1-氯-2,3,5-三甲基苯 | 31053-98-2

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 1-氯-2,3,5-三甲基苯
• 英文名称: 1-chloro-2,3,5-trimethyl-benzene
• 英文别名: 1-Chlor-2,3,5-trimethyl-benzol；1-Chloro-2,3,5-trimethylbenzene
• CAS: 31053-98-2
• 化学式: C₉H₁₁Cl
• 分子量: 154.639
• InChiKey: YDAYZEFHKUCVII-UHFFFAOYSA-N

物化性质

• 沸点：
  215.0±9.0 °C(Predicted)
• 密度：
  1.029±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.6
• 重原子数：
  10
• 可旋转键数：
  0
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.33
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

反应信息

• 作为反应物：
  描述：

  1-氯-2,3,5-三甲基苯 、 硝酸 生成 alkaline earth salt of/the/ methylsulfuric acid
  参考文献：
  名称：

  Huender, Recueil des Travaux Chimiques des Pays-Bas, 1915, vol. 34, p. 21

  摘要：

  DOI：
• 作为产物：
  描述：

  alkaline earth salt of/the/ methylsulfuric acid 在 copper(l) chloride 作用下， 生成 1-氯-2,3,5-三甲基苯
  参考文献：
  名称：

  Huender, Recueil des Travaux Chimiques des Pays-Bas, 1915, vol. 34, p. 21

  摘要：

  DOI：

文献信息

• PYRAZOLOPYRIMIDINE DERIVATIVE
  申请人：Mitsubishi Tanabe Pharma Corporation

  公开号：EP1903045A1

  公开（公告）日：2008-03-26

  A pyrazolopyrimidine derivative of the formula [I] wherein R1 is an optionally substituted aromatic ring group, an optionally substituted lower alkyl group or an optionally substituted amino group; R2 is an optionally substituted aromatic ring group; R3 is an optionally substituted lower alkyl group; and R4 is a hydrogen atom, a lower alkyl group, a halogen atom, a nitro group or an amino group; or a pharmaceutically acceptable salt thereof is useful as an antagonist of CRF receptor.

  公式[I]中的吡唑吡嘧啶衍生物，其中R1是可选择取代的芳香环基团、可选择取代的较低烷基基团或可选择取代的氨基团；R2是可选择取代的芳香环基团；R3是可选择取代的较低烷基基团；R4是氢原子、较低烷基基团、卤素原子、硝基基团或氨基团；或其药用可接受盐可用作CRF受体拮抗剂。
• Pyrazolopyrimidine Derivative
  申请人：Kashiwagi Toshihiko

  公开号：US20090234117A1

  公开（公告）日：2009-09-17

  A pyrazolopyrimidine derivative of the formula [I] wherein R 1 is an optionally substituted aromatic ring group, an optionally substituted lower alkyl group or an optionally substituted amino group; R 2 is an optionally substituted aromatic ring group; R 3 is an optionally substituted lower alkyl group; and R 4 is a hydrogen atom, a lower alkyl group, a halogen atom, a nitro group or an amino group; or a pharmaceutically acceptable salt thereof is useful as an antagonist of CRF receptor.

  公式[I]中的吡唑吡嗪衍生物，其中R1是可选取代的芳香环基团、可选取代的较低烷基团或可选取代的氨基团；R2是可选取代的芳香环基团；R3是可选取代的较低烷基团；R4是氢原子、较低烷基团、卤原子、硝基或氨基团；或其药学上可接受的盐，可用作CRF受体拮抗剂。
• Azoline Compounds for Combating Arthropod Pests
  申请人：Koradin Christopher

  公开号：US20100010058A1

  公开（公告）日：2010-01-14

  The present invention relates to azoline compounds and their salts which are useful for combating arthropod pests. The present invention also relates to a method for combating arthropod pests and to agricultural compositions for combating said pests. It has been found that these objectives can be achieved by azoline compounds of the general formulae Ia or Ib, wherein X is S, O or NR 4 ; Ar is phenyl or a 5 or 6 membered heteroaromatic ring; R 1 is H, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, phenyl, a heteroaromatic ring etc.; R 2a , R 2b are H, CN, C 1 -C 6 -alkyl etc.; R 1 together with R 2a may also form a linear C 2 -C 4 -alkandiyl; R 3a-d are H, halogen, C 1 -C 6 -alkyl etc.

  本发明涉及用于对抗节肢动物害虫的噁唑啉化合物及其盐。本发明还涉及一种对抗节肢动物害虫的方法和用于对抗上述害虫的农业组合物。已经发现，通过通式Ia或Ib的噁唑啉化合物可以实现这些目标，其中X为S、O或NR4；Ar为苯基或5或6成员杂芳环；R1为H、C1-C6烷基、C2-C6烯基、苯基、杂芳环等；R2a、R2b为H、CN、C1-C6烷基等；R1与R2a还可以形成线性C2-C4烷二基；R3a-d为H、卤素、C1-C6烷基等。
• Pesticidal Compositions
  申请人：Kordes Markus

  公开号：US20080312085A1

  公开（公告）日：2008-12-18

  The present invention relates to 1-(Azolin-2-yl)-amino-alkane compounds, which are useful for combating insects, arachnids and nematodes. The present invention also relates to a method for combating animal pests selected from insects, arachnids and nematodes, and to agricultural compositions for combating animal pests. It has been found that animal pests can be combated by 1-(Azolin-2-yl)-amino-alkane compounds of the general formula I: wherein A is a radical of the formulae A 1 or A 2 : and wherein X is sulfur or oxygen and W, B and R 1 to R 6 are defined as in the description.

  本发明涉及1-(Azolin-2-yl)-amino-烷基化合物，其可用于对抗昆虫、蜘蛛和线虫。本发明还涉及一种用于对抗昆虫、蜘蛛和线虫等动物害虫的方法，以及用于对抗动物害虫的农业组合物。发现可以通过通式I中的1-(Azolin-2-yl)-amino-烷基化合物对动物害虫进行对抗，其中A是式A1或A2的基团：X是硫或氧，W、B和R1至R6如描述中所定义。
• Olefin polymerization catalyst system useful for polar monomers
  申请人：Baugh Sauders Lisa

  公开号：US20070197751A1

  公开（公告）日：2007-08-23

  This invention relates to copolymers produced by a polymerization method comprising contacting at least one olefin monomer, at least one polar monomer, an optional activator, and a catalyst compound represented by the formula: wherein M is selected from groups 3-11 of the periodic table; L 1 represents a formal anionic ligand, L 2 represents a formal neutral ligand, a is an integer greater than or equal to 1; b is greater than or equal to 0; c is greater than or equal to 1, E is nitrogen or phosphorus, Ar 0 is arene, R 1 -R 4 are, each independently, selected from hydrogen, hydrocarbyl, substituted hydrocarbyl or functional group, provided however that R 3 and R 4 do not form a naphthyl ring, N is nitrogen and O is oxygen.

  本发明涉及通过聚合方法制备的共聚物，该方法包括接触至少一种烯烃单体、至少一种极性单体、可选的活化剂和催化剂化合物。该催化剂化合物的化学式为：其中M从周期表的3-11组中选择；L1表示正离子配体，L2表示中性配体，a是大于等于1的整数；b大于等于0；c大于等于1；E是氮或磷，Ar0是芳烃，R1-R4分别选择自氢、烃基、取代烃基或功能基，但R3和R4不形成萘环，N是氮，O是氧。