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3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione | 110956-96-2

中文名称
——
中文别名
——
英文名称
3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione
英文别名
N-(2-fluoro-4-chloro-5-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione;3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropyliden-1,3-oxazolidine-2,4-dione;(2-Fluoro-4-chloro-5-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione;3-(4-chloro-2-fluoro-5-hydroxyphenyl)-5-propan-2-ylidene-1,3-oxazolidine-2,4-dione
3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione化学式
CAS
110956-96-2
化学式
C12H9ClFNO4
mdl
——
分子量
285.659
InChiKey
SFYRUKSKTPDKPR-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):
    3.1
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.17
  • 拓扑面积:
    66.8
  • 氢给体数:
    1
  • 氢受体数:
    5

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dionepalladium-carbon 作用下, 以 乙醇 为溶剂, 以89%的产率得到3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropyl-1,3-oxazolidine-2,4-dione
    参考文献:
    名称:
    Oxazolidinedione compounds, the process for preparing the same and
    摘要:
    该专利公开了一种以式(I)表示的噁唑啉二酮化合物:##STR1## 其中R.sup.1代表氢原子,具有1至5个碳原子的烷基,具有3至5个碳原子的环烷基,具有3至5个碳原子的烯基,具有3至5个碳原子的炔基或具有其烷基中1或2个碳原子的烷氧羰基基团;R.sup.2代表具有3至5个碳原子的烷基或具有3至5个碳原子的环烷基,X代表氯原子或氟原子;公开了制备该化合物的方法和以该噁唑啉二酮化合物为活性成分的除草剂组合物。上述噁唑啉二酮化合物对有用的作物具有高选择性,并对各种有害杂草具有强烈的除草活性。
    公开号:
    US05100457A1
  • 作为产物:
    描述:
    3-(2'-fluoro-4'-chloro-5'-methoxycarbonyloxyphenyl)-5-isopropyliden-1,3-oxazolidine-2,4-dionepotassium carbonate氯化铵乙醚 、 silica gel 作用下, 以 甲醇 为溶剂, 反应 2.0h, 以to give pure 3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione (1.60 g)的产率得到3-(2'-fluoro-4'-chloro-5'-hydroxyphenyl)-5-isopropylidene-1,3-oxazolidine-2,4-dione
    参考文献:
    名称:
    Oxazolidinedione derivatives, method of producing the derivatives, and
    摘要:
    本发明公开了一种新型噁唑烷二酮衍生物,其化学式如下:##STR1##(其中R.sup.1、R.sup.2、R.sup.3、R.sup.4和R.sup.5在规范中定义),以及一种制备该衍生物和含有该衍生物作为活性成分的除草剂的方法。本发明还公开了作为制备噁唑烷二酮衍生物的中间体的碳酸酯酯。这些新型衍生物对有害杂草具有优异的除草活性,对农作物的植物毒性低。
    公开号:
    US04983751A1
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文献信息

