ethylcycloheptyl ether | 53313-48-7

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: ethylcycloheptyl ether
• 英文别名: Ethoxycycloheptane
• CAS: 53313-48-7
• 化学式: C₉H₁₈O
• 分子量: 142.241
• InChiKey: YOTNQLMAZGVCRO-UHFFFAOYSA-N

物化性质

• 沸点：
  171-180 °C
• 密度：
  0.85±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.8
• 重原子数：
  10
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  9.2
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  溴代环庚烷 、 乙醇 在 potassium hydroxide 作用下， 反应 18.0h， 以62%的产率得到环庚烯
  参考文献：
  名称：

  Ammonium-Directed Oxidation of Cyclic Allylic and Homoallylic Amines

  摘要：

  The ammonium-directed olefinic oxidation of a range of cyclic allylic and homoallylic amines has been investigated. Functionalization of a range of allylic 3-(N,N-dibenzylamino)cycloalk-1-enes with m-CPBA in the presence of Cl3CCO2H gives exclusively the corresponding syn-epoxide for the 5-membered ring (> 99:1 dr), the anti-epoxide for the 8-membered ring (>99:1 dr), and predominantly the anti-epoxide for the 7-membered ring (94:6 dr). Oxidation of the homoallylic amines 3-(N-benzylamino)methylcyclohex-1-ene and 3-(N,N-dibenzylamino)methylcyclohex-1-ene gave, in both cases, the corresponding N-protected 1,2-anti-2,3-syn-3-aminomethylcyclohexane-1,2-diol with high levels of diastereoselectivity (>= 90:10 dr). The versatile synthetic intermediates resulting from these oxidation reactions are readily transformed into a range of amino diols.

  DOI：

  10.1021/jo9012783

文献信息

• 2-W-diaminocarboxylic acid compounds
  申请人：Rentzea Costin

  公开号：US20050085516A1

  公开（公告）日：2005-04-21

  2,ω-Diaminocarboxylic acid compounds of formula (I), where X, X 1 , Ar ω , Ar 2 and Y are as defined in claim 1, and their use as herbicides, are described.

  公式（I）中的2,ω-二氨基羧酸化合物，其中X，X1，Arω，Ar2和Y如权利要求1所定义，并描述了它们作为除草剂的用途。
• Substrate bound linker molecules for the construction of biomolecule microarrays
  申请人：International Business Machines Corporation

  公开号：US20040121399A1

  公开（公告）日：2004-06-24

  A series of photoactivatible surface bound linker molecules, which can be used to fabricate biomolecular arrays, is described. Specifically, a composition which includes a solid substrate; an organic linking group having one terminal end portion bound to the solid substrate and at least one other terminal end portion containing an alcohol or carbonyl functionality; and an acid labile protecting group selected from acetals and ketals bound to the alcohol or carbonyl functionality. A composition which comprises a solid substrate; an organic linking group having one terminal end portion bound to the solid substrate and at least one other terminal end portion containing an aldehyde group is also described. The present invention further provides a composition which includes a solid substrate; and at least one of a photoacid generator or a sensitizer bound to the solid substrate.

  本文描述了一系列光致活化表面结合连接分子，可用于制备生物分子阵列。具体来说，本发明涉及一种组合物，包括固体基质；有机连接基团，其具有一个端部与固体基质结合，至少一个其他端部含有醇或羰基功能基团；以及选择性地与醇或羰基功能基团结合的酸敏保护基团，所述酸敏保护基团选自缩醛和缩酮。本发明还提供了一种组合物，包括固体基质；有机连接基团，其具有一个端部与固体基质结合，至少一个其他端部含有醛基团。本发明还提供了一种组合物，包括固体基质；以及至少一种光酸发生剂或敏化剂，结合到固体基质上。
• FUNGICIDE HYDROXIMOYL-TETRAZOLE DERIVATIVES
  申请人：Beier Christian

  公开号：US20130012546A1

  公开（公告）日：2013-01-10

  The present invention relates to hydroximoyl-tetrazole derivatives of formula (I), their process of preparation, their use as fungicide active agents, particularly in the form of fungicide compositions and methods for the control of phytopathogenic fungi, notably of plants, using these compounds or compositions. wherein A represents a tetrazoyl group, Het represents a pyridyl group or a thiazolyl group and X represents various substituents.

