| 序号 | 专利名 | 申请号 | 申请日 | 公开（公告）号 | 公开（公告）日 | 发明人 |
|---|---|---|---|---|---|---|
| 121 | Fluorinated thiocarbonic acid ester-fluoride | JP23769984 | 1984-11-13 | JPS60123464A | 1985-07-02 | EERITSUHI KURAUKE; ENGERUBERUTO KIYUURE |
| 122 | JPS609748B2 - | JP11416078 | 1978-09-19 | JPS609748B2 | 1985-03-12 | REIMONDO ANTONII FUERITSUKUSU |
| 123 | Substituted 2-nitro-5-(4-trifluoromethyl- phenoxy)-toluenes, manufacture and use as herbicide and plant growth regulant | JP18304982 | 1982-10-20 | JPS58109448A | 1983-06-29 | HAINTSU FUERUSUTAA; RUUTOUITSUHI OIE; ROBERUTO SHIYUMITSUTO; KURAUSU RIYURUSEN |
| 124 | Manufacture of chlorothiol formic acid ester | JP6633080 | 1980-05-19 | JPS5620567A | 1981-02-26 | JIEEMUSU ARISON KUTSUKU JIYUNI; UIRIAMU ARUBAATO KEIN |
| 125 | Novel anthraquinone compound | JP9432679 | 1979-07-26 | JPS5519295A | 1980-02-09 | JIAN MARII ADAMU |
| 126 | 1*22dicyclocyanovinyl compound*microbe controlling method utilizing said compound and composition containing it | JP11416078 | 1978-09-19 | JPS5452030A | 1979-04-24 | REIMONDO ANTONII FUERITSUKUSU |
| 127 | Killing active 1*33benzodithioll22thion compound | JP9576878 | 1978-08-04 | JPS5448761A | 1979-04-17 | KARITSUDO RASHIIDO; JIEIMUZU DEI WAAKENCHIN |
| 128 | Preparation of dibenzyltrithiocarbonate | JP2002077 | 1977-02-24 | JPS53105450A | 1978-09-13 | TADA NOBUO; ASAOKA TSUTOMU; HATANAKA TSUTOMU; WACHI TOSHIO |
| PURPOSE: To prepare the title cpd., useful as lubricant additives and agrichemicals, by reaction of a specific aq. soln. of sodium sulfide with carbon disulfide, followed by reaction with benzyl chloride. COPYRIGHT: (C)1978,JPO&Japio | ||||||
| 129 | Process for proparing vinyl isochoroformate and thiochloroformate and resulting product | JP1995678 | 1978-02-24 | JPS53105427A | 1978-09-13 | PITOO MARUKU DANIERU ARUSEENU; MARUFURUUTO TEIERII ANDORE |
| 130 | Novel phenol process for preparing same and stabilized organic material containing same | JP4311277 | 1977-04-14 | JPS52128359A | 1977-10-27 | SAMIYUERU EBANSU |
| 131 | JPS5130055B1 - | JP4455664 | 1964-08-05 | JPS5130055B1 | 1976-08-30 | |
| 132 | JPS4975527A - | JP11886173 | 1973-10-22 | JPS4975527A | 1974-07-20 | |
| 133 | 化合物、連鎖移動剤、及び高分子の製造方法 | JP2019011490 | 2019-01-25 | JP2020117643A | 2020-08-06 | 三浦 佳子; 長尾 匡憲; 星野 友 |
| 【課題】水溶性に優れ、連鎖移動剤として使用可能な化合物を提供すること。 【解決手段】本開示の連鎖移動剤は、末端に2つの水酸基、アミド基、または、両末端にアミド基を有するトリチオカルボニル化合物であり、一例として下記一般式(1)、(2)で表される。 一般式(1)中、L1は、アミド基、メチレン基、又は炭素数2〜10のアルキレン基を示し、該アルキレン基を構成するメチレン基の少なくとも一つがアミド基で置換されていてもよい。一般式(2)中、L2は、直接結合、メチレン基、又は炭素数2〜10のアルキレン基を示し、メチレン基の少なくとも一つがアミド基で置換されていてもよい。 【選択図】なし |
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| 134 | ジベンジルトリチオカーボネート誘導体およびその製造方法 | JP2013088331 | 2013-04-19 | JP2014210738A | 2014-11-13 | HATANO TAKASHI; MORI TOSHIKI; TANAKA SHIMON; NAGATA FUMIO; SHIGEMATSU MASAMI |
| 【課題】分子の両末端に種々の官能基を有するジベンジルトリチオカーボネート誘導体およびその製造方法を提供する。【解決手段】以下の、一般式(1):[式中、Arはフェニレンまたはナフチレン基であり、Rは、アセトキシ、ヒドロキシもしくはヒドロキシメチル基であるか、または式−C(O)−O−CH2−R1(ここで、R1は置換基を有するC1〜C5アルキルまたはC2〜C5アルケニル基である)で表される、置換基を有するメトキシカルボニル基である]で表されるジベンジルトリチオカーボネート誘導体。[式中、Xはハロゲン原子である]で表される化合物を、アミド系溶媒中、トリチオ炭酸塩と反応させてトリチオカーボネート化することを特徴とする一般式(1)で表されるジベンジルトリチオカーボネート誘導体の製造方法。【選択図】なし | ||||||
