利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

45 条记录 (耗时 0.031 秒)

    Photosensitive composition and photosensitive lithographic printing plate
    2.
    发明授权
    Photosensitive composition and photosensitive lithographic printing plate 失效
    感光组合物和感光平版印刷版

    公开(公告)号：US5645969A

    公开(公告)日：1997-07-08

    申请号：US576136

    申请日：1995-12-21

    申请人： Fumiyuki Matsuo ,  Daisuke Kanazawa ,  Mitsuru Sasaki ,  Shinichi Matsubara ,  Katsuhiko Higashino ,  Toshiaki Yokoo

    发明人： Fumiyuki Matsuo ,  Daisuke Kanazawa ,  Mitsuru Sasaki ,  Shinichi Matsubara ,  Katsuhiko Higashino ,  Toshiaki Yokoo

    IPC分类号： G03F7/023

    CPC分类号： G03F7/0236

    摘要： A photosensitive composition comprising a quinonediazide compound and a binder resin, wherein said resin is a resin obtained by condensing a phenol component comprising the following (1) to (3), and an aldehyde or a ketone, and X.gtoreq.0.57, where X=A/B, where A is an integrated value of peaks from 23.0 to 31.0 ppm, and B is an integrated value of peaks from 23.0 to 37.0 ppm, in the .sup.13 C-NMR spectrum of a dimethyl sulfoxide deuteride solution of this resin:Phenol Component(1) a phenol: from 50 to 100 mol %(2) a m-alkylphenol: from 0 to 50 mol %(3) a p-alkylphenol: from 0 to 50 mol %

    摘要翻译： 一种包含醌二叠氮化合物和粘合剂树脂的光敏组合物，其中所述树脂是通过将包含下列（1）至（3）的苯酚组分与醛或酮缩合得到的树脂，X> = 0.57，其中 X = A / B，其中A为23.0至31.0ppm的峰的积分值，B为23.0至37.0ppm的峰的积分值，该树脂的二甲基亚砜氘化物溶液的13 C-NMR光谱： 苯酚成分（1）苯酚：50〜100摩尔％（2）间 - 烷基苯酚：0〜50摩尔％（3）对烷基酚：0〜50摩尔％

    Method for forming a positive image
    3.
    发明授权
    Method for forming a positive image 有权
    形成正像的方法

    公开(公告)号：US06399279B1

    公开(公告)日：2002-06-04

    申请号：US09232727

    申请日：1999-01-19

    申请人： Toshiyuki Urano ,  Etsuko Hino ,  Mitsuru Sasaki

    发明人： Toshiyuki Urano ,  Etsuko Hino ,  Mitsuru Sasaki

    IPC分类号： G03F732

    CPC分类号： G03F7/322 ,  B41C1/1008 ,  B41C2210/02 ,  B41C2210/06 ,  B41C2210/22 ,  B41C2210/262

    摘要： A method for forming a positive image, which comprises exposing an image-forming material comprising a substrate and a positive photosensitive composition layer containing a novolak resin and a photo-thermal conversion material which absorbs light from an image exposure light source and converts it to heat and not containing a thermally decomposable material which decomposes by the action of heat generated by the photo-thermal conversion material upon absorption of light from the image exposure light source, formed on the substrate, followed by development with an alkali developer containing an amphoteric surfactant to form a positive image.

    摘要翻译： 一种用于形成正像的方法，其包括曝光包含基底的图像形成材料和含有酚醛清漆树脂的正性感光性组合物层和从图像曝光光源吸收光的光热转换材料，并将其转换成热 并且不含有通过在形成于基板上的来自图像曝光光源的光吸收时由光热转换材料产生的热的作用而分解的热分解材料，然后用含有两性表面活性剂的碱性显影剂显影， 形成积极的形象。

    Navigation system, portable terminal device, and in-vehicle device
    5.
    发明授权
    Navigation system, portable terminal device, and in-vehicle device 有权
    导航系统，便携式终端设备和车载设备

