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2-carbamoyl-cyclohex-1-enecarboxylic acid | 81951-65-7

中文名称
——
中文别名
——
英文名称
2-carbamoyl-cyclohex-1-enecarboxylic acid
英文别名
2-Carbamoyl-cyclohex-1-encarbonsaeure;2-Carbamoyl-1-cyclohexene-1-carboxylic acid;2-carbamoylcyclohexene-1-carboxylic acid
2-carbamoyl-cyclohex-1-enecarboxylic acid化学式
CAS
81951-65-7
化学式
C8H11NO3
mdl
——
分子量
169.18
InChiKey
VWFXHFHEOSNVQR-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    12
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    80.4
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 ammonium hydroxide 作用下, 生成 2-carbamoyl-cyclohex-1-enecarboxylic acid
    参考文献:
    名称:
    Kuester, Hoppe-Seyler's Zeitschrift fur Physiologische Chemie, 1908, vol. 55, p. 519,520, 522
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • TETRAHYDROPHTHALAMIDE DERIVATIVE, INTERMEDIATE FOR PRODUCING THE SAME, PRODUCTION OF BOTH, AND HERBICIDE CONTAINING THE SAME AS ACTIVE INGREDIENT
    申请人:SAGAMI CHEMICAL RESEARCH CENTER
    公开号:EP0635485A1
    公开(公告)日:1995-01-25
    A 3,4,5,6-tetrahydrophthalamide derivative and a 3,4,5,6-tetrahydroisophthalimide derivative, both having an excellent efficay as the active ingredient of a herbicide, and an industrial process for efficiently producing these higher-performance, herbicidally active compounds. A tetrahydrophthalamide derivative represented by general formula (I) is produced by the reaction of a tetrahydrophthalimide derivative, prepared by the reaction of a halogenated 5-cycloalkyloxyaniline derivative with 3,4,5,6-tetrahydrophthalic anhydride, or of the tetrahydroisophthalimide derivative of the invention with various amines. These tetrahydrophthalamide and tetrahydroisophthalimide derivatives have an excellent herbicidal effect in the treatment of lowland and upland soils and foliage treatment. The tetrahydroisophthalimide derivative is useful also as an intermediate for producing the tetrahydrophthalamide derivative and the like.
    一种3,4,5,6-四氢邻苯二甲酰胺衍生物和一种3,4,5,6-四氢异邻苯二甲酰亚胺生物,这两种衍生物作为除草剂的活性成分具有极佳的功效,以及一种高效生产这些性能更佳、除草活性更强的化合物的工业工艺。通过卤化 5-环烷氧基苯胺生物3,4,5,6-四氢邻苯二甲酸酐反应制备的四氢邻苯二甲酰亚胺生物,或本发明的四氢异邻苯二甲酰亚胺生物与各种胺反应制备通式 (I) 所代表的四氢邻苯二甲酰亚胺生物。这些四氢邻苯二甲酰胺和四氢异邻苯二甲酰亚胺生物在处理低地和高地土壤和叶片方面具有极佳的除草效果。四氢异邻苯二甲酰亚胺生物还可用作生产四氢邻苯二甲酰胺衍生物等的中间体。
  • Solid-phase affinity-based method for preparing and manipulating an analyte-containing solution
    申请人:Stolowitz Mark L.
    公开号:US20090215192A1
    公开(公告)日:2009-08-27
    A method for preparing an analyte-containing solution, which is compatible with surface-tension-directed liquid droplet manipulation and solid-phase affinity-based assays, is disclosed. The method comprises providing an affinity capture surface comprising a substrate surface having a plurality of first and second surface modifiers associated therewith, wherein the first and second surface modifiers render the affinity capture surface wettable and resistant to non-specific protein adsorption, and wherein the second surface modifiers are capable of selectively retaining an analyte, contacting the affinity capture surface with the analyte to form analyte/surface modifier complexes between the analyte and the second surface modifiers, and cleaving the first and second surface modifiers to release terminal portions of the first and second surface modifiers and the analyte into a solution in contact with the affinity capture surface, thereby yielding the analyte-containing solution and generating a hydrophobic surface. Novel affinity capture surfaces and methods for preparing the same are also disclosed.
  • US5385925A
    申请人:——
    公开号:US5385925A
    公开(公告)日:1995-01-31
  • US5506190A
    申请人:——
    公开号:US5506190A
    公开(公告)日:1996-04-09
  • US5554581A
    申请人:——
    公开号:US5554581A
    公开(公告)日:1996-09-10
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