(E)-2,2-Dimethyl-3-pentenamide | 56930-53-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 羧酸及其衍生物
• 英文名称: (E)-2,2-Dimethyl-3-pentenamide
• 英文别名: trans-2,2-Dimethyl-3-pentensaeureamid；2,2-dimethyl-pent-3-enoic acid amide；2,2-Dimethyl-pent-3-ensaeure-amid；(E)-2,2-dimethylpent-3-enamide
• CAS: 56930-53-1
• 化学式: C₇H₁₃NO
• 分子量: 127.186
• InChiKey: STCQKDIKPYGUTO-SNAWJCMRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1
• 重原子数：
  9
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.57
• 拓扑面积：
  43.1
• 氢给体数：
  1
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  (E)-2,2-Dimethyl-3-pentenamide 在 sodium hypobromide 作用下， 生成 2-amino-2-methyl-trans-3-pentene
  参考文献：
  名称：

  Pivaloylnitrene. Reactions with olefins and dichloromethane solvent effect

  摘要：

  DOI：

  10.1021/jo00863a021
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 乙醚 、 氨 作用下， 生成 (E)-2,2-Dimethyl-3-pentenamide
  参考文献：
  名称：

  Courtot, Bulletin de la Societe Chimique de France, 1906, vol. <3> 35, p. 221

  摘要：

  DOI：

文献信息

• [EN] SUBSTITUTED OXADIAZOLES FOR COMBATING PHYTOPATHOGENIC FUNGI<br/>[FR] OXADIAZOLES SUBSTITUÉS POUR LUTTER CONTRE DES CHAMPIGNONS PHYTOPATHOGÈNES
  申请人：BASF SE

  公开号：WO2018114393A1

  公开（公告）日：2018-06-28

  The present invention relates to novel trifluoromethyloxadiazoles of the formula (I) or an N-oxide and/or their agriculturally useful salts and to their use for controlling phytopathogenic fungi, or to a method for combating phytopathogenic harmful fungi, which process comprises treating the fungi or the materials, plants, the soil or seeds to be protected against fungal attack, with an effective amount of at least one compound of the formula (I), or an N-oxide, or an agriculturally acceptable salt thereof; and to mixtures comprising at least one such compound and at least one further pesticidally active substance selected from the group consisting of herbicides, safeners, fungicides, insecticides, and plant growth regulators; and to agrochemical compositions comprising at least one compound of the formula I and to agrochemical compositions further comprising seeds.

  本发明涉及新型三氟甲氧二唑酮化合物的化学式(I)或其N-氧化物和/或其在农业中有用的盐，以及它们用于控制植物病原真菌的用途，或者用于对抗植物病原有害真菌的方法，该方法包括用化合物的有效量处理真菌或要受到真菌侵袭保护的材料、植物、土壤或种子，所述化合物为化学式(I)中的至少一种化合物，或N-氧化物，或其在农业中可接受的盐；以及包含至少一种此类化合物和至少一种来自除草剂、促生剂、杀菌剂、杀虫剂和植物生长调节剂组成的进一步具有杀虫活性的物质的混合物；以及包含至少一种化合物I的农药组合物，以及进一步包含种子的农药组合物。
• [EN] NOVEL AGROCHEMICAL COMPOSITION COMPRISING 4-SUBSTITUTED PHENYLAMIDINE COMPOUNDS<br/>[FR] NOUVELLE COMPOSITION AGROCHIMIQUE COMPRENANT DES COMPOSÉS DE PHÉNYLAMIDINE 4-SUBSTITUÉS
  申请人：PI INDUSTRIES LTD

  公开号：WO2021094906A1

  公开（公告）日：2021-05-20

  The present invention discloses a novel agrochemical composition comprising (1) at lease one compound of formula (I) wherein, R1, R2, R3, R4, R5, R6, R7 and m are as defined in the detailed description and (2) at least one further active ingredient. The present invention further discloses a method for controlling the phytopathogenic fungi of plants using the agrochemical composition according to invention.

  本发明公开了一种新型农药组合物，包括（1）至少一种具有式（I）的化合物，其中，R1、R2、R3、R4、R5、R6、R7和m如详细说明中所定义，以及（2）至少一种进一步的活性成分。本发明还公开了一种利用根据本发明的农药组合物控制植物病原真菌的方法。
• Stereocontrolled construction of condensed .gamma.-lactam ring systems by cationic cyclizations. Rearrangement of a .gamma.-lactam to a .delta.-lactam
  作者：Charles M. Marson、Urszula Grabowska、Timothy Walsgrove、Drake S. Eggleston、Paul W. Baures

  DOI：10.1021/jo00081a005

  日期：1994.1

  A new condensation of 3-alkenamides with benzaldehyde in acidic media, notably polyphosphoric acid, leads to gamma-lactam rings with high regio- and stereocontrol. One such gamma-lactam was shown to undergo a novel and stereocontrolled ring-expansion to a delta-lactam.
• SUBSTITUTED OXADIAZOLES FOR COMBATING PHYTOPATHOGENIC FUNGI
  申请人：BASF SE

  公开号：EP3555056A1

  公开（公告）日：2019-10-23
• NITROGEN-CONTAINING HETEROCYCLIC DERIVATIVE HAVING 11SS-HYDROXYSTEROID DEHYDROGENASE TYPE I INHIBITORY ACTIVITY
  申请人：Masuda Koji

  公开号：US20100240659A1

  公开（公告）日：2010-09-23

  Disclosed is a compound which is useful as an 11β-hydroxysteroid dehydrogenase type 1 inhibitor. A compound represented by the formula: , its pharmaceutically acceptable salt, or a solvate thereof, wherein Ring A is a group represented by the formula: Ring B is optionally substituted heteroaryl, provided that optionally substituted isoxazole is excluded, or optionally substituted heterocycle, R 1 is hydrogen or optionally substituted alkyl, R 2 is —OR 5 , —SR 5 , halogen, halogenated alkyl or the like, R 3 is optionally substituted alkyl or the like, R 4 is optionally substituted alkyl or the like, R 5 is optionally substituted alkyl or the like, R 6 is hydrogen or the like, R 7 and R 8 are each independently hydrogen or the like, R 10 and R 11 are each independently hydrogen or the like, R 12 is optionally substituted alkyl or the like, m and p are each independently integer of 1 to 3.