    公开(公告)号：US08442768B2

    公开(公告)日：2013-05-14

    申请号：US12738893

    申请日：2008-10-22

    申请人： Mitsuru Sasaki

    发明人： Mitsuru Sasaki

    IPC分类号： G01C21/34 ,  G01C21/30 ,  G01C21/32 ,  G08G1/123

    CPC分类号： G08G1/0969 ,  G01C21/26 ,  G01C21/3688

    摘要： A navigation system is configured such that: an in-vehicle device collects and provides position information and movement information of a vehicle to a portable terminal device, and displays image data sent from the portable terminal device. The portable terminal device acquires map information from a map center device based on the position information and the movement information sent from the in-vehicle device, calculates an actual location of the vehicle based on the position information and the movement information sent from the in-vehicle device, and generates image data in which the calculated actual location is superposed on the acquired map information.

    摘要翻译： 导航系统被配置为使得：车载设备向便携式终端设备收集并提供车辆的位置信息和移动信息，并且显示从便携式终端设备发送的图像数据。 便携式终端装置基于从车载装置发送的位置信息和移动信息，从地图中心装置获取地图信息，基于从内线装置发送的位置信息和移动信息，计算出车辆的实际位置， 并且生成其中所计算的实际位置叠加在所获取的地图信息上的图像数据。

    Thiophosphoric acid ester as a soil pest controlling agent
    7.
    发明授权
    Thiophosphoric acid ester as a soil pest controlling agent 失效
    硫代磷酸酯作为土壤虫害防治剂

    公开(公告)号：US4940699A

    公开(公告)日：1990-07-10

    申请号：US344409

    申请日：1989-04-28

    申请人： Yoshikazu Itoh ,  Makoto Hatakoshi ,  Mitsuru Sasaki

    发明人： Yoshikazu Itoh ,  Makoto Hatakoshi ,  Mitsuru Sasaki

    IPC分类号： A01N57/12 ,  C07F9/165

    CPC分类号： A01N57/12 ,  C07F9/1651

    摘要： The present invention relates to an O,O-diethyl O-1-(N-methoxyimino)ethyl thiophosphonate and O,O-diethyl O-1-(N-methoxyimino)-propyl thiophosphate useful to control pests living in soil. Said compounds have an excellent activity in controlling pests living in soil such as southern corn rootworm, cupreous chafer etc.

    摘要翻译： 本发明涉及用于控制生活在土壤中的害虫的O，O-二乙基O-1-（N-甲氧基亚氨基）乙基硫代膦酸酯和O，O-二乙基O-1-（N-甲氧基亚氨基） - 丙基硫代磷酸酯。 所述化合物在控制生活在土壤中的害虫，如南方玉米根虫，铜箔胎圈包布等方面具有优异的活性。

    Aluminum phosphinate-amine adducts, and their production and use
    8.
    发明授权
    Aluminum phosphinate-amine adducts, and their production and use 失效
    铝次膦酸胺加合物及其生产和使用

    公开(公告)号：US4701209A

    公开(公告)日：1987-10-20

    申请号：US865967

    申请日：1986-05-22

    申请人： Mitsuru Sasaki ,  Yukio Oguri

    发明人： Mitsuru Sasaki ,  Yukio Oguri

    IPC分类号： C07F9/32 ,  A01N57/20 ,  C07C67/00 ,  C07C209/00 ,  C07C211/01 ,  C07F9/48 ,  C07F5/06 ,  A01N55/02

    CPC分类号： A01N57/20 ,  C07F9/4816

    摘要： Aluminum phosphinate-amine adducts of the formula: ##STR1## wherein R.sub.1, R.sub.2 and R.sub.3 are each a hydrogen atom, a lower alkyl group, a lower alkoxy(lower)alkyl group, a lower alkylthio(lower)alkyl group or a cyclo(lower)alkyl group to aluminum 1-hydroxyethylphosphinate-amine, which are useful for prevention and treatment of plant diseases caused by phytopathogenic fungi.

