专利检索_硫氰酸或异硫氰酸的衍生物专利检索_硫氰酸或异硫氰酸的衍生物专利检索查询

子分类：

序号	专利名	申请号	申请日	公开（公告）号	公开（公告）日	发明人
1	光刻蚀法中使用的含噻吩的光酸生成剂	CN02812555.X	2002-06-06	CN1518684A	2004-08-04	李文杰; 普什卡拉·R·瓦拉纳西; 陈光军
具有任一下述通式的含噻吩的光酸生成剂，其中，R1、R2或R3中至少有一个是噻吩或被烷基、烷氧基或环烷基取代的噻吩，不含噻吩部分的其余R1、R2或R3独立地选自烷基、环烷基和芳基，或者R1、R2或R3中至少有一个结合在一起形成具有约4至约8个环碳原子的环状部分；Y是抗衡离子，本发明还公开了该光酸生成剂在化学放大的抗蚀剂组合物中的应用。
2	光刻蚀法中使用的含噻吩的光酸生成剂	CN02812555.X	2002-06-06	CN100432837C	2008-11-12	李文杰; 普什卡拉·R·瓦拉纳西; 陈光军
具有任一下述通式的含噻吩的光酸生成剂，其中，R1、R2或R3中至少有一个是噻吩或被烷基、烷氧基或环烷基取代的噻吩，不含噻吩部分的其余R1、R2或R3独立地选自烷基、环烷基和芳基，或者R1、R2或R3中至少有一个结合在一起形成具有约4至约8个环碳原子的环状部分；Y是抗衡离子，本发明还公开了该光酸生成剂在化学放大的抗蚀剂组合物中的应用。
3	制备烷氧羰基异硫氰酸酯的方法	CN201380052441.X	2013-10-09	CN104736517A	2015-06-24	J·S·菲斯克; D·C·布兰德; G·J·弗塞克
本申请提供由氯甲酸烷基酯和硫氰酸盐在甲苯中通过控制水和催化剂的量来制备烷氧羰基异硫氰酸酯的方法。
4	Container for preserving raw rice cake	JP34233393	1993-12-13	JPH07165273A	1995-06-27	MITA KOZO; YAMAZAKI TAKUYA
PURPOSE: To destroy the microorganisms occurring in raw rice cake and remove unpleasant, irritating odor at the time of unpacking by a method wherein an isothiocyanic acid ester vapor generating member, together with raw rice cake, is placed into a container and an isothiocyanic acid ester adsorbing sealant layer is provided on the inner surface of the container. CONSTITUTION: A preservation container 1 has a raw rice cake 20 intended for retention of its quality and an isothiocyanic acid ester vapor generating member 10 both contained in a packaging container 50 provided with an isothiocyanic acid ester adsorbing sealant layer 57. The isothiocyanic acid ester vapor generating member 10 consists of a freshness retaining agent 7 including an isothiocyanic acid ester containing carrier and a pouch for packaging the freshness retaining agent 7. The isothiocyanic acid ester adsorbing sealant layer 57 is provided on the inside of an arbitrary base material layer 52 and, in the sealant layer, either polypropylene or polyethylene resin is used and such a resin has such a shysical property a diffusion rate of at least 1.0×10 ^-3μm/min. COPYRIGHT: (C)1995,JPO
5	Preparation of ranitidine	JP23058993	1993-09-16	JPH06102656B2	1994-12-14	ジョン、フレデリック、シーガー; ロジャー、デンシー

6	Preparation of the amine derivative	JP13067385	1985-06-15	JPH0643382B2	1994-06-08	JIYON FUREDERITSUKU SHIIGAA; ROJIYAA DENSHII

7	Preparation of ranitidine	JP23058993	1993-09-16	JPH06211824A	1994-08-02	JIYON FUREDERITSUKU SHIIGAA; ROJIYAA DENSHII
PURPOSE: To prepare ranitidine from methyl isocyanate and nitromethane via an N-methyl-1-alkylthio-2-nitroetheneamine derivative. CONSTITUTION: Methyl isocyanate is reacted with carbanion of nitromethane (which is generated in situ by reaction of nitromethane and a corresponding base), by using dimethyl sulfoxide as a solvent, optionally in the presence of a cosolvent to obtain a compd. of formula I (Q is H, a cation derived from a suitable base or 1-4C alkyl). The compd. of formula I is subsequently reacted with a suitable alkylating agent to obtain a N-methyl-1-alkylthio-2- nitroetheneamine derivative of formula II (R ₁ is 1-4C alkyl), which is reacted further with 2-[5-(N,N-dimethyl-aminomethyl)-2-furanmethylthio]ethyl-amine to obtain ranitidine. COPYRIGHT: (C)1994,JPO
8	Raw miso package and production thereof	JP11728992	1992-05-11	JPH05310284A	1993-11-22	NAKAZAWA NORIO; SHIOKAWA SHUNICHI; HONMA JUNICHI; TOMITA TAKEHITO
PURPOSE: To prevent generation of carbon dioxide and pack raw MISO air-tight while retaining the flavor, by charging raw MISO mixed with aryl isothiocyancy or refined oil including the material in a packing container with a high gas barrier function and closely sealing it. CONSTITUTION: When raw MISO is packed, the raw MISO mixed with aryl isothiocyanate or refined oil including it is charged in a packing container having a high gas barrier function lower than 20cc/m ².atm.24hr in oxygen permeability and closely sealed. In this way, proliferation of yeast is restrained by aryl isothiocyanate and generation of carbon dioxide is prevented. And permeation of oxygen from the outside and also discoloration thereof are prevented since the MISO is sealed in the packing container having a high gas barrier function. Aryl isothiocyanate can be extracted as a refined oil from natural materials such as mustard or Japanese horseradish. The mixing ratio thereof to raw MISO is 0.01-1.0% by weight. COPYRIGHT: (C)1993,JPO&Japio
9	JPH0351699B2 -	JP33683787	1987-12-28	JPH0351699B2	1991-08-07	EMANYUERU ARESU; PATORITSUKU OOJU; ARUFURETSUDO MIRASUU; KUROODO RANDOTSUSHI

