Abstract: A first tank, a main body of a compressor, an electric motor, and a second tank are combined to form a single assembly. A booster type air compressor as the single assembly including the first tank may be easily carried. The first tank at an inlet side is integrally combined to prevent a pulsation in the supplied compressed air for eliminating the drain contained in the compressed air. The air compressor, thus, is structured to discharge high compressed air from a high-pressure outlet joint formed on the second tank.

Abstract: The present invention relates to a novel production method of a diaminopyrimidine compound useful as an intermediate for various compounds having a pharmacological activity, a novel intermediate useful for producing said compound, and a production method of the intermediate. The present invention provides a novel 5-aminopyrimidine compound represented by the following formula (2) and a novel 4,5-diaminopyrimidine compound represented by the formula (3), as well as production methods of the compounds of the following formulas (2) to (6). wherein each symbol is as defined in the specification.

Abstract: There is provided methods for producing nateglinide crystals, which comprises the steps of adding an acid(s) to a reaction mixture containing nateglinide to make it acidic, the reaction mixture being obtained by reacting trans-4-isopropylcyclohexylcarbonyl chloride with D-phenylalanine in a mixed solvent of ketone solvent and water in the presence of an alkali; and then adjusting the temperature of the mixture to 58° C. to 72° C. and the concentration of ketone solvent to more than 8 wt % and less than 22 wt % to conduct precipitation of nateglinide crystals. This producing method is the industrially beneficial methods for crystallization of nateglinide.

Abstract: The present invention relates to a technique of amplifying a target nucleic acid contained in a specimen, and further to a technique of analyzing the amplified target nucleic acid. The present invention provides a nucleic acid amplification container (3) to be installed in a nucleic acid analyzing apparatus when used. The nucleic acid amplification container (3) includes a container main body (30) having a reactor (34) where the target nucleic acid and an amplification reagent are to be reacted, and a cap (31) that covers an upper opening of the reactor (34) and can be completely separated from the container main body (30).

Abstract: Compounds represented by formula (II): wherein M is a hydrogen atom, sodium, potassium, or lithium; P is a hydrogen atom, an alkyl group, and the like; and the wavy line indicates a cis form, a trans form, or a mixture thereof for the double bond to which it is attached, may be prepared by hydrolyzing a compound represented by formula (I), or a salt thereof: wherein R1 and R2 are the same or different and each is an alkyl group, or R1 and R2 together with the adjacent nitrogen atom may form an aliphatic heterocycle, and P and the wavy line are as defined above, in the presence of alkali metal hydroxide.

Abstract: In an audio signal processing device which processes audio signals and outputs the audio signals, on the recalling setting data representing a setting status of the device, protection setting defining a group which is not recalled at the time of recalling the setting data among a plurality of groups constituting the setting data is accepted as a local setting for each setting data and a global setting common to each setting data separately, and an enabled or disabled setting of the protection setting for the setting data is accepted for each setting data, wherein when the setting data is recalled, the recall is performed in accordance with the local protection setting when the protection setting for the setting data is enabled, and in accordance with the global protection setting when the protection setting for the setting data is disabled.

Abstract: A dibenzylamine compound represented by the formula (1) wherein R1 and R2 are each a C1-6 allyl group optionally substituted by halogen atoms and the like; R3, R4 and R5 are each a hydrogen atom, a halogen atom and the like, or R3 and R4 may form, together with carbon atoms bonded thereto, a homocyclic or heterocyclic ring optionally having substituent(s); A is —N(R7)(R8) and the like; ring B is an aryl group or a heterocyclic residue; R6 is a hydrogen atom, a halogen atom, a nitro group, a C1-6 allyl group and the like; n is an integer of 1 to 3, a prodrug thereof and a pharmaceutically acceptable salt thereof show selective and potent CETP inhibitory activity, and therefore, they can be provided as therapeutic or prophylactic agents for hyperlipidemia or arteriosclerosis and the like.

Abstract: Timer generates a first time code with a relatively high resolution. Second time code, given from a reproduction device in relation to video or music reproduced by the reproduction device, has a resolution lower than the first time code. By correcting the timer-generated first time code on the basis of the second time code, there can be generated a corrected first time code having a same over-time progression as the second time code but having a higher resolution than the second time code. Once an operator, such as a mixer, is operated at given reproduction timing of the video or music during recording, data indicative of the operation is stored in a memory along with the first time code corrected in accordance with the second time code. In reproduction, the memory is read in accordance with the first time code, corrected on the basis of the second time code.

Abstract: A magnetic tape cartridge has a case including a datum hole into which a positioning pin is inserted at a predetermined position thereof; a reel rotatably supported on the case with a magnetic tape wound thereon and including an engaging gear formed in the outer periphery of the flange thereof; a rotation restricting mechanism disposed in the case and engaging with the engaging gear of the reel to thereby restrict the rotation of the reel; and, an engagement releasing element slidably inserted into the datum hole from inside the case and removing the engagement between the rotation restricting mechanism and the engaging gear through the sliding movement thereof within the datum hole, wherein the positioning pin is inserted into the datum hole from outside of the case and push and slide the engagement releasing element, thereby releasing the rotation restriction of the reel by the rotation restricting mechanism.