    摘要翻译： 具有下式的铝次膦酸盐 - 胺加合物：其中R 1，R 2和R 3各自为氢原子，低级烷基，低级烷氧基（低级）烷基，低级烷硫基（低级）烷基或低级烷硫基 一个环（低级）烷基至1-羟乙基次膦酸铝 - 胺，可用于预防和治疗由植物病原真菌引起的植物病害。

    Preparation of 5-methyl-2-nitrophenol
    9.
    发明授权
    Preparation of 5-methyl-2-nitrophenol 失效
    制备5-甲基-2-硝基苯酚

    公开(公告)号：US4034050A

    公开(公告)日：1977-07-05

    申请号：US641585

    申请日：1975-12-17

    申请人： Mitsuru Sasaki ,  Kunio Mukai

    发明人： Mitsuru Sasaki ,  Kunio Mukai

    IPC分类号： C07C205/22 ,  C07F9/12 ,  C07C79/24

    CPC分类号： C07C201/12 ,  C07F9/12

    摘要： Process for preparing 5-methyl-2-nitrophenol of high purity by sulfonating tri-m-cresyl phosphate, nitrating the sulfonated tri-m-cresyl phosphate, hydrolyzing the nitrated, sulfonated tri-m-cresyl phosphate to obtain a mixture of nitro-m-cresols, steam-distilling the mixture, and repeatedly washing the distillate with a dilute aqueous alkaline solution.

    摘要翻译： 通过磺化三间甲酚磷酸盐，硝化磺化三间甲酚磷酸盐，水解硝化磺化三间甲酚磷酸盐得到硝基苯酚的混合物，制备高纯度的5-甲基-2-硝基苯酚的方法， m-甲酚，蒸汽蒸馏混合物，并用稀碱性碱溶液反复洗涤馏出物。

    BENZAZEPINE DERIVATIVES AND THEIR USE AS HISTAMINE H3 ANTAGONISTS
    10.
    发明申请
    BENZAZEPINE DERIVATIVES AND THEIR USE AS HISTAMINE H3 ANTAGONISTS 审中-公开

    公开(公告)号：US20110124626A1

    公开(公告)日：2011-05-26

    申请号：US13054688

    申请日：2009-07-17

    申请人： Parminder Kaur Pooni ,  Kevin John Merchant ,  Catrina Morvern Kerr ,  Stuart Richard Crosby ,  Tomohiro Okawa ,  Mitsuru Sasaki ,  Mika Gotou ,  Graham Andrew Showell ,  Martin Richard Teall

    发明人： Parminder Kaur Pooni ,  Kevin John Merchant ,  Catrina Morvern Kerr ,  Stuart Richard Crosby ,  Tomohiro Okawa ,  Mitsuru Sasaki ,  Mika Gotou ,  Graham Andrew Showell ,  Martin Richard Teall

    IPC分类号： A61K31/397 ,  C07D403/12 ,  A61K31/55 ,  C07D401/12 ,  C07D223/16 ,  C07D413/10 ,  C07D403/14 ,  A61P25/28

    CPC分类号： C07D403/12 ,  C07D223/16 ,  C07D401/06 ,  C07D401/12 ,  C07D401/14 ,  C07D405/12 ,  C07D405/14 ,  C07D409/12 ,  C07D409/14 ,  C07D413/12 ,  C07D417/12