  本发明涉及式（I）的羟肟基四唑衍生物，其制备方法，作为杀真菌活性剂的用途，特别是以杀真菌组合物的形式和使用这些化合物或组合物控制植物病原真菌，尤其是植物的方法。 其中，A代表四唑基团，Het代表吡啶基团或噻唑基团，X代表各种取代基。
• Photoresist composition
  申请人：Sumitomo Chemical Company, Limited

  公开号：EP0945764A2

  公开（公告）日：1999-09-29

  A photoresist composition which is particularly useful as a chemical amplification type photoresist is provided, wherein the photoresist composition contains a resin having a structural unit represented by the following formula (I) : wherein R1, R2 and R3 each independently represents a hydrogen atom or an alkyl group having 1 to 4 carbon atoms; R4 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms or an alkoxy group having 1 to 4 carbon atoms and R5 represents a hydrogen atom, alkyl group or aryl group, or R4 and R5 join together to form a ring, which may be heterocyclic; and R6 represents a hydrogen atom, an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms or a hydroxyl group.

  本发明提供了一种特别适用于化学放大型光刻胶的光刻胶组合物，其中该光刻胶组合物含有一种具有下式(I)所代表的结构单元的树脂： 其中 R1、R2 和 R3 各自独立地代表氢原子或具有 1 至 4 个碳原子的烷基；R4 代表氢原子、具有 1 至 4 个碳原子的烷基或具有 1 至 4 个碳原子的烷氧基，R5 代表氢原子、烷基或芳基，或 R4 和 R5 连接在一起形成环，该环可以是杂环；R6 代表氢原子、具有 1 至 4 个碳原子的烷基、具有 1 至 4 个碳原子的烷氧基或羟基。
• [DE] SUBSTITUIERTE AROMATISCHE PHOSPHONSÄUREDERIVATE<br/>[EN] SUBSTITUTED AROMATIC PHOSPHONIC ACID DERIVATIVES<br/>[FR] DERIVES AROMATIQUES SUBSTITUES D'ACIDE PHOSPHONIQUE
  申请人：BASF AKTIENGESELLSCHAFT