Abstract: Compounds represented by formula (II): wherein M is a hydrogen atom, sodium, potassium, or lithium; P is a hydrogen atom, an alkyl group, and the like; and the wavy line indicates a cis form, a trans form, or a mixture thereof for the double bond to which it is attached, may be prepared by hydrolyzing a compound represented by formula (I), or a salt thereof: wherein R1 and R2 are the same or different and each is an alkyl group, or R1 and R2 together with the adjacent nitrogen atom may form an aliphatic heterocycle, and P and the wavy line are as defined above, in the presence of alkali metal hydroxide.

Abstract: A power source system to be mounted in electrical devices is provided. The power source system includes a fuel cell which supplies electric power generated by consuming fuel, a fuel storage portion which stores the fuel and supplies the fuel to the fuel cell, a container which contains the fuel cell and the fuel storage portion, and a case which is provided so as to surround the container. A space for allowing air used for the reaction in the fuel cell to circulate therethrough is provided between the container and the case.

Abstract: A production method for conveniently producing a 5?-acyloxynucleoside compound shown by the formula [A] in a good yield while suppressing formation of by-products, including subjecting a 2?,3?,5?-triacyloxynucleoside compound represented by the formula [I] to selective deacylation in an alcohol represented by the formula [II] using a base selected from the group consisting of alkali metal hydroxide, alkali metal alkoxide and alkali metal carbonate: wherein each symbol in the formula is as defined in the specification.

Abstract: A dibenzylamine compound represented by the formula (1) wherein R1 and R2 are each a C1-6 alkyl group optionally substituted by halogen atoms and the like; R3, R4 and R5 are each a hydrogen atom, a halogen atom and the like, or R3 and R4 may form, together with carbon atoms bonded thereto, a homocyclic or heterocyclic ring optionally having substituent(s); A is —N(R7) (R8) and the like; ring B is an aryl group or a heterocyclic residue; R6 is a hydrogen atom, a halogen atom, a nitro group, a C1-6 alkyl group and the like; n is an integer of 1 to 3, a prodrug thereof and a pharmaceutically acceptable salt thereof show selective and potent CETP inhibitory activity, and therefore, they can be provided as therapeutic or prophylactic agents for hyperlipidemia or arteriosclerosis and the like.

Abstract: Compound (II) is reacted with formate in the presence of an alkali metal alkoxide and the like to give compound (III); then this is reacted with compound (IVa) or compound (IVb) to give compound (V); then this is reacted with compound (VI) to give compound (VII); and then this is deprotected to give compound (I). The present invention provides an industrially advantageous production method of a 4-acetylpyrimidine compound useful as a synthetic intermediate for a pharmaceutical product: wherein X is a methylthio group and the like, R1 is a lower alkyl group and the like, R2 is a lower alkyl group optionally having substituent(s) and the like, M is an alkali metal and X1 is a halogen atom.

Abstract: Compound (II) and compound (III) are reacted to give compound (IVa) and/or compound (IVb); which are/is then reacted with compound (V) to give compound (I). wherein X is a methylthio group and the like, R1 and R2 are each a lower alkyl group optionally having substituent(s), an aryl group optionally having substituent(s) and the like, R3 is a lower alkyl group, R4 is a hydrogen atom, a lower alkyl group optionally having substituent(s) and the like, and Q is a carboxylate group and the like.

Abstract: The recording medium cartridge includes a cartridge case containing a recording medium and a noncontact-type memory having an IC section for storing information and performing signal processing and an antenna section for transmitting and receiving signals. The antenna section of the memory is placed in a region furthest from metallic parts.

Abstract: A magnetic tape cartridge is equipped with a cartridge, a single tape reel, a tape leader pin, and a U-shaped clip. The cartridge case is formed by fastening upper and lower cases of synthetic resin together and has a tape leader opening formed in the upper and lower side walls of the upper and lower cases. The single tape reel has magnetic tape wound thereon and is rotatably housed within the cartridge case. The tape leader pin is firmly attached to a leading end of the magnetic tape, and is detachably held in an upright state between the upper and lower cases so that it faces the tape leader opening. The U-shaped clip is attached to walls near the tape leader opening to fasten the upper and lower cases together, whereby the fastening strength of the upper and lower cases is enhanced.

Abstract: There is provided methods for producing nateglinide crystals, which comprises the steps of adding an acid(s) to a reaction mixture containing nateglinide to make it acidic, the reaction mixture being obtained by reacting trans-4-isopropylcyclohexylcarbonyl chloride with D-phenylalanine in a mixed solvent of ketone solvent and water in the presence of an alkali; and then adjusting the temperature of the mixture to 58° C. to 72° C. and the concentration of ketone solvent to more than 8 wt % and less than 22 wt % to conduct precipitation of nateglinide crystals. This producing method is the industrially beneficial methods for crystallization of nateglinide.