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2,3,3-三氯丙-2-烯醛 | 3787-28-8

中文名称
2,3,3-三氯丙-2-烯醛
中文别名
——
英文名称
trichloro-acrylaldehyde
英文别名
trichloroacrolein;trichloropropenal;Trichlor-acrylaldehyd;Trichloracrolein;2,3,3-Trichloropropenal;2,3,3-trichloroprop-2-enal
2,3,3-三氯丙-2-烯醛化学式
CAS
3787-28-8
化学式
C3HCl3O
mdl
MFCD00154308
分子量
159.399
InChiKey
ZLWJEEVJKLGSRT-UHFFFAOYSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

物化性质

  • 沸点:
    222.6°C (rough estimate)
  • 密度:
    1.7293 (rough estimate)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    7
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 海关编码:
    2913000090

SDS

SDS:fc8a9d634031ff4d9ba31f9d36bc1543
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Chemistry of Polyhalogenated Nitrobutadienes, 2: Synthesis of <i>N</i>-Tetrachloro­allylidene-<i>N</i>′-arylhydrazines by a Formal Synproportionation Reaction
    作者:Dieter Kaufmann、Viktor Zapol’skii、Eva Nutz、Jan Namyslo、Arnold Adam
    DOI:10.1055/s-2006-950187
    日期:2006.9
    The reaction of 2-nitropentachlorobuta-1,3-diene with a variety of anilines substituted with electron-withdrawing groups generates, contrary to expectations, N-tetrachloroallylidene-N′-arylhydrazines instead of 1,1-bisaminated substitution products. The imidoyl-type chlorides are capable of undergoing nucleophilic substitution with amines or hydrides. The resulting compounds should exhibit physiological activity, especially for use in crop science.
    2-硝基五氯丁-1,3-二烯与多种带有吸电子取代基的苯胺反应,出乎意料地生成N-四氯烯丙叉-N'-芳基肼,而不是1,1-双氨取代产物。这类亚胺型氯化物能够与胺或氢化物发生亲核取代反应。生成的化合物应具有生理活性,特别是在作物科学中的应用。
  • Contribution a l'etude de la transformation thermique des aldazines α-ethyleniques. nouvelle voie d'acces aux pyrazoles halogenes ou substitues par des groupements phenoxy, thiophenoxy et thioethoxy en 3(5)
    作者:P. Freche、A. Gorgues、E. Levas
    DOI:10.1016/0040-4020(77)80315-3
    日期:——
    Azines of β-halogen-, aryloxy-, alkylthio- and arylthio-substituted acroleines when heated gave pyrazole derivatives which may be hydrolysed very easily to give N-unsubstituted pyrazoles bearing in the 3(5) position halogen, ArO, RS or ArS groups. The observed heterocyclisation was compared with thermal decomposition of cinnamald azine for which an ionic mechanism had been previously proposed, whereas
    β-卤素,芳氧基,烷硫基和芳硫基取代的丙烯醛在加热时会生成吡唑衍生物,吡唑衍生物很容易被水解,从而生成在3(5)位卤素,ArO,RS或ArS基团的N-未取代的吡唑。将观察到的杂环化与肉桂醛的热分解进行了比较,肉桂醛的热分解先前已提出了离子机制,而我们证明所涉及的机制是内部的1,4-加成,并且根据迁移基团的性质,热分解[ 1,3]或[1,5]σ重排。
  • Chemistry of Polyhalogenated Nitrobutadienes, Part 9: Acyclic and Heterocyclic Nitroenamines and Nitroimines from 2-Nitroperchlorobuta-1,3-diene
    作者:Viktor A. Zapol’skii、Jan C. Namyslo、Mimoza Gjikaj、Dieter E. Kaufmann
    DOI:10.1515/znb-2010-0710
    日期:2010.7.1
