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2-甲基-5,6-二氢-1,4-二恶英 | 3973-22-6

中文名称
2-甲基-5,6-二氢-1,4-二恶英
中文别名
2,3-二氢-5-甲基[1,4]二氢芑
英文名称
5-methyl-2,3-dihydro-[1,4]dioxine
英文别名
5-Methyl-2,3-dihydro-[1,4]dioxin;2,3-dihydro-5-methyl-1,4-dioxin;5-methyl-2,3-dihydro-1,4-dioxine
2-甲基-5,6-二氢-1,4-二恶英化学式
CAS
3973-22-6
化学式
C5H8O2
mdl
——
分子量
100.117
InChiKey
DGZFPEFJNUNGAL-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:
    114-115 °C
  • 密度:
    0.9828 g/cm3
  • 稳定性/保质期:

    存在于主流烟气中。

计算性质

  • 辛醇/水分配系数(LogP):
    0.6
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.6
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Synthesis and Antifungal Activity of 5,6-Dihydro-3- methyl-1,4-dioxin-2-carboxamides
    摘要:
    Seven N-aryl-5,6-dihydro-3-methyl-1,4-dioxin-2-carboxamides were prepared as potential fungicides. The fungicidal activity of the dioxincarboxamides was evaluated against bean rust, a major disease of cereal crops. Structure-activity relationships for the screened compounds are discussed. The fungicidal activity of the dioxincarboxamides is correlated with that of the structurally similar commercial fungicide, carboxin.
    DOI:
    10.1021/jf970960d
  • 作为产物:
    描述:
    1-(2-hydroxyethoxy)propan-2-ol 在 copper oxide-chromium oxide catalyst 作用下, 生成 2-甲基-5,6-二氢-1,4-二恶英
    参考文献:
    名称:
    Copper Chromite-catalyzed Conversion of Some Glycols to Dioxenes
    摘要:
    DOI:
    10.1021/jo01059a075
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文献信息

  • Thiocarboxylate ester compounds compositions containing the same
    申请人:Uniroyal Chemical Company, Inc.
    公开号:US05268389A1
    公开(公告)日:1993-12-07
    A method of inhibiting the growth or replication of viruses of the HIV group is disclosed. Also disclosed are compounds useful in the method and pharmaceutical formulations incorporating such compounds. The method involves the use of compounds having the general formula: ##STR1## wherein the substituent groups are as defined in the specification.
    本发明揭示了一种抑制HIV病毒群的生长或复制的方法。还揭示了在该方法中有用的化合物以及含有这些化合物的药物配方。该方法涉及使用具有以下一般结构的化合物:##STR1##其中取代基如规范中定义。
  • Nouvelle synthése de dioxènes-1,4
    作者:Cathy Bacquet、Jacques Einhorn、Daniel Lelandais
    DOI:10.1002/jhet.5570170447
    日期:1980.6
    Nous décrivons la synthèse de quelques dioxénes-1,4 connus ou nouveaux à partir des methoxy-2 dioxannes-1,4 correspondants obtenus par voie électrochimique.
    二恶英-1,4合成甲氧基-2二恶英-1,4的通讯员1,44通讯员。
  • Treatment of HIV infections and compounds useful therein
    申请人:Uniroyal Chemical Company, Inc.
    公开号:US05693827A1
    公开(公告)日:1997-12-02
    A method of inhibiting the growth or replication of viruses of the HIV group is disclosed. Also disclosed are compounds useful in the method and pharmaceutical formulations incorporating such compounds. The method involves the use of compounds having the general formula: ##STR1## wherein the substituent groups are as defined in the specification.
    本发明公开了一种抑制HIV病毒组的病毒生长或复制的方法。还公开了在该方法中有用的化合物和包含这些化合物的制药配方。该方法涉及使用具有一般式的化合物:##STR1##其中取代基团如规范中所定义。
  • Catalytic dehydrogenation of dialkylene glycols
    申请人:JEFFERSON CHEM CO INC
    公开号:US02807629A1
    公开(公告)日:1957-09-24
  • Saylor, Richard W.; Sebastian, John F., Synthetic Communications, 1982, vol. 12, # 8, p. 579 - 584
    作者:Saylor, Richard W.、Sebastian, John F.
    DOI:——
    日期:——
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同类化合物

