1-Formyloxy-2-propyloxy-aethan | 20759-34-6

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: 1-Formyloxy-2-propyloxy-aethan
• 英文别名: formic acid-(2-propoxy-ethyl ester)；Ameisensaeure-(2-propoxy-aethylester)；2-Propoxyethyl formate
• CAS: 20759-34-6
• 化学式: C₆H₁₂O₃
• 分子量: 132.159
• InChiKey: SCWNVZTWXMKFJJ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  0.9
• 重原子数：
  9
• 可旋转键数：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  35.5
• 氢给体数：
  0
• 氢受体数：
  3

文献信息

• OPTICAL RECORDING MEDIUM AND COMPOUND USED FOR THE SAME
  申请人：SHIOZAKI Hiroyoshi

  公开号：US20090306376A1

  公开（公告）日：2009-12-10

  A compound comprising a ring structure including a ring composed of four carbon atoms and two nitrogen atoms and a substituted or unsubstituted amino group bonded to the ring structure.

  一种化合物，包括一个环结构，其中包括由四个碳原子和两个氮原子组成的环，以及与环结构相结合的取代或未取代的氨基团。
• Cationic amphiphilic 1,4-dihydropyridine derivatives useful for delivery of nucleotide containing compounds
  申请人：——

  公开号：US20030064954A1

  公开（公告）日：2003-04-03

  The present invention discloses amphiphilic 1,4-dihydropyridine derivatives useful for the preparation of a composition for delivering nucleotide containing compounds into a target cell and/or its nucleus. Said composition comprises 1,4-dihydropyridine derivatives having a good DNA condensing capacity and capability of self-association. Also disclosed are composition comprising said derivatives complexed with nucleotide containing compounds as well methods for the producing of said complexes. The invention is also related to the use of said 1,4-dihydropyridine derivatives for manufacturing systems for delivering nucleotide containing compounds useful in gene therapy and DNA vaccination.

  本发明揭示了两性的1,4-二氢吡啶衍生物，用于制备递送含核苷酸化合物至靶细胞和/或其细胞核的组合物。所述组合物包括具有良好DNA凝聚能力和自组装能力的1,4-二氢吡啶衍生物。还揭示了包含所述衍生物与含核苷酸化合物复合物的组合物以及制备所述复合物的方法。本发明还涉及使用所述1,4-二氢吡啶衍生物制造递送核苷酸含量化合物的系统，用于基因治疗和DNA疫苗。
• 2,3-Dihydro-6-nitroimidazo[2,1-b]oxazoles
  申请人：Tsubouchi Hidetsugu

  公开号：US20060094767A1

  公开（公告）日：2006-05-04

  The present invention provides a 2,3-dihydro-6-nitroimidazo[2,1-b]oxazole compound represented by the following general formula: wherein R 1 represents a hydrogen atom or C1-C6 alkyl group, n represents an integer of 0 to 6, R 2 represents a group —OR 3 or the like, and R 3 represents a hydrogen atom, C1-C6 alkyl group or the like, or R 1 and —(CH 2 ) n R 2 may bind to each other together with carbon atoms adjacent thereto through nitrogen atoms so as to form a spiro ring represented by the general formula (H): wherein R 41 is hydrogen, C1-C6 alkyl group or the like. The present compound has an excellent bactericidal action against Mycobacterium tuberculosis , multi-drug-resistant Mycobacterium tuberculosis , and atypical acid-fast bacteria.

  本发明提供了一种2,3-二氢-6-硝基咪唑并[2,1-b]噁唑化合物，其通式如下：其中，R1代表氢原子或C1-C6烷基，n代表0到6的整数，R2代表—OR3或类似的基团，R3代表氢原子、C1-C6烷基或类似的基团，或者R1和—(CH2)nR2可以通过相邻的碳原子通过氮原子结合在一起形成一个螺环，其通式为（H）：其中，R41为氢、C1-C6烷基或类似的基团。该化合物对结核分枝杆菌、多药耐药结核分枝杆菌和非典型酸性快速细菌具有优异的杀菌作用。
• Pyrazole derivatives as herbicides
  申请人：——

