摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

methyl 5-deoxy-3-O-(2-fluorobenzyl)-5-C-methyl-2-0-(2-methylbenzyl)-D-xylofuranoside

中文名称
——
中文别名
——
英文名称
methyl 5-deoxy-3-O-(2-fluorobenzyl)-5-C-methyl-2-0-(2-methylbenzyl)-D-xylofuranoside
英文别名
methyl 5-deoxy-3-O-(2-fluorobenzyl)-5-C-methyl-2-O-(2-methylbenzyl)-D-xylofuranoside;(2R,3S,4R)-2-ethyl-3-[(2-fluorophenyl)methoxy]-5-methoxy-4-[(2-methylphenyl)methoxy]oxolane
methyl 5-deoxy-3-O-(2-fluorobenzyl)-5-C-methyl-2-0-(2-methylbenzyl)-D-xylofuranoside化学式
CAS
——
化学式
C22H27FO4
mdl
——
分子量
374.452
InChiKey
JWZXREKJTKHQTG-NJDFBWEVSA-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):
    4.1
  • 重原子数:
    27
  • 可旋转键数:
    8
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    36.9
  • 氢给体数:
    0
  • 氢受体数:
    5

反应信息

  • 作为产物:
    描述:
    methyl 5-deoxy-3-O-(2-fluorobenzyl)-5-C-methyl-D-xylofuranoside 、 2-甲基苄溴sodium hydroxide 作用下, 以 N-甲基乙酰胺 为溶剂, 生成 methyl 5-deoxy-3-O-(2-fluorobenzyl)-5-C-methyl-2-0-(2-methylbenzyl)-D-xylofuranoside
    参考文献:
    名称:
    Furobenzopyran derivatives, process for preparation of same and
    摘要:
    通式(I)的Furobenzopyran衍生物:##STR1##其中R.sup.1是较低的烷基,R.sup.2是较低的烷基,较低的烷氧基,卤素原子或被卤素原子取代的较低的烷基,R.sup.3是较低的烷基,较低的烷氧基,卤素原子,被卤素原子取代的较低的烷基,苯氧基或苄氧基,R.sup.4是氢原子或较低的烷基,m和n是0到4之间的任何整数,对杂草具有优异的除草活性,并对水稻、大豆和棉花等作物完全具有选择性。
    公开号:
    US05356866A1
点击查看最新优质反应信息

文献信息

  • Furobenzopyran derivatives, process for preparation of same and herbicides containing same as active components
    申请人:MITSUI TOATSU CHEMICALS, Inc.
    公开号:EP0572001A1
    公开(公告)日:1993-12-01
    Furobenzopyran derivatives of the general formula (I): in which R¹ is a lower alkyl group, R² is a lower alkyl group, lower alkoxy group, halogen atom or lower alkyl group substituted by a halogen atom, R³ is a lower alkyl group, lower alkoxy group, halogen atom, lower alkyl group substituted by a halogen atom, phenoxy group or benzyloxy group, R⁴ is a hydrogen atom or lower alkyl group and m and n are any integers between 0 and 4, have an excellent herbicidal activity on weeds and are completely selective to crops such as paddy rice, soybeans and cotton.
    通式(I)的呋喃并吡喃衍生物: 其中 R¹ 是低级烷基,R² 是低级烷基、低级烷氧基、卤素原子或被卤素原子取代的低级烷基,R³ 是低级烷基、低级烷氧基、卤素原子、被卤素原子取代的低级烷基、苯氧基或苄氧基,R⁴ 是氢原子或低级烷基,m 和 n 是 0 至 4 之间的任意整数,对杂草具有极佳的除草活性,对水稻、大豆和棉花等作物具有完全的选择性。
  • US5356866A
    申请人:——
    公开号:US5356866A
    公开(公告)日:1994-10-18
  • US5530146A
    申请人:——
    公开号:US5530146A
    公开(公告)日:1996-06-25
  • Furobenzopyran derivatives, process for preparation of same and
    申请人:Mitsui Toatsu Chemicals, Incorporated
    公开号:US05356866A1
    公开(公告)日:1994-10-18
    Furobenzopyran derivatives of the general formula (I): ##STR1## in which R.sup.1 is a lower alkyl group, R.sup.2 is a lower alkyl group, lower alkoxy group, halogen atom or lower alkyl group substituted by a halogen atom, R.sup.3 is a lower alkyl group, lower alkoxy group, halogen atom, lower alkyl group substituted by a halogen atom, phenoxy group or benzyloxy group, R.sup.4 is a hydrogen atom or lower alkyl group and m and n are any integers between 0 and 4, have an excellent herbicidal activity on weeds and are completely selective to crops such as paddy rice, soybeans and cotton.
    通式(I)的Furobenzopyran衍生物:##STR1##其中R.sup.1是较低的烷基,R.sup.2是较低的烷基,较低的烷氧基,卤素原子或被卤素原子取代的较低的烷基,R.sup.3是较低的烷基,较低的烷氧基,卤素原子,被卤素原子取代的较低的烷基,苯氧基或苄氧基,R.sup.4是氢原子或较低的烷基,m和n是0到4之间的任何整数,对杂草具有优异的除草活性,并对水稻、大豆和棉花等作物完全具有选择性。
查看更多