| 135 | Chain transfer agent, and method for producing block copolymer | JP2013001962 | 2013-01-09 | JP2014133801A | 2014-07-24 | INADA MASAYOSHI; MOGAMI HIROKAZU |
| PROBLEM TO BE SOLVED: To provide a chain transfer agent with which various kinds of block copolymers are produced without being restricted by kinds of raw material monomers, with which a polymerization condition of the block copolymers is easily controlled, and which is obtained by a comparatively simple synthetic method, and to provide a method for producing the block copolymers.SOLUTION: A chain transfer agent is used for a reversible addition cleavage chain transfer polymerization, has a structure represented by general formula (1) at the end thereof, and is a di- or tri-thiocarbonate in which the structure is bound to a carbon atom or to a sulfur atom. In a method for producing a block copolymer, at least one of an acrylic ester, a methacrylic ester, and an aromatic vinyl compound is subjected to the reversible addition cleavage chain transfer polymerization by using the chain transfer agent. In formula (1), Ris a hydrogen atom or a 1-6C alkyl group. | ||||||
| 136 | Dibenzyl trithiocarbonate derivative, its production method and a polymer using the same | JP2006056779 | 2006-03-02 | JP5016829B2 | 2012-09-05 | 寛 津田; 俊紀 藤井; 剛 遠藤; 直人 青柳 |
| 137 | Use is produced polymers and of these by the use of sulfur compounds in the form of a transfer agent for the radical polymerization, which is control of the acrylic acid | JP2007523097 | 2005-03-23 | JP4964132B2 | 2012-06-27 | ジヤツクメ，クリスチアン; スユオ，ジヤン−マルク |
| 138 | Initiators for the controlled radical polymerization, S as chain transfer agents or chain terminators, S'-bis - (α, α'- disubstituted-alpha "- acetic acid) - trithiocarbonate compounds and derivatives thereof, and process for their preparation | JP2001559843 | 2001-01-11 | JP4914553B2 | 2012-04-11 | ジョン・ティー・ライ |
| 139 | Synthesis of trithiocarbonate raft agents and their intermediates | JP2007513342 | 2005-05-11 | JP4733696B2 | 2011-07-27 | ブラウン ファーナム ウィリアム |
| 140 | Trithiocarbonate compound and method for producing the same | JP2009049177 | 2009-03-03 | JP2010202572A | 2010-09-16 | MATSUSHITA AKIO; YOSHII KIYOTAKA; MORIGAMI ATSUSHI |
| <P>PROBLEM TO BE SOLVED: To provide an industrially inexpensive and simple production method of a new trithiocarbonate compound. <P>SOLUTION: The trithiocarbonate compound is represented by general formula (1) (wherein R is an optionally substituted 1-20C hydrocarbon group optionally containing a heteroatom or a cyclic structure in its carbon chain). The trithiocarbonate compound represented by general formula (1) is produced by causing a dithiol to react with carbon disulfide under a basic condition and subsequently with an allyl halide. <P>COPYRIGHT: (C)2010,JPO&INPIT | ||||||
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