N,4-dimethylpentan-2-imine | 1290071-57-6

• 分子结构分类: 有机化合物 - 有机氮化合物
• 英文名称: N,4-dimethylpentan-2-imine
• CAS: 1290071-57-6
• 化学式: C₇H₁₅N
• 分子量: 113.203
• InChiKey: YEEWIWOCSCAWDX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  8
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.86
• 拓扑面积：
  12.4
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为产物：
  描述：

  4-甲基-2-戊酮 、 N-methyl-N-trimethylsilylcarbamic acid trimethylsilyl ester 在 三氟乙酸 作用下， 反应 8.0h， 生成 N,4-dimethylpentan-2-imine
  参考文献：
  名称：

  Alkyloximes and Imines via Silyl Carbamates

  摘要：

  [image omitted] The reactions between different N,O-bis-trimethylsilyl-carbamates and oxo compounds were studied. The N,O-bis-trimethylsilyl-N-methoxy-carbamate converts ketones to the corresponding O-methyl oximes. The product is usually a mixture of syn and anti isomers. If the carbonyl compound bears a hydroxyl group, the oxime formation and the O-silylation take place simultaneously. In the case of -haloketones, the undesired substitution of halogen was not observed. The reactions between N,O-bis-trimethylsilyl-N-methyl-carbamate and oxo compounds resulted in the corresponding imines, although the yield are moderate in some cases. Analoguos reaction of ferrocenylated oxo derivatives gave similar results.

  DOI：

  10.1080/00397911003707121

文献信息

• IMIDATE COMPOUND AND USE THEREOF FOR PEST CONTROL
  申请人：Kamiyama Hideo

  公开号：US20100210683A1

  公开（公告）日：2010-08-19

  There is provided a compound having an excellent controlling effect on arthropod pests represented by the formula (I-1): wherein Z represents an optionally substituted carbocyclic group or an optionally substituted heterocyclic group; G represents a -A 1 -R 1 group, etc.; X 0 represents a -A 2 -R 4 group, etc.; X represents a -A 2 -R 4 group, etc.; X 0 represents a -A 3 -R 6 group, etc.; or X and X 0 are optionally taken together to form a -A 2 -T 0 -A 3 - group; M 1 represents a —R 8 group, etc.; A 1 , A 2 and A 3 independently represent an oxygen atom, etc.; R 1 and R 8 independently represents an optionally substituted C1-C20 chain hydrocarbon group, etc.; R 4 and R 6 independently represent an optionally substituted C1-C6 chain hydrocarbon group, etc.; and T 0 represents an optionally substituted C2-C6 alkanediyl group.

  提供一种化合物，它对于以式(I-1)所代表的节肢动物害虫具有优异的控制效果：其中Z代表可选取代的碳环基团或可选取代的杂环基团；G代表-A1-R1基团等；X0代表-A2-R4基团等；X代表-A2-R4基团等；X0代表-A3-R6基团等；或X和X0可选地结合形成-A2-T0-A3-基团；M1代表-R8基团等；A1、A2和A3独立地代表氧原子等；R1和R8独立地代表可选取代的C1-C20链烃基团等；R4和R6独立地代表可选取代的C1-C6链烃基团等；而T0代表可选取代的C2-C6脂肪二基基团。
• US8318981B2
  申请人：——

  公开号：US8318981B2

  公开（公告）日：2012-11-27
• Alkyloximes and Imines via Silyl Carbamates
  作者：Ferenc Kardon、Mária Mörtl、Antal Csámpai、Kálmán Újszászy、Dezső Knausz

  DOI：10.1080/00397911003707121

  日期：2011.2.28

  [image omitted] The reactions between different N,O-bis-trimethylsilyl-carbamates and oxo compounds were studied. The N,O-bis-trimethylsilyl-N-methoxy-carbamate converts ketones to the corresponding O-methyl oximes. The product is usually a mixture of syn and anti isomers. If the carbonyl compound bears a hydroxyl group, the oxime formation and the O-silylation take place simultaneously. In the case of -haloketones, the undesired substitution of halogen was not observed. The reactions between N,O-bis-trimethylsilyl-N-methyl-carbamate and oxo compounds resulted in the corresponding imines, although the yield are moderate in some cases. Analoguos reaction of ferrocenylated oxo derivatives gave similar results.