  • Methods of preparing fluorobenzene derivatives and related compounds
    申请人:Sagami Chemical Research Center
    公开号:US05391807A1
    公开(公告)日:1995-02-21
    Disclosed are fluorobenzene derivatives, which are important intermediates for producing herbicidal oxazolidinedione derivatives, and methods of producing them. The fluorobenzene derivatives include compounds of a formula (11): ##STR1## where X is a halogen atom, R.sup.3 is a nitro, amino or isocyanato group or R.sup.1 OCONH, and R.sup.1 is an alkyl or phenyl group. Via the intermediates of the invention, oxazolidinedione derivatives can be produced with high yield.
    本发明公开了氟苯生物及其制备方法。这些氟苯生物是生产除草剂噁唑烷二酮衍生物的重要中间体。所述氟苯生物包括公式(11)的化合物:##STR1## 其中X是卤素原子,R.sup.3是硝基、基或异氰酸基或R.sup.1 OCONH,而R.sup.1是烷基或苯基。通过本发明的中间体,可以高产地生产噁唑烷二酮衍生物
  • Bis(fluorophenyl) carbonate derivatives
    申请人:Sagami Chemical Research Center
    公开号:US05281742A1
    公开(公告)日:1994-01-25
    Disclosed are fluorobenzene derivatives, which are important intermediates for producing herbicidal oxazolidinedione derivatives, and methods of producing them. The fluorobenzene derivatives include compounds of a formula (11): ##STR1## where X is a halogen atom, R.sup.3 is a nitro, amino or isocyanato group or R.sup.1 OCONH, and R.sup.1 is an alkyl or phenyl group. Via the intermediates of the invention, oxazolidinedione derivatives can be produced with high yield.
    本发明涉及氟苯生物,它们是制备除草剂噁唑烷二酮衍生物的重要中间体,以及它们的制备方法。所述氟苯生物包括式(11)的化合物:##STR1## 其中X是卤素原子,R.sup.3是硝基,基或异氰酸基或R.sup.1 OCONH,R.sup.1是烷基或苯基。通过本发明的中间体,可以高产率地制备噁唑烷二酮衍生物
  • Fluorobenzene derivatives
    申请人:Sagami Chemical Research Center
    公开号:US05344953A1
    公开(公告)日:1994-09-06
    Disclosed are fluorobenzene derivatives, which are important intermediates for producing herbicidal oxazolidinedione derivatives, and methods of producing them. The fluorobenzene derivatives include compounds of a formula (11): ##STR1## where X is a halogen atom, R.sup.3 is a nitro, amino or isocyanato group or R.sup.1 OCONH, and R.sup.1 is an alkyl or phenyl group. Via the intermediates of the invention, oxazolidinedione derivatives can be produced with high yield.
    本发明公开了一种氟苯生物,其是制备除草剂噁唑烷二酮衍生物的重要中间体,并公开了制备它们的方法。所述氟苯生物包括式(11)的化合物:##STR1## 其中X为卤素原子,R.sup.3为硝基,基或异氰酸基或R.sup.1OCONH,R.sup.1为烷基或苯基。通过本发明的中间体,可以高产得到噁唑烷二酮衍生物
  • Oxazolidinedione compounds, the process for preparing the same and herbicidal composition containing the same
    申请人:SAGAMI CHEMICAL RESEARCH CENTER
    公开号:EP0382884A1
    公开(公告)日:1990-08-22
    An oxazolidinedione compound represented by the formula (I): wherein R1 represents a hydrogen atom, an alkyl group having 1 to 5 carbon atoms, a cycloalkyl group having 3 to 5 carbon atoms, an alkenyl group having 3 to 5 carbon atoms, an alkynyl group having 3 to 5 carbon atoms or an alkoxycarbonyl group having 1 or 2 carbon atoms in the alkyl moiety thereof, R2 represents an alkyl group having 3 to 5 carbon atoms or a cycloalkyl group having 3 to 5 carbon atoms, and X represents a chlorine atom or a fluorine atom; a process for preparing the same; and a herbicidal composition comprising the oxazolidinedione compound as an active component are disclosed. The above oxazolidinedione compounds exhibit a high selectivity for useful crop plants and a strong herbicidal activity with respect to various noxious weeds.
    一种由式(I)代表的噁唑烷二酮化合物: 其中 R1 代表氢原子、具有 1 至 5 个碳原子的烷基、具有 3 至 5 个碳原子的环烷基、具有 3 至 5 个碳原子的烯基、具有 3 至 5 个碳原子的炔基或在其烷基中具有 1 或 2 个碳原子的烷氧羰基,R2 代表具有 3 至 5 个碳原子的烷基或具有 3 至 5 个碳原子的环烷基,X 代表原子或原子;本发明公开了制备上述化合物的工艺;以及包含该噁唑烷二酮化合物作为活性成分的除草组合物。上述噁唑烷二酮化合物对有用的作物植物具有很高的选择性,对各种有害杂草具有很强的除草活性。
  • OXAZOLIDINEDIONE DERIVATIVES, PROCESS FOR THEIR PREPARATION, AND HERBICIDES CONTAINING THE SAME
    申请人:SAGAMI CHEMICAL RESEARCH CENTER
    公开号:EP0241559B1
    公开(公告)日:1991-10-30
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