  公开号：WO1997030060A1

  公开（公告）日：1997-08-21

  (DE) Substituierte aromatische Phosphonsäurederivate der Formel (I) und deren Salze, wobei Eth = 1,2-Ethindiyl, geg. subst. Ethan- oder Ethen-1,2-diyl-Kette; y1 = O, S; y2, y3 = O, S oder -N(R6)-; R1, R2, R6, R7 = H, C1-C6-Alkyl, C1-C6-Halogenalkyl, Hydroxy-C1-C4-alkyl, Cyano-C1-C4-alkyl, C1-C4-Alkoxy-C1-C4-alkyl, C1-C4-Halogenalkoxy-C1-C4-alkyl, C3-C4-Alkenyloxy-C1-C4-alkyl, C3-C4-Alkinyloxy-C1-C4-alkyl, C3-C8-Cycloalkoxy-C1-C4-alkyl, Amino-C1-C4-alkyl, C1-C4-Alkylamino-C1-C4-alkyl, Di-(C1-C4-alkyl)amino--C1-C4-alkyl, C1-C4-Alkylthio-C1-C4-alkyl, C1-C4-Halogenalkylthio-C1-C4-alkyl, C3-C4-Alkenylthio-C1-C4-alkyl, C3-C4-Alkinylthio-C1-C4-alkyl, C1-C4-Alkylsulfinyl-C1-C4-alkyl, C1-C4-Halogenalkylsulfinyl-C1-C4-alkyl, C3-C4-Alkenylsulfinyl-C1-C4-alkyl, C3-C4-Alkinylsulfinyl-C1-C4-alkyl, C1-C4-Alkylsulfonyl-C1-C4-alkyl, C1-C4-Halogenalkylsulfonyl-C1-C4-alkyl, C3-C4-Alkenylsulfonyl-C1-C4-alkyl, C3-C4-Alkinylsulfonyl-C1-C4-alkyl, C3-C6-Alkenyl, C3-C6-Halogenalkenyl, Cyano-C3-C6-alkenyl, C3-C6-Alkinyl, C3-C6-Halogenalkinyl, Cyano-C3-C6-alkinyl, Hydroxycarbonyl-C1-C4-alkyl, (C1-C4-Alkoxy)-carbonyl-C1-C4-alkyl, (C1-C4-Alkylthio)carbonyl-C1-C4-alkyl, Aminocarbonyl-C1-C4-alkyl, (C1-C4-Alkyl)aminocarbonyl-C1-C4-alkyl, Di-(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, ggf. subst. C3-C8-Cycloalkyl, C3-C8-Cycloalkyl-C1-C4-alkyl, Phenyl oder Phenyl-C1-C4-alkyl oder geg. subst. 3- bis 7-gliedriges Heterocyclyl oder Heterocyclyl-C1-C4-alkyl, wobei alle Heterocyclen gewünschtenfalls ein Carbonyl- oder Thiocarbonyl-Ringglied enthalten können, oder R1 und R2 und/oder R1 und R6 und/oder R2 und R7 zusammen = ggf. subst. 1,2-Ethandiyl-, 1,3-Propylen-, Tetramethylen-, Pentamethylen- oder Ethylenoxyethylen-Kette, oder R1 und R2 zusammen = geg. subst. 1,2-Phenylen; R3 = CN, Halogen, C1-C4-Alkyl, C1-C4-Halogenalkyl, C1-C4-Alkoxy oder C1-C4-Halogenalkoxy; R4 = H, Halogen; R5 = bestimmter Heterocyclus. Verwendung: als Herbizide; zur Desikkation/Defoliation von Pflanzen.(EN) The invention concerns substituted aromatic phosphonic acid derivatives (I) and their salts, wherein: Eth = 1,2-ethinediyl, an optionally substituted ethane or ethene-1,2-diyl chain; y1 = O, S; y2, y3 = O, S or -N(R6)-; R1, R2, R6, R7 = H, C1-C6-alkyl, C1-C6 alkyl halide, hydroxy-C1-C4-alkyl, cyano-C1-C4-alkyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-alkoxy halide-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkinyloxy-C1-C4-alkyl, C3-C8-cycloalkoxy-C1-C4-alkyl, amino-C1-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, Di-(C1-C4-alkyl)amino-C1-C4-alkyl, C1-C4-alkylthio-C1-C4-alkyl, C1-C4-alkyl halide-thio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkinylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-C1-C4-alkyl, C1-C4-alkyl halide sulfinyl-C1-C4-alkyl, C3-C4-alkenylsulfinyl-C1-C4-alkyl, C3-C4-alkinylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, C1-C4-alkyl halide sulfonyl-C1-C4-alkyl, C3-C4-alkenylsulfonyl-C1-C4-alkyl, C3-C4-alkinylsulfonyl-C1-C4-alkyl, C3-C6-alkenyl, C3-C6-alkenyl halide, cyano-C3-C6-alkenyle, C3-C6-alkenyl halide, cyano-C3-C6-alkenyl, C3-C6-alkinyl, C3-C6-alkinyl