  公开号：US20020055639A1

  公开（公告）日：2002-05-09

  Compounds of formula I 1 R 11 is hydrogen, fluorine, chlorine, bromine or methyl; R 12 is hydrogen, halogen, methyl, halomethyl, nitro, amino, hydroxy, OHC—, HOC(O)—, cyano, C 1 -C 4 alkoxycarbonyl or halomethoxy; X 1 is O, S, R 20 N═ or R 25 ON═; R 13 is hydroxy, C 1 -C 6 alkoxy, C 3 -C 6 alkenyloxy, C 3 -C 6 alkynyloxy, C 1 -C 6 haloalkoxy, C 3 -C 6 -haloalkenyloxy, C 1 -C 6 alkoxy-C 1 -C 6 alkyl, C 3 -C 6 alkenyloxy-C 1 -C 6 alkyl, C 3 -C 6 alkynyloxy-C 1 -C 6 -alkyl, C 1 -C 6 alkoxy-C 1 -C 6 alkoxy-C 1 -C 6 alkyl, B 1 -C 1 -C 6 alkoxy, R 21 (R 22 )N, C 1 -C 6 alkyl, C 3 -C 6 -alkenyl, C 3 -C 6 alkynyl, C 2 -C 6 haloalkyl, C 3 -C 6 haloalkenyl, C 3 -C 6 cycloalkyl, C 3 -C 6 halocycloalkyl, B 1 -C 1 -C 6 alkyl, OHC—, C 1 -C 6 alkylcarbonyl, C 1 -C 6 alkylcarbonyloxy, C 1 -C 6 haloalkylcarbonyl, C 2 -C 6 alkenylcarbonyl, C 1 -C 6 alkoxycarbonyl, C 1 -C 6 alkyl-S(O) 2 —, C 1 -C 6 haloalkyl-S(O) 2 —, (C 1 -C 6 -alkyl) 2 N—N═CH—, 2 B 1 -CH═N—, (CH 3 ) 2 N—CH═N—, (C 1 -C 5 -hydroxyalkyl)-CH 2 —, (B 1 -C 1 -C 5 hydroxyalkyl)-CH 2 —, (B 1 -C 1 -C 5 haloalkyl)-CH 2 —, (hydroxy-C 1 -C 5 -alkyl)-O— or (B 1 -C 1 -C 5 hydroxyalkyl)-O—; or X 1 and R 13 together are a group ═N—Y— wherein Y is bonded to the ring nitrogen atom; and R 20 , R 21 , R 22 , R 25 , B 1 and y are as defined in claim 1, and the pyrazole N-oxides, agrochemically acceptable salts and stereoisomers of those compounds of formula I, have good selective herbicidal properties pre- and post-emergence. The preparation of those compounds and the use thereof as herbicidal active ingredients are described.

  式I的化合物中，R11为氢、氟、氯、溴或甲基；R12为氢、卤素、甲基、卤代甲基、硝基、氨基、羟基、OHC—、HOC(O)—、氰基、C1-C4烷氧羰基或卤代甲氧基；X1为O、S、R20N═或R25ON═;R13为羟基、C1-C6烷氧基、C3-C6烯基氧基、C3-C6炔基氧基、C1-C6卤代烷氧基、C3-C6卤代烯基氧基、C1-C6烷氧-C1-C6烷基、C3-C6烯基氧-C1-C6烷基、C3-C6炔基氧-C1-C6烷基、C1-C6烷氧-C1-C6烷氧-C1-C6烷基、B1-C1-C6烷氧基、R21(R22)N、C1-C6烷基、C3-C6烯基、C3-C6炔基、C2-C6卤代烷基、C3-C6卤代烯基、C3-C6环烷基、C3-C6卤代环烷基、B1-C1-C6烷基、OHC—、C1-C6烷基羰基、C1-C6烷基羰酸酯、C1-C6卤代烷基羰基、C2-C6烯基羰基、C1-C6烷氧羰基、C1-C6烷基-S(O)2—、C1-C6卤代烷基-S(O)2—、(C1-C6-烷基)2N—N═CH—、2B1-CH═N—、(CH3)2N—CH═N—、(C1-C5-羟基烷基)-CH2—、(B1-C1-C5羟基烷基)- —、(B1-C1-C5卤代烷基)- —、(羟基-C1-C5-烷基)-O—或(B1-C1-C5羟基烷基)-O—；或X1和R13一起是一个═N—Y—基团，其中Y与环氮原子相连；R20、R21、R22、R25、B1和y如权利要求1所定义，式I的吡唑烷氧化物、农药中可接受的盐和立体异构体具有良好的选择性除草性能，描述了这些化合物的制备和用作除草活性成分的用途。
• Novel herbicides
  申请人：——

  公开号：US20020156285A1

  公开（公告）日：2002-10-24

  Compounds of formula 1 1 R 1 is hydrogen, fluorine, chlorine, bromine or methyl; R 2 is C 1 -C 4 alkyl, C 1 -C 4 halogenalkyl, halogen, hydroxy, C 1 -C 4 alkoxy, C 1 -C 4 halogenalkoxy, nitro, amino or cyano; 2 R 3 , R 15 to R 39 and X 6 to X 19 are as defined in claim 1, and the agrochemically acceptable salts and stereoisomers of these compounds of formula I are suitable for use as herbicides.

  化合物的公式为11R1，其中R1是氢，氟，氯，溴或甲基；R2是C1-C4烷基，C1-C4卤代烷基，卤素，羟基，C1-C4烷氧基，C1-C4卤代烷氧基，硝基，氨基或氰基；2R3，R15到R39和X6到X19如权利要求1所定义，并且这些公式I的化合物的农药可接受盐和立体异构体适用于作为除草剂使用。