Abstract: Carbon dioxide electrolysis apparatus includes: electrolysis stack having diaphragm including anion exchange type solid polymer electrolyte membrane and anode and cathode separated by diaphragm; carbon dioxide supply unit configured to supply carbon dioxide to gas flow path provided adjacent to cathode; power supply unit configured to supply electric power to stack; voltage sensor configured to detect stack voltage; temperature sensor configured to detect stack temperature; and control unit including processor and memory and configured to control power supply unit. Control unit controls power supply unit so that stack voltage becomes equal to or lower than upper limit value of stack voltage predetermined corresponding to stack temperature based on stack voltage detected by voltage sensor and stack temperature detected by temperature sensor during startup period until stack temperature reaches predetermined temperature after starting supply of electric power from power supply unit to stack.

Abstract: CO2 electrolysis apparatus includes: electrolysis stack configured to perform electrolysis using electric power generated by renewable energy; CO2 supply unit configured to supply CO2 to electrolysis stack; first storage unit configured to store first gas generated by electrolysis in electrolysis stack when CO2 is supplied; second storage unit configured to store second gas generated by electrolysis in electrolysis stack when supply of CO2 is stopped; reactor to which first and second gas stored in first and second storage unit are guided; voltage sensor configured to detect voltage of electrolysis stack; and control unit including processor and memory and configured to control CO2 supply unit to supply CO2 to electrolysis stack when detected voltage exceeds predetermined value and configured to control CO2 supply unit to stop supply of CO2 when detected voltage is equal to or less than predetermined value.

Abstract: The present invention provides an imidazo[1,2-a]pyridine compound that is excellent in pest control activity, particularly, insecticidal activity and/or acaracidal activity, is excellent in safety, and may be industrially advantageously synthesized. The imidazo[1,2-a]pyridine compound of the present invention is a compound of any of formulae (I) to (III) or a salt thereof.

Abstract: A compound represented by a formula (I) or a salt thereof: wherein A1 represents CR1 or a nitrogen atom; A2 represents CR2 or a nitrogen atom; A3 represents CR3 or a nitrogen atom, provided that two or more of A1 to A3 do not represent nitrogen atoms at the same time; R1, R2 and R3 each independently represent a hydrogen atom or the like; B1 represents CH or a nitrogen atom; R4 represents a substituted or unsubstituted C1-6 alkyl group or the like; R5 represents a substituted or unsubstituted C1-6 alkylthio group or the like; and R6 represents a substituted or unsubstituted C1-6 alkyl group or the like.

Abstract: A compound represented by Formula (I), or a salt thereof: wherein, R1 represents an unsubstituted or substituted C1-6 alkylthio group, or the like; A1 represents a nitrogen atom or CH; A2 represents a nitrogen atom or CR2; R2 and R3 each independently represents a hydrogen atom, an unsubstituted or substituted C6-10 aryl group, an unsubstituted or substituted 3- to 6-membered heterocyclyl group, or the like; B1 and B2 each independently represents a nitrogen atom or CR5, with the proviso that B1 and B2 do not represent CR5 at the same time, wherein R5 represents a hydrogen atom, an unsubstituted or substituted C1-6 alkyl group, or the like; R4 represents an unsubstituted or substituted C1-6 alkyl group, or the like, and R4 binds to any one of nitrogen atoms forming an imidazole ring or a triazole ring; and Ar represents an unsubstituted or substituted C6-10 aryl group or the like.

Abstract: An object of the present invention is to provide a heteroaryl azole compound that is excellent in pest control activity, particularly, insecticidal activity and/or miticidal activity, is excellent in safety, and may be industrially advantageously synthesized. The compound of the present invention is a compound represented by the formula (I), an N-oxide compound, stereoisomer, tautomer or hydrate thereof or a salt of any of these compounds. In the formula (I), A represents CH or a nitrogen atom; B1 represents CX1 or a nitrogen atom; X1, X2 and X3 each independently represent a hydrogen atom, a substituted or unsubstituted C1-6 alkyl group, a substituted or unsubstituted C2-6 alkenyl group, or the like; R1 represents a substituted or unsubstituted C1-6 alkylthio group, a substituted or unsubstituted C1-6 alkylsulfinyl group, or the like; R2 represents a substituted or unsubstituted C1-6 alkyl group; and R represents a substituted or unsubstituted C1-6 alkyl group.