halide, cyano-C3-C6-alkinyl, hydroxycarbonyl-C1-C4-alkyl, (C1-C4-alkoxy)-carbonyl-C1-C4-alkyl, (C1-C4-alkylthio)carbonyl-C1-C4alkyl, aminocarbonyl-C1-C4-alkyl, (C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, Di-(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, C3-C8-cycloalkyl, C3-C8-cycloalkyl-C1-C4-alkyl, phenyl ou phenyl-C1-C4-alkyl optionally substituted 3- to 7-member heterocyclyl or heterocyclyl-C1-C4 alkyl, wherein all the heterocyclenes can optionally contain a carbonyl- or thiocarbonyl ring member; or R1 and R2 and/or R1 and R6 and/or R2 and R7 together are an optionally substituted 1,2-ethanediyl-, 1,3-propylene-, tetramethylene-, pentamethylene or ethyleneoxyethylene chain; or R1 and R2 together are an optionally substituted 1,2-phenylene; R3 = CN, halogen, C1-C4 alkyl, C1-C4 alkyl halide, C1-C4 alkoxy or C1-C4 alkoxy halide; R4 = H, halogen; and R5 = a given heterocyclic ring. The invention further concerns the use of these substances as herbicides and for the desiccation/defoliation of plants.(FR) L'invention concerne des dérivés aromatiques substitués d'acide phosphonique de la formule (I) et leurs sels, formule dans laquelle Eth désigne 1,2-éthindiyle, une chaîne éthane- ou éthène-1,2-diyle éventuellement substituée; y1 désigne O, S; y2, y3 désignent O, S ou -N(R6)-; R1, R2, R6, R7 désignent H, alkyle C1-C6, halogénure d'alkyle C1-C6, hydroxy-alkyle C1-C4, cyano-alkyle C1-C4, alcoxy C1-C4-alkyle C1-C4, halogénure d'alcoxy C1-C4-alkyle C1-C4, alcényloxy C3-C4-alkyle C1-C4, alcynyloxy C3-C4-alkyle C1-C4, cycloalcoxy C3-C8-alkyle C1-C4, amino-alkyle C1-C4, alkylamino C1-C4-alkyle C1-C4, di-(alkyle C1-C4)amino-alkyle C1-C4, alkylthio C1-C4-alkyle C1-C4, halogénure d'alkylthio C1-C4-alkyle C1-C4, alkénylthio C3-C4-alkyle C1-C4, alcynylthio C3-C4-alkyle C1-C4, alkylsulfinyle C1-C4-alkyle C1-C4, halogénure d'alkylsulfinyle C1-C4-alkyle C1-C4, alcénylsulfinyle C3-C4-alkyle C1-C4, alcynylsulfinyle C3-C4-alkyle C1-C4, alkylsulfonyle C1-C4-alkyle C1-C4, halogénure d'alkylsulfonyle C1-C4-alkyle C1-C4, alcénylsulfonyle C3-C4-alkyle C1-C4, alcényle C3-C6, halogénure d'alcényle C3-C6, cyano-alcényle C3-C6, alcynyle C3-C6, halogénure d'alcynyle C3-C6, cyano-alcynyle C3-C6, hydroxycarbonyle-alkyle C1-C4, (alcoxy C1-C4)-carbonyle-alkyle C1-C4, (alkylthio C1-C4)carbonyle-alkyle C1-C4, aminocarbonyle-alkyle C1-C4, (alkyle C1-C4)aminocarbonyle-alkyle C1-C4, di-(alkyle C1-C4)aminocarbonyle-alkyle C1-C4, di-(alkyle C1-C4)aminocarbonyle-alkyle C1-C4, cycloalkyle C3-C8 évent. subst., cycloalkyle C3-C8-alkyle C1-C4, phényle ou phényle-alkyle C1-C4 ou hétérocyclyle évent. subst. ayant entre 3 et 7 chaînons ou hétérocyclyle-alkyle C1-C4, tous les hétérocycles pouvant éventuellement contenir un chaînon cyclique carbonyle ou thiocarbonyle, ou R1 et R2 et/ou R1 et R6 et/ou R2 et R7 désignent conjointement une chaîne 1,2-éthandiyle, 1,3-propylène, tétraméthylène, pentaméthylène ou éthylènoxyéthylène évent. subst., ou R1 et R2 désignent conjointement 1,2-phénylène évent. subst.; R3 désigne CN, halogène, alkyle C1-C4, halogénure d'alkyle C1-C4, alcoxy C1-C4 ou halogénure d'alcoxy C1-C4; R4 désigne H, halogène; R5 désigne un hétérocycle déterminé. Ces dérivés s'utilisent comme herbicides et dans la dessiccation/défoliation de plantes.