    exceedingly versatile 2-nitroperchlorobutadiene (1) gave structurally interesting and physiologically promising nitro-enamines, -imines, -amidines, and hydrazines as well as ring closure reaction products, e. g. pyrimidines and pyrazoles. Most of these reactions turned out to be highly selective with good to very good yields. The structure of the pyrazole precursor (E,E)-1-(benzotriazol-1-yl)-4,4-dichloro-3-
    衍生自极其通用的 2-硝基全氯丁二烯 (1) 的各种氨基、二氨基、氨基硫代或苯并三唑并化合物提供了结构有趣且生理学上有前景的硝基烯胺、-亚胺、-脒和肼以及闭环反应产物,例如嘧啶和吡唑类。大多数这些反应被证明是高度选择性的,产率非常好。吡唑前体(E,E)-1-(benzotriazol-1-yl)-4,4-dichloro-3-(4-ethoxyphenylamino)-1-(4-ethoxyphenylimino)-2-nitrobut-2-的结构单晶 X 射线衍射分析证实了 ene (30) 由于其特殊的取代模式。多卤化硝基丁二烯的图形摘要化学,第 9 部分:来自 2-Nitroperchlorobuta-1,3-diene 的无环和杂环硝基烯胺和硝基亚胺
  • Dihydropyridine derivatives and their production, formulation and use as pharmaceuticals
    申请人:FISONS plc
    公开号:EP0174071A2
    公开(公告)日:1986-03-12
    There are described compounds of formula I, in which R2 and R3, which may be the same or different, each represent alkyl C1 to 6 or cycloalkyl C3 to 8, R7 and R8, which may be the same or different, each represent alkyl C1 to 6 optionally substituted by halogen, and X, Y and Z, which may be the same or different, are each hydrogen, halogen, nitro or alkyl C1 to 6 optionally substituted by halogen, or Z is as defined above and X and Y, together with the carbon atoms to which they are attached, form a C5 to 8 carbocyclic ring, other than a benzene ring, provided that when R2, R3, R7 and R8 are all methyl and X and Z are hydrogen; or when R2 and R3 are both ethyl, R7 and R8 are both methyl and X and Z are hydrogen; then Y is other I than methyl. There are also described methods for making the compounds and their formulation and use as pharmaceuticals, e.g. for the treatment of cardiovascular conditions.
    所述化合物为式 I、 其中 R2 和 R3 可以相同或不同,各自代表 C1-6 烷基或 C3-8 环烷基、 R7 和 R8(可以相同或不同)各自代表 C1-6 烷基,可选被卤素取代,以及 X、Y 和 Z(可以相同或不同)各自为氢、卤素、硝基或任选被卤素取代的 C1 至 6 烷基,或 Z 如上文所定义,且 X 和 Y 与它们所连接的碳原子一起形成 C5 至 8 碳环(苯环除外)、 条件是当 R2、R3、R7 和 R8 均为甲基,且 X 和 Z 均为氢时;或当 R2 和 R3 均为乙基,R7 和 R8 均为甲基,且 X 和 Z 均为氢时;则 Y 为甲基以外的其他 I。 此外,还介绍了这些化合物的制造方法及其配制和用作药物的方法,例如用于治疗心血管疾病。
  • N-aryl-3-aryl-4-substituted-4,5-dihydro-1H-pyrazole-1-carboxamides and processes for their production
    申请人:ROHM AND HAAS COMPANY
    公开号:EP0466408A1
    公开(公告)日:1992-01-15
    This invention relates to novel N-aryl-3-aryl-4-substituted-4,5- dihydro-1H-pyrazole-1-carboxamide compounds which are useful as pesticides, compositions containing those compounds, method of controlling pests and process for preparing these compounds.
    本发明涉及可用作杀虫剂的新型 N-芳基-3-芳基-4-取代-4,5-二氢-1H-吡唑-1-甲酰胺化合物、含有这些化合物的组合物、防治害虫的方法以及制备这些化合物的工艺。
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