1,1,3-tribromo-1-propene | 36417-14-8

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 1,1,3-tribromo-1-propene
• 英文别名: 1,1,3-tribromopropene；1,1,3-tribromo-propene；1,1,3-Tribrom-propen；1,1,3-Tribromoprop-1-ene
• CAS: 36417-14-8
• 化学式: C₃H₃Br₃
• 分子量: 278.769
• InChiKey: WIQIRUONTRQXRN-UHFFFAOYSA-N

物化性质

• 沸点：
  62-64 °C(Press: 0.5 Torr)
• 密度：
  2.4408 g/cm3

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  6
• 可旋转键数：
  1
• 环数：
  0.0
• 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：

  1,1,3-tribromo-1-propene 在 sodium carbonate 作用下， 生成 3,3-dibromo-2-propen-1-ol
  参考文献：
  名称：

  Allylic Chlorides. XXIV. 1,1,3-Trichloro-1-propene, 1,1-Dibromo-3-chloro-1-propene and Related Compounds^1,2

  摘要：

  DOI：

  10.1021/ja01569a028
• 作为产物：
  描述：

  1,1-二溴-1-丙烯 在 N-溴代丁二酰亚胺(NBS) 作用下， 生成 1,1,3-tribromo-1-propene
  参考文献：
  名称：

  Allylic Chlorides. XXIV. 1,1,3-Trichloro-1-propene, 1,1-Dibromo-3-chloro-1-propene and Related Compounds^1,2

  摘要：

  DOI：

  10.1021/ja01569a028

文献信息

• Dihalopropene compounds, insecticidal/acaricidal agents containing same,
  申请人：Sumitomo Chemical Company, Limited

  公开号：US05872137A1

  公开（公告）日：1999-02-16

  The dihalopropene compounds of the general formula \x9bI! have excellent insecticidal/acaricidal activity, so that they are satisfactorily effective for the control of noxious insects, mites and ticks.

  通用公式\x9bI!的二卤代丙烯化合物具有出色的杀虫/杀螨活性，因此它们对有害昆虫、螨和蜱的控制效果令人满意。
• The Synthesis of Stereodefined Trisubstituted Olefins From Olefin Templates Using Pd Catalysis - Synthesis of the Antihypertensive Isbogrel
  作者：Lawrence R. Rogers、Zissis Konstantinou、Madhav Reddy、Michael G. Organ

  DOI：10.1002/ejoc.201100849

  日期：2011.9

  A collection of highly functionalized, trisubstituted olefin building blocks (templates) have been developed for their Pd-catalyzed elaboration into more complex structures, including natural products and compounds of medicinal chemistry interest. The Pd-mediated transformations involve a combination of allylic substitution and cross-coupling reactions. The templates have been designed such that these

  已经开发了一系列高度官能化的三取代烯烃结构单元（模板），用于将它们在 Pd 催化下加工成更复杂的结构，包括天然产物和具有药物化学意义的化合物。Pd 介导的转化涉及烯丙基取代和交叉偶联反应的组合。模板的设计使得这些过程不仅具有高度的区域选择性和立体选择性，而且可以使用相同的催化剂在同一个烧瓶中依次进行转化。
• 3-aryluracils for the control of weeds
  申请人：Ciba-Geigy Corporation

  公开号：US05041156A1

  公开（公告）日：1991-08-20

  The present invention is concerned with heterocyclic compounds, namely 3-aryluracils of the general formula ##STR1## wherein R.sup.1, R.sup.2, R.sup.3, R.sup.4, R.sup.5 and Q are as described herein, as well as salts thereof and their manufacture, weed control compositions.

  本发明涉及杂环化合物，即一般式##STR1##中的3-芳基尿嘧啶，其中R.sup.1、R.sup.2、R.sup.3、R.sup.4、R.sup.5和Q如本文所述，以及其盐及其制备方法，除草剂组合物。
• Dihaloprene compound, insecticide/acaricide containing said
  申请人：Sumitomo Chemical Company, Limited

  公开号：US05530015A1

  公开（公告）日：1996-06-25

  There is disclosed a dihalopropene compound of the formula I: ##STR1## wherein l is an integer of 1 to 5; m is an integer of 1 to 4; R.sup.1 's and R.sup.2 's are the same or different and are independently halogen or various other groups; D is oxygen; X's are the same or different and are independently chlorine or bromine; Y is oxygen; Z, P and Q are the same or different and are independently nitrogen or CH, provided that P and Q are not simultaneously nitrogen, and when Y is sulfur, Z is CH. Also disclosed is an insecticide/acaricide comprising the dihalopropene compound as an active ingredient. The dihalopropene compound exhibits excellent insecticidal/acaricidal action. Further disclosed is an intermediate compound for use in the production of the dihalopropene compound.

