Naphthalenesulfonic acid, reaction products with formaldehyde and hydroxybenzenesulfonic acid | 93384-83-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: Naphthalenesulfonic acid, reaction products with formaldehyde and hydroxybenzenesulfonic acid
• 英文别名: formaldehyde;2-hydroxybenzenesulfonic acid;naphthalene-1-sulfonic acid
• CAS: 93384-83-9
• 化学式: C10H8O3S.C6H6O4S.CH2O
• 分子量: 412.4
• InChiKey: NTEKMGGXOFOJKG-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.54
• 重原子数：
  27
• 可旋转键数：
  2
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  163
• 氢给体数：
  3
• 氢受体数：
  8

文献信息

• Copper complexes of N-pyrazole, N-imidazole and N-triazole acetanilides, their preparation and their use as fungicides
  申请人：CIBA-GEIGY AG

  公开号：EP0000539A1

  公开（公告）日：1979-02-07

  Copper complexes of N-pyrazole-, N-imidazole- and N-triazole-acetanilide derivatives of formula: wherein R1 and R2 represent independently of each other methyl, ethyl, methoxy, ethoxy or halogen, R3 represents hydrogen, C1-C3-alkyl, C1-C4-alkoxy or halogen, R. represents hvdroaen or methvl R3 represents R4 represents 1,2-pyrazole, 1,3-imidazole, 1,2,4-triazole (1) or 1,2,4-triazole (4) A represents the anion of an organic or inorganic acid and n stands for the number 1 or 2 p stands for a number from 1 to 12 inclusive, their preparation and use as fungicides.

  式中 N-吡唑、N-咪唑和 N-三唑-乙酰苯胺衍生物的铜络合物： 其中 R1 和 R2 各自代表甲基、乙基、甲氧基、乙氧基或卤素、 R3 代表氢、C1-C3-烷基、C1-C4-烷氧基或卤素，R. 代表 hvdroaen 或 methvl R3 代表 R4 代表 1,2-吡唑、1,3-咪唑、1,2,4-三唑 (1) 或 1,2,4-三唑 (4) A 代表有机酸或无机酸的阴离子，以及 n 代表数字 1 或 2 p 代表从 1 到 12（含 12）的数字。
• Antimicrobial imidazole derivatives
  申请人：JANSSEN PHARMACEUTICA N.V.

  公开号：EP0061794A1

  公开（公告）日：1982-10-06

  A compound selected from the group consisting of an imidazole derivative having the formula the possible stereochemically isomeric forms, the acid addition salts and the metal salt complexes thereof, wherein: R, and R2 are, each independently, selected from the group consisting of hydrogen, halo and methyl; R3 and R4 are, each independently, selected from the group consisting of C1-C6-lower alkyl and C3-C4-lower alkenyl, or R3 and R4 form, together with the sulfur atoms to which they are attached and the bridging carbon atom, a 5-, 6- or 7-membered ring which is optionally substituted with 1 to 4 Cl-C4-lower alkyl groups; Rs is a member selected from the group consisting of hydrogen, C,-C4-lower alkyl, 2-propenyl and 2-propynyl; and n is 0, 1 or 2, antimicrobial compositions comprising at least one such compound as an active ingredient, a method of combating microorganisms by the use of such compounds and composition and a process of preparing the compounds of formula (I).

  一种选自以下组别的化合物：具有以下式子的咪唑衍生物 其可能的立体化学异构体、酸加成盐和金属盐络合物，其中 R 和 R2 各自独立地选自氢、卤素和甲基组成的组； R3 和 R4 各自独立地选自由 C1-C6 低级烷基和 C3-C4 低级烯基组成的组，或 R3 和 R4 与它们所连接的硫原子和桥接碳原子一起形成一个 5、6 或 7 元环，该环任选被 1 至 4 个 Cl-C4 低级烷基取代； Rs 选自氢、C,-C4-低级烷基、2-丙烯基和 2-丙炔基组成的组；以及 n 为 0、1 或 2，包含至少一种此类化合物作为活性成分的抗微生物组合物，通过使用此类化合物和组合物来抗击微生物的方法，以及制备式 (I) 化合物的工艺。
• Novel antimicrobial triazole derivatives
  申请人：JANSSEN PHARMACEUTICA N.V.

  公开号：EP0061798A2

  公开（公告）日：1982-10-06

  A compound selected from the group consisting of a 2'-amino-2'-phenyl-ethyl-1H-1,2,4-triazole of the formula (I) and the phytopharmaceutically acceptable salts and metal complexes thereof, wherein: R1 is a member selected from the group consisting of hydrogen, halo, C1-C4-alkyl, C1-C4- alkyloxy, and C1-C2-haloalkyl; R2 is a member selected from the group consisting of hydrogen, halo, Cl-C4-alkyl, C1-C4- alkyloxy, C1-C2-haloalkyl and phenyl; R3 is a member selected from the group consisting of hydrogen, C1-C12-alkyl, C3-C8- cycloalkyl which is optionally substituted with Cl-C4-alkyl, and aralkyl with maximum 2 carbon atoms in the alkyl part and optionally substituted on the phenyl nucleus with halo or nitro; R4 is a member selected from the group consisting of hydrogen and C1-C4-alkyl; whereby R3 and R4 may, together with the nitrogen atom to which they are attached, form a 3- to 7- membered saturated heterocyclic ring which may optionally be interrupted by oxygen, sulfur or NR5 and optionally substituted with R6, wherein R5 and R6 are each independently C1-C4-alkyl, a method of combating microorganisms by the use of such compounds, microbicidal agents comprising such compounds as active ingredients, processes of preparing the subject compounds and intermediates used therefore.