环丙羧酸,2-(羟甲基)-3-甲基-,甲基酯,(1S,2R,3R)- 丙酸,2-甲氧基-,1-(5,6-二氢-1,4-二噁烷-2-基)-2-甲氧基-1-丙烯基酯 三丁基(5,6-二氢-1,4-二恶英-2-基)-锡烷 [1,2]二恶英并[4,3-b]吡啶 5-乙酰基-3,6-二甲基-1,4-二恶英-2(3H)-酮 5-(5,6-二氢-1,4-二氧杂环己烯-2-基)-1,3,4-噁二唑-2-胺 5,6-二氢-[1,4]二恶英-2-羧酸 5,6-二氢-1,4-二恶英-2-甲醛 5,6-二氢-1,4-二恶英-2-甲酰氯 3-甲基-5,6-二氢-1,4-二恶英-2-羧酸 2-甲基-5,6-二氢-1,4-二恶英 2-(5,6-二氢-1,4-二氧-2-基)-4,4,5,5-四甲基-1,3,2-二氧杂硼烷 2-(5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷-2-亚基)-5,6-二氢-1,3-二硫环戊并[4,5-B][1,4]二烷 2,3-二氢-5,6-二甲基-1,4-二恶英 2,2,2-三氟-1-(3-甲基-5,6-二氢-1,4-二恶英-2-基)乙酮 1H,5H-环戊二烯并[5,6][1,4]二恶英并[2,3-d]咪唑 1,4-二氧杂-2-己烯 1,4-二恶英-2-甲酰氯,5,6-二氢-3-甲基-(9CI) 1,4-二恶英 EDO-S,S-DMEDT-TTF 2,3-di(furan-2-yl)-5,6-dihydro-1,4-dioxine 2-(carboxymethyl)-3-(3-oxobutyl)dioxene 2-(carboxymethyl)-trans-5,6-diethyl-3-(3-oxobutyl)dioxene trifluoromethyl dihydro-1,4-dioxin-3-carbonyl chloride 6-bromo-2,3-dihydrobenzo[1,4]dioxine 3,4-(vinylenedioxy)thiophene ethyl 5,6-dihydro-2-trifluoromethyl-1,4-dioxin-3-carboxylate 5,6-dihydro-2-trifluoromethyl-1,4-dioxin-3-carboxylic acid F-2-methyl-2,3-dihydro-1,4-dioxin Phosphorodithioic acid, O,O-diethyl S-(5,6-dihydro-1,4-dioxin-2-yl) ester 2-[4,5-bis(ethylthio)-1,3-dithiol-2-ylidene]-5-(4,5-ethylenedioxy-1,3-dithiol-2-ylidene)-1,3,4,6-tetrathiapentalene Δ1(7)-8,11-dioxabicyclo<5.4.0>undecene 8-ethoxy-2,5-dioxa-7,10-dithiabicyclo<4.4.0>deca-1(6)-ene 2,2,5,5,8,8-Hexamethyl-2,3,5,6,7,8-hexahydro-benzo[1,4]dioxine ethylenedioxytetrathiafulvalenoquinone-1,3-diselenolemethide 1-(5,6-dihydro-[1,4]dioxin-2-yl)-2-isopropyl-propenone 6,7-Dimethyl-2,3-dihydro-1,4-benzodioxine-5,8-dione 3-chlorobenzo[b]fur[3,2-e][1,4]dioxin-2(9aH)-one 4,5-dimethyl-4',5'-ethylenedioxy-2,2'-ethanediylidenebis(1,3-dithiole) 4,5-bis(methylthio)-4',5'-ethylenedioxy-2,2'-ethanediylidenebis(1,3-dithiole) dioxinone 3-(5,6-Dihydro-[1,4]dioxin-2-yl)-cyclohexanone 4,5-ethylenedioxy-4'-methyltetrathiafulvalene (5,6-dihydro-p-dioxin-2-yl)phenylphosphinic acid hexachloro-2,3-dihydro-1,4-dioxin 6,7-Bis(octadecylsulfanyl)-2,3-dihydro-1,4-benzodioxine-5,8-dione 5,6-di-n-octylthio-2,3-ethylenedioxy-1,4-benzoquinone 6-Octadecylsulfanyl-2,3-dihydro-1,4-benzodioxine-5,8-dione 5-n-octylthio-2,3-ethylenedioxy-1,4-benzoquinone 6,7-Bis(dodecylsulfanyl)-2,3-dihydro-1,4-benzodioxine-5,8-dione