    摘要： A compound having the formula (1) wherein: R1 is a group selected from C3-8 cycloalkyl, C1-6 alkyl, C1-6 alkylene-C3-8 cycloalkyl, each of which groups may optionally be substituted with C1-6 alkyl, halogen, haloC1-6 alkyl or OR15, or R1 is heterocyclyl, optionally substituted with C1-6 alkyl, haloC1-6 alkyl or OR15; n is 0, 1, 2, 3 or 4, the alkylene group —(CH2)m— formed thereby being optionally substituted with a group selected from C1-4 alkyl, C3-8 cycloalkyl and arylsulfonyl; A is a group selected from —N(R2)CO—, —CON(R2)-, —OC(O)—, —C(O)O—, —CO—, —C(R2)(OR3)-, —C(═N—O—R3)-, —C(═CR2R3)-, —C3-8 cycloalkylene-, —C(R2)(haloC1-6alkyl)-, C1-4 alkylene and —C(OR3)(haloC1-6alkyl)-; R2 and R3 are each independently selected from H, C1-6 alkyl, and C3-8 cycloalkyl, or, when A is —N(R2)CO— and X is absent, R2 may form, together with the adjacent nitrogen atom and Z, an N-containing heterocyclyl group, which may optionally be substituted; X is absent or is C14 alkylene or C24 alkenylene, each of which may optionally be substituted with one or more C1-4 alkyl groups, OR16, halogen or haloC1-6 alkyl; Z is selected from aryl, heteroaryl, C3-8 cycloalkyl, and heterocyclyl, each of which may optionally be substituted by a group selected from —Y-aryl, heteroaryl, —Y—C3-8 cycloalkyl and —Y-heterocyclyl, or, when X is present, Z may be H, or, when X is absent and A is —C(R2)(OR3)- or —N(R2)CO—, Z may be H, or, when A is —N(R2)CO— and X is absent, Z may form, together with the adjacent nitrogen atom and R2, an N-containing heterocyclyl group which may optionally be substituted, wherein, when A is —CO—, Z is linked to X or A via a carbon atom and wherein, when A is —N(R2)CO— and Z is H, R1 is C3-8 cycloalkyl; and Y represents a bond, C1-6 alkylene, CO, NR14, COC2-6 alkenylene, O, SO2 or NHCOC1-6 alkylene; wherein said cycloalkyl, aryl, heteroaryl and heterocyclyl groups Z may be optionally substituted by one or more substituents which may be the same or different, and which are selected from halogen, haloC1-6 alkyl, hydroxy, cyano, nitro, ═O, —R4, —CO2R4, —COR4, —NR5R6, —C1-6 alkyl-NR5R6, —C3-8 cycloalkyl-NR5R6, —CONR12R13, —NR12COR13, —NR5SO2R6, —OCONR5R6, —NR5CO2R6, —NR4CONR5R6 or —SO2NR5R6-SHR8, -alkyl-OR8, —SOR8, —OR9, —SO2R9, —OSO2R9, -alkyl-SO2R9, -alkyl-CONHR9, -alkyl-SONHR9, -alkyl-COR10, —CO-alkyl-R10, —O-alkyl-R11 (wherein R4, R5 and R6 independently represent hydrogen, C1-6 alkyl, —C3-8 cycloalkyl, —C1-6 alkylene-C3-8 cycloalkyl, aryl, heterocyclyl or heteroaryl, wherein R8 represents C1-6 alkyl, wherein R9 represents C1-6 alkyl or aryl, wherein R10 represents aryl, wherein R11 represents C3-8 cycloalkyl or aryl, R12, R13, R14, R15 and R16 each independently represent H or C1-6 alkyl, and wherein —NR5R6 and —NR12R13 may represent a nitrogen containing heterocyclyl group); wherein said R4, R5, R6 R8, R9, R11 and R11 groups may be optionally substituted by one or more substituents which may be the same or different, and which are selected from the group consisting of halogen, hydroxy, C1-6 alkyl, C1-6 alkoxy, cyano, amino, ═O or trifluoromethyl; and wherein substituents of Z selected from —Y-aryl, —Y-heteroaryl, —Y—C3-8cycloalkyl and —Y-heterocyclyl may be optionally substituted by one or more substituents selected from ═O, hydroxy, cyano, nitro, halogen, haloC1-6 alkyl and C1-6alkyl; and wherein, when A is C1-4 alkylene, said cycloalkyl, aryl, heteroaryl or heterocyclyl group Z (such as a heterocyclyl group Z) is substituted at least with hydroxy, CF3, or ═O; and wherein, when A is CON(R2) n is 1; or a pharmaceutically acceptable salt or ester thereof, provided that: when A is —CO—, R1 is CH3, C3-8 cycloalkyl-substituted C1-6 alkylene or n-butyl, n is 0 and X is —CH2CH2—, Z is not N-benzyl substituted 4-piperidinyl, N-(3-fluorobenzyl)-substituted 4-piperidinyl or N-acetyl substituted 4-piperidinyl; when A is —OC(O)—, R1 is cyclobutyl, n is 0 and X is —CH2CH2—, Z is not H; when A is —OC(O)—, R1 is n-propyl, n is 0 and X is —CH2—, Z is not H; and when A is —CO—, R1 is CH3, n is 0 and X is CH2, Z is not H.