1 -- X (III)wherein R.sub.1 is as defined above and X is a halogen atom, or by reacting an N-substituted glycine derivative of the formula: ##STR3## wherein R.sub.1 and R.

Abstract: N-substituted-aminoacetamide compounds having the formula (I) ##STR1## wherein R.sub.1 represents a lower alkenyl group having up to 5 carbon atoms, a halogen-substituted lower alkenyl group having up to 5 carbon atoms or a lower alkynyl group having up to 5 carbon atoms, R.sub.2 and R.sub.3, which may be the same or different, each represents a hydrogen atom or a lower akyl group having up to 4 carbon atoms, and the inorganic and organic acid addition salts thereof, which are useful as fungicidal agents, processesfor preparing N-substituted-aminoacetamide compounds and fungicidal compositions containing at least one compound of the formula (I) as an active inredient.

Abstract: Novel N-(3,5-dihalophenyl)imide compounds, which exhibit a strong antimicrobial activity against microorganisms including phytopathogenic fungi, parasites of industrial products and pathogenic microorganisms, represented by the formula, ##STR1## wherein X and X' each represent halogens and A represents a substituted ethylene such as chloroethylene, C.sub.1 - C.sub.4 alkylthioethylene, C.sub.1 - C.sub.2 alkyl-ethylene or 1,2-di-C.sub.1 - C.sub.2 -alkyl-ethylene, a cyclopropylene such as 1,3-dimethylcyclopropylene, trimethylene, a cyclohexylene-1,2-, cyclohexenylene-1,2-, cyclohexadienylene-1,2- or o-phenylene.The N-(3,5-dihalophenyl)imide compounds can be obtained by any of methods which produce imide compounds or reaction of an N-(3,5-dihalophenyl)maleimide compound with a mercaptan, a hydrogen halide, phosphorus chloride or thionylchloride.

Abstract: N-substituted aminonitrile derivatives of the formula (I) ##EQU1## wherein R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are as hereinafter defined, useful as fungicides, method for their preparation, and fungicidal compositions containing the N-substituted aminonitrile derivatives of the formula (I).