  公开了一种具有以下结构的二卤代丙烯化合物：其中l为1到5的整数；m为1到4的整数；R^1和R^2相同或不同且独立地为卤素或其他各种基团；D为氧；X相同或不同且独立地为氯或溴；Y为氧；Z、P和Q相同或不同且独立地为氮或CH，但P和Q不能同时为氮，当Y为硫时，Z为CH。公开了一种含有上述二卤代丙烯化合物作为活性成分的杀虫剂/杀螨剂。该二卤代丙烯化合物表现出优异的杀虫/杀螨作用。还公开了用于生产上述二卤代丙烯化合物的中间体化合物。
• S-trifluorobutenyl derivatives and pesticidal uses thereof
  申请人：FMC Corporation

  公开号：US04748186A1

  公开（公告）日：1988-05-31

  S-trifluorobutenyl thiocarbonic acid esters of the formula ##STR1## and salts thereof, wherein X is R.sup.1 N or S and Y is RS or R.sup.3 R.sup.2 N; wherein R is a metal or a radical selected from alkyl, cycloalkylalkyl, halocycloalkylalkyl, alkenyl, haloalkyl, haloalkenyl, alkynyl, alkoxyalkyl, alkylthioalkyl, alkoxycarbonylalkyl, halophenoxyalkyl, trialkylsilylalkyl, (vinyl)dialkylsilylalkyl, (allyl)dialkylsilylalkyl, 2-chlorothiophene-5-ylmethyl, phenylalkyl, halophenylalkyl, nitrophenylalkyl, haloalkylphenylalkyl, dialkyl-2,3-dihydrobenzofuran-7-yl, [2-methyl-(1,1'-biphenyl)-3-yl]methyl, 3-phenoxybenzyl, phenylthioalkyl, halophenylthioalkyl, dialkylphosphoryl, dialkylthiophosphoryl, dialkylisoxazolylalkyl and thienylisoxazolylalkyl; wherein R.sup.1 is alkyl, cycloalkyl, cyano, dialkyl-2,3-dihydrobenzofuran-7-yl, halophenyl, halophenylalkyl, haloalkoxyphenyl, pyridinyl, halopyridinyl, alkyl-1,3,4-thiadiazolyl, haloalkyl-1,3,4-thiadiazolyl, benzothiazolyl, dialkyloxazolyl or thiazolinyl; wherein R.sup.2 is hydrogen or alkyl; and wherein R.sup.3 is alkyl, haloalkyl, cycloalkyl, cycloalkylalkyl, dialkylaminoalkyl, dialkyl-2-oxazolyl, 2-thiazolinyl, 2-benzothiazolyl, 4-phenyl-2-thiazolyl, alkyl-1,3,4-thiadiazolyl, haloalkyl-1,3,4-thiadiazolyl, pyridinyl, halopyridinyl, phenyl, halophenyl, halophenylalkyl, haloalkoxyphenyl, or dialkyl-2,3-dihydrobenzofuran-7-yl; provided that: when X is S, Y is R.sup.3 R.sup.2 N, when X is R.sup.1 N, Y is RS, R.sup.1 is other than alkyl and R is other than haloalkenyl; and when X is R.sup.1 N where R.sup.1 is CN and Y is RS, R is other than alkali metal. The compounds exhibit nematicidal and anthelmintic activity and are useful in agriculture and veterinary practice.

  化学式为##STR1##的S-三氟丁烯基硫代碳酸酯及其盐，其中X为R.sup.1 N或S，Y为RS或R.sup.3 R.sup.2 N；其中R为金属或从烷基、环烷基烷基、卤代环烷基烷基、烯基、卤代烷基、卤代烯基、炔基、烷氧基烷基、烷基硫基烷基、烷氧羰基烷基、卤代苯氧基烷基、三烷基硅烷基烷基、(乙烯基)二烷基硅烷基、(丙烯基)二烷基硅烷基、2-氯硫代吡啶-5-基甲基、苯基烷基、卤代苯基烷基、硝基苯基烷基、卤代烷基苯基烷基、二烷基-2,3-二氢苯并呋喃-7-基、[2-甲基-(1,1'-联苯)-3-基]甲基、3-苯氧基苄、苯硫基烷基、卤代苯硫基烷基、二烷基磷酰基、二烷基硫代磷酰基、二烷基异噁唑基烷基和噻唑基异噁唑基烷基；其中R.sup.1为烷基、环烷基、氰基、二烷基-2,3-二氢苯并呋喃-7-基、卤代苯基、卤代苯基烷基、卤代烷氧基苯基、吡啶基、卤代吡啶基、烷基-1,3,4-噻二唑基、卤代烷基-1,3,4-噻二唑基、苯并噻唑基、二烷氧唑基或噻唑啉基；其中R.sup.2为氢或烷基；其中R.sup.3为烷基、卤代烷基、环烷基、环烷基烷基、二烷基氨基烷基、二烷基-2-噁唑基、2-噻唑啉基、2-苯并噻唑基、4-苯基-2-噻唑基、烷基-1,3,4-噻二唑基、卤代烷基-1,3,4-噻二唑基、吡啶基、卤代吡啶基、苯基、卤代苯基、卤代苯基烷基、卤代烷氧基苯基或二烷基-2,3-二氢苯并呋喃-7-基；条件是：当X为S时，Y为R.sup.3 R.sup.2 N；当X为R.sup.1 N时，Y为RS，R.sup.1不是烷基且R不是卤代烯基；当X为R.sup.1 N且R.sup.1为CN时，Y为RS，R不是碱金属。这些化合物表现出线虫杀和驱虫活性，并在农业和兽医实践中有用。