Abstract: An object of the present invention is to provide a (hetero)aryl imidazole compound that is excellent in pest control activity, particularly, insecticidal activity and/or acaricidal activity, is excellent in safety, and may be industrially advantageously synthesized. The (hetero)aryl imidazole compound of the present invention is a compound represented by the formula (I) an N-oxide compound, stereoisomer, tautomer or hydrate thereof or a salt of any of these compounds. In the formula (I), B1 represents a nitrogen atom or CH; X represents a substituted or unsubstituted C3-8 cycloalkyl group; R1 represents a substituted or unsubstituted C1-6 alkylthio group or a substituted or unsubstituted C1-6 alkylsulfonyl group; R2 represents a substituted or unsubstituted C1-6 alkyl group; and R represents a substituted or unsubstituted C2-6 alkenyl group.

Abstract: A compound represented by Formula (I), or a salt thereof: wherein, R1 represents an unsubstituted or substituted C1-6 alkylthio group, or the like; A1 represents a nitrogen atom or CH; A2 represents a nitrogen atom or CR2; R2 and R3 each independently represents a hydrogen atom, an unsubstituted or substituted C6-10 aryl group, an unsubstituted or substituted 3- to 6-membered heterocyclyl group, or the like; B1 and B2 each independently represents a nitrogen atom or CR5, with the proviso that B1 and B2 do not represent CR5 at the same time, wherein R5 represents a hydrogen atom, an unsubstituted or substituted C1-6 alkyl group, or the like; R4 represents an unsubstituted or substituted C1-6 alkyl group, or the like, and R4 binds to any one of nitrogen atoms forming an imidazole ring or a triazole ring; and Ar represents an unsubstituted or substituted C6-10 aryl group or the like.

Abstract: A heteroaryl azole compound of the following formula (II): an N-oxide compound, stereoisomer, tautomer or hydrate thereof, or a salt of any of these compounds. In the formula (II), R1 represents a substituted or unsubstituted C1-6 alkylthio group or the like; B1 represents a nitrogen atom or CR2; R2 represents a hydrogen atom, a substituted or unsubstituted C1-6 alkyl group or the like; R3 represents a hydrogen atom, a substituted or unsubstituted C1-6 alkyl group or the like; R represents a substituted or unsubstituted C1-6 alkyl group or the like; A represents a carbon atom or a nitrogen atom; X represents a substituted or unsubstituted C1-6 alkyl group or the like; n represents a number of chemically acceptable X, and is an integer of 0 to 2; and X is the same or different when n is 2.

Abstract: A compound represented by a formula (I) or a salt thereof: wherein A1 represents CR1 or a nitrogen atom; A2 represents CR2 or a nitrogen atom; A3 represents CR3 or a nitrogen atom, provided that two or more of A1 to A3 do not represent nitrogen atoms at the same time; R1, R2 and R3 each independently represent a hydrogen atom or the like; B1 represents CH or a nitrogen atom; R4 represents a substituted or unsubstituted C1-6 alkyl group or the like; R5 represents a substituted or unsubstituted C1-6 alkylthio group or the like; and R6 represents a substituted or unsubstituted C1-6 alkyl group or the like.

Abstract: A compound represented by Formula (I), or a salt thereof: wherein, R1 represents an unsubstituted or substituted C1-6 alkylthio group, or the like; A1 represents a nitrogen atom or CH; A2 represents a nitrogen atom or CR2; R2 and R3 each independently represents a hydrogen atom, an unsubstituted or substituted C6-10 aryl group, an unsubstituted or substituted 3- to 6-membered heterocyclyl group, or the like; B1 and B2 each independently represents a nitrogen atom or CR5, with the proviso that B1 and B2 do not represent CR5 at the same time, wherein R5 represents a hydrogen atom, an unsubstituted or substituted C1-6 alkyl group, or the like; R4 represents an unsubstituted or substituted C1-6 alkyl group, or the like, and R4 binds to any one of nitrogen atoms forming an imidazole ring or a triazole ring; and Ar represents an unsubstituted or substituted C6-10 aryl group or the like.