10	JPH01503713A -	JP50629988	1988-07-12	JPH01503713A	1989-12-14

11	JPH01502587A -	JP50315387	1987-05-18	JPH01502587A	1989-09-07

12	Manufacture of mercapto alcohol	JP33683787	1987-12-28	JPS63174965A	1988-07-19	EMANIYUERU ARESU; PATORITSUKU OOJIYU; ARUFURETSUDO MIRASUU; KUROODO RANDOUTSUSHI

13	Manufacture of amine derivative	JP13067385	1985-06-15	JPS6117557A	1986-01-25	JIYON FUREDERITSUKU SHIIGAA; ROJIYAA DENSHII

14	Aromatische Säuren	EP89810336.1	1989-05-01	EP0342157A2	1989-11-15	Chang, Jui Yoa, Dr.
Die Erfindung betrifft neue aromatische Säuren, insbesondere Verbindungen der Formel worin R₁ Niederalkyl darstellt, R₂ Niederalkyl ist, R₃ Wasserstoff, Carboxy oder Sulfo bedeutet, R₄ Carboxy oder Sulfo ist, G für eine gegebenenfalls substituierte 1,4-Phenylengruppe oder eine gegebenenfalls substituierte 1,4-Naphthylengruppe steht und worin entweder R₅ und R₆ gemeinsam für eine zusätzliche Bindung stehen und L ein Sauerstoff- oder ein Schwefelatom bedeutet oder worin R₅ Wasserstoff ist, R₆ Halogenmethyl bedeutet und L für ein Sauerstoffatom steht, und ihre Salze, die Verwendung der Verbindungen I und ihrer Salze, ein Verfahren zur Herstellung der Verbindungen I und ihrer Salze, in diesem Herstellungsverfahren verwendete Ausgangsstoffe und deren Salze, ein Verfahren zur Herstellung dieser Ausgangsstoffe und ihre Salze, eine Vorrichtung, in welcher die Verbindungen I und ihre Salze Verwendung finden, und ein Verfahren, in welchem diese Vorrichtung Verwendung findet. Die Verbindungen der Formel I können als Hilfsmittel bei der Untersuchung von Proteinen verwendet werden und sind in an sich bekannter Weise herstellbar.
15	Thiosulfinsäurederivate, und die Verwendung von Thiosulfinsäurederivaten zur Herstellung von Arzneimitteln für die Behandlung von Entzündungserkrankungen	EP88111119.9	1988-07-12	EP0299424A2	1989-01-18	Wagner, Hildebert, Prof.; Dorsch, Walter, Dr. med.
Die Erfindung betrifft Thiosulfinsäurederivate, Arzneimittel enthaltend diese Verbindungen und ihre Verwendung in der Medizin. Es wurde gefunden daß Thiosulfinsäurederivate ausgezeichnete entzündungshemmende Eigenschaften aufweisen. Insbesondere vorteilhaft erwiesen sich die Verbindungen in der Behandlung von PAF induzierten Entzündungsvorgängen des Brochialraumes.
16	N-ARYL-N'ALKYL SULFAMIDES AS MEK INHIBITORS	PCT/US2007066467	2007-04-11	WO2007121269A3	2008-12-24	YAN SHUNQI; VERNIER JEAN-MICHEL; HONG ZHI
This invention concerns N-(ortho phenylaminoaryl), N'-alkyl sulfamides which are inhibitors of MEK and are useful in the treatment of cancer and other hyperproliferative diseases.
17	COMPOSITIONS INCLUDING FLUORINATED PEROXIDES, METHODS OF MAKING, AND THE USE THEREOF	PCT/US0218082	2002-06-05	WO02098924A3	2003-08-28	KRASUTSKY PAVEL A; CARLSON ROBERT M; KOLOMITSYN IGOR V; WANG HONG
Methods of making compositions including fluorinated peroxides are disclosed. The compositions are useful, for example, for reacting with organic compounds. In one embodiment, novel peroxides are provided.
18	S-메틸 N-[{N-메틸-N-(N, N-이치환된 아미노설페닐)카바모일}옥시]티오아세트아미데이트 유도체의 제조방법	KR1019820000864	1982-02-26	KR100028086B1	1989-06-16	다게시고토-4

19	아민유도체의 제조방법	KR1019850004197	1985-06-14	KR1019860000255A	1986-01-27	로저댄세이; 죤프레데릭시거
내용 없음
20	FLUORINATION PROCESSES WITH ARYLSULFUR HALOTETRAFLUORIDES	PCT/US2009/036305	2009-03-06	WO2009114409A3	2009-09-17	UMEMOTO, Teruo; SINGH, Rajendra P.
New fluorination processes for introducing one or more fluorine atoms into target substrate compounds with arylsulfur halotetrafluorides are disclosed. Also disclosed are methods for preparation of arylsulfur trifluorides.

1 2 3 4 5 6 7 8 9 10

该功能需要专业版企业版VIP权限，您可以：