  (DE) Substituierte aromatische Phosphonsäurederivate der Formel (I) und deren Salze, wobei Eth = 1,2-Ethindiyl, gegebenenfalls substituierte Ethan- oder Ethen-1,2-diyl-Kette; y1 = O, S; y2, y3 = O, S oder -N(R6)-; R1, R2, R6, R7 = H, C1-C6-alkyl, C1-C6-Halogenalkyl, Hydroxy-C1-C4-alkyl, Cyano-C1-C4-alkyl, C1-C4-Alkoxy-C1-C4-alkyl, C1-C4-Alkylhalogen-C1-C4-alkyl, C3-C4-Alkenyloxy-C1-C4-alkyl, C3-C4-Alkinyloxy-C1-C4-alkyl, C3-C8-Cycloalkoxy-C1-C4-alkyl, Aminooxy-C1-C4-alkyl, C1-C4-Alkylaminooxy-C1-C4-alkyl, Di-(C1-C4-alkyl)aminooxy-C1-C4-alkyl, C1-C4-Alkylthio-C1-C4-alkyl, C1-C4-Alkylhalogen-C1-C4-alkylthio, C3-C4-Alkenylthio-C1-C4-alkyl, C3-C4-Alkinyelthio-C1-C4-alkyl, C1-C4-Alkylsulfinyl-C1-C4-alkyl, C1-C4-Alkylhalogen-C1-C4-sulfinyl, C3-C4-Alkenylsulfinyl-C1-C4-alkyl, C3-C4-Alkinyel sulfinyl-C1-C4-alkyl, C1-C4-Alkylsulfonyl-C1-C4-alkyl, C1-C4-Alkylhalogen-C1-C4-sulfonyl, C3-C4-Alkenylsulfonyl-C1-C4-alkyl, C3-C4-Alkinyel sulfonyl-C1-C4-alkyl, C3-C6-Alkenyl, C3-C6-Halogenalkenyl, Cyanocarbonyl-C3-C6-alkyl, C3-C6-Halogenalkenyl, Cyanocarbonyl-C3-C6-alkyl, C3-C6-Alkinyel, C3-C6-Halogenalkinyel, Cyanocarbonyl-C3-C6-alkyl, C3-C6-Alkynyl, C3-C6-Halogenalkynyl, Cyanocarbonyl-C3-C6-alkyl, C3-C6-Alkylsulfonyl, C3-C6-Halogenalksulfonyl-C3-C6-alkyl, C3-C6-Alkenylsulfonyl, C3-C6-Alkinyel sulyonyl-C3-C6-alkyl, C3-C8-Cycloalkyl, C3-C8-Cycloalkyl-C1-C4-alkyl, Phényle ou Phényle-C1-C4-alkyl, substituonymatches_optional 3-à 7-gliedriges Heterocyclyl ou Heterocyclany-C1-C4-alkyl, où tous les Heterocyclyl peuvent être optionnellement conténs unMEMBRE RING Carroll ou thiocarbonyl-; ou R1 et R2 et/ou R1 et R6 et/ou R2 et R7 ensemble sont un optionnellement substitué 1,2-ethanediyl-, 1,3-propylene-, tétraéthylé-, pentaméthylène Ou éthylènoxyéthylène, ou R1 et R2 ensemble sont optionnellement substitué 1,2-Phényne; R3 = CN, Halogen, C1-C4-alkyl, C1-C4-Halogenalkyl, C1-C4-Alkoxy ou C1-C4-Alkoxihalogen; R4 = H, Halogen; et R5 = un Heterocycles donné. L'invention s'utilise comme des herbicides et pour le déso Vicariat de la séchage / décolture des plantes.