cis-2-tert-Butyl-4-methyl-1,3-dioxolane | 26563-72-4

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 二氧戊环
• 英文名称: cis-2-tert-Butyl-4-methyl-1,3-dioxolane
• 英文别名: 2-tert-butyl-4-methyl-1,3-dioxolane
• CAS: 26563-72-4
• 化学式: C₈H₁₆O₂
• 分子量: 144.21
• InChiKey: HXZAHJCDQZCFMZ-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  10
• 可旋转键数：
  1
• 环数：
  1.0
• sp3杂化的碳原子比例：
  1.0
• 拓扑面积：
  18.5
• 氢给体数：
  0
• 氢受体数：
  2

文献信息

• Simple preparation method for dialkoxypropyl methylphosphonate
  申请人：JIANGSU GOOD HARVEST-WEIEN AGROCHEMICAL CO., LTD

  公开号：US10759818B2

  公开（公告）日：2020-09-01

  A simple preparation method for a dialkoxypropyl methylphosphonate, wherein a methyl halogenated phosphonate monoester is reacted with a 3,3-dialkoxypropyl magnesium or zinc halide to obtain a 3,3-dialkoxypropyl methylphosphonate. The starting materials are readily available, the operations are simple, the conditions are mild, the synthesis conversion rate is high, and the method is suitable for industrial production.

  一种简单的二烷氧基丙基甲基膦酸盐的制备方法，其中卤化膦酸甲酯单酯与 3,3-二烷氧基丙基卤化镁或卤化锌反应得到 3,3-二烷氧基丙基甲基膦酸盐。该方法起始原料易得，操作简单，条件温和，合成转化率高，适合工业化生产。
• THIADIAZOLE COMPOUND AND USE THEREOF
  申请人：Takyo Hayato

  公开号：US20100081693A1

  公开（公告）日：2010-04-01

  A thiadiazole compound represented by the formula (I): wherein R is a hydrogen atom, an optionally substituted C1-C7 chain hydrocarbon group etc., Z is an oxygen atom or a sulfur atom, X is a —NR 2 R 3 group etc., R 2 and R 3 each independently are a hydrogen atom, a C1-C4 alkyl group, a C3-C4 alkenyl group, a C1-C4 alkoxy group, or a phenyl group, or R 2 and R 3 bind to each other at the ends thereof to form a C2-C7 alkanediyl group, has excellent controlling effect on a noxious arthropod.
• SIMPLE PREPARATION METHOD FOR DIALKOXYPROPYL METHYLPHOSPHONATE
  申请人：JIANGSU GOOD HARVEST-WEIEN AGROCHEMICAL CO., LTD

  公开号：US20190284215A1

  公开（公告）日：2019-09-19

  A simple preparation method for a dialkoxypropyl methylphosphonate, wherein a methyl halogenated phosphonate monoester is reacted with a 3,3-dialkoxypropyl magnesium or zinc halide to obtain a 3,3-dialkoxypropyl methylphosphonate. The starting materials are readily available, the operations are simple, the conditions are mild, the synthesis conversion rate is high, and the method is suitable for industrial production.