  选自由式（I）的 2'-氨基-2'-苯乙基-1H-1,2,4-三唑组成的组的化合物 及其植物药可接受的盐类和金属络合物，其中 R1 选自氢、卤代、C1-C4-烷基、C1-C4-烷氧基和 C1-C2 卤代烷基组成的组； R2 选自氢、卤代物、Cl-C4-烷基、C1-C4-烷氧基、C1-C2-卤代烷基和苯基组成的组； R3 选自氢、C1-C12-烷基、C3-C8-环烷基（可选择被 Cl-C4- 烷基取代）和芳烷基（烷基部分最多有 2 个碳原子，苯基核可选择被卤素或硝基取代）组成的组； R4 是选自氢和 C1-C4- 烷基的成员；其中 R3 和 R4 可与所连接的氮原子一起形成 3 至 7 个成员的饱和杂环，该杂环可任选被氧、硫或 NR5 中断，并任选被 R6 取代，其中 R5 和 R6 各自独立地为 C1-C4- 烷基。 使用此类化合物抗击微生物的方法、包含此类化合物作为活性成分的杀菌剂、制备相关化合物的工艺以及所用的中间体。
• Herbicidal compositions of acylated 1,3,5-tricarbonyl cyclohexane herbicides and antidotes therefor
  申请人：ICI AMERICAS INC.

  公开号：EP0298679A2

  公开（公告）日：1989-01-11

  A herbicidal composition characterised in that it comprises a herbicidally effective amount of an acylated 1,3,5-tricarbonyl cyclohexyl compound corresponding to the following general formula: and tautomeric enol forms thereof, which is optionally substituted in the cyclohexyl position, and R represents an optionally substituted aromatic moiety with one or more aromatic groups; and a non-phytotoxic antidotally effective amount of a compound selected from amides of haloalkanoic acids, N-phenylcarbamates, N-phenylsulfonyl carbamates and 1,8-naphthalic anhydride is disclosed, as is the production and use thereof.

  一种除草组合物，其特征在于它包含一种除草有效量的酰化 1,3,5-三羰基环己基化合物，其对应通式如下： 及其同分异构烯醇形式，该化合物在环己基位置被任选取代，且 R 代表带有一个或多个芳香基团的任选取代芳香基团；以及选自卤代烷酸酰胺、N-苯基氨基甲酸酯、N-苯基磺酰基氨基甲酸酯和 1,8-萘酸酐的非植物毒性有效量的化合物，并公开了其生产和使用方法。
• [EN] 1-PHENYL-2-PHENYLIMINOPYRROLIDINES AND THEIR USE AS HERBICIDES
  申请人：ICI AMERICAS INC.

  公开号：WO1990007498A1

  公开（公告）日：1990-07-12

  (EN) 1-Trifluoromethylphenyl-2-(substituted phenyl)iminopyrrolidines of formula (I), in which R is H, halogen, or C1-C4 alkyl; R' is CF3, CH3, CF2CHF2, OCF2CHF2, OCHF2, OCF3, SCH3, S(O)CH3, SO2CH3, methoxyiminomethyl, methoxyimino-1-ethyl, benzoyloxyiminomethyl, and benzoyloxyimino-1-ethyl; and X and Y are independently H, halogen, CN or CF3, are useful as herbicidal agents.(FR) Des 1-Trifluorométhylphényl-2-(phényl substitué)iminopyrrolidines de formule (I), dans laquelle R est H, halogène, ou alkyl C1-C4; R' est CF3, CH3, CF2CHF2, OCF2CHF2, OCHF2, OCF3, SCH3, S(O)CH3, SO2CH3, méthoxyiminométhyl, méthoxyimino-1-éthyl, benzoyloxyiminométhyl, et benzoyloxyimino-1-éthyl; et X et Y sont indépendamment H, halogène, CN ou CF3, sont utiles comme agents herbicides.

  该英文文本已翻译成中文如下： 单取代三氟甲基苯并杂环结构类药物（I）的衍生物，其中 R为 H、卤素或C1-C4-烷基；R' 为 CF3、CH3、CF2CHF2、OCF2CHF2、OCHF2、OCF3、 SCH3、S(O)CH3、SO2CH3、甲氧－双甲氨基甲基、甲氧－双甲基氨基、苯甲氧－双甲氨基甲基和苯甲氧－双甲基氨基；X和Y为独立的 H、卤素、CN或 CF3，具有除草效果。