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2,6-Dimethyl-1,4-dioxene | 3973-23-7

中文名称
——
中文别名
——
英文名称
2,6-Dimethyl-1,4-dioxene
英文别名
2,6-Dimethyl-1,4-dioxen;2,6-Dimethyl-1,4-dioxen-2;2,6-Dimethyl-1,4-dioxan;2,6-dimethyl-2,3-dihydro-[1,4]dioxine;2,6-Dimethyl-2,3-dihydro-[1,4]dioxin;2,6-dimethyl-2,3-dehydro-1,4-dioxane;2,6-Dimethyl-2,3-dihydro-1,4-dioxine
2,6-Dimethyl-1,4-dioxene化学式
CAS
3973-23-7
化学式
C6H10O2
mdl
——
分子量
114.144
InChiKey
KPWYQLMJBYDCHN-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:
    126-126.5 °C(Press: 749 Torr)
  • 密度:
    0.952±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.67
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    二丙二醇 在 copper oxide-chromium oxide catalyst 作用下, 生成 2,6-Dimethyl-1,4-dioxene
    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

  • ACRYLATE ESTER DERIVATIVES AND POLYMER COMPOUNDS
    申请人:NAKAYAMA Osamu
    公开号:US20120316349A1
    公开(公告)日:2012-12-13
    A cyclic alcohol of formula (II-1): wherein: R 2 , R 3 , and R 4 are each independently a hydrogen atom, a linear alkyl group comprising 1 to 6 carbon atoms, a branched alkyl group comprising 3 to 6 carbon atoms, or a cyclic alkyl group comprising 3 to 6 carbon atoms; or R 2 and R 3 or R 3 and R 4 combine to form an alkylene group comprising 3 to 6 carbon atoms; m is 1 or 2; R 5 , R 6 , R 7 , R 8 , R 9 , and R 10 are each independently a hydrogen atom, a linear alkyl group comprising 1 to 6 carbon atoms, a branched alkyl group comprising 3 to 6 carbon atoms, or a cyclic alkyl group comprising 3 to 6 carbon atoms; A is an oxygen atom; and B is an oxygen atom or a sulfur atom. In addition, a process for producing the cyclic alcohol of formula (II-1).
    一种化学式为(II-1)的环状醇:其中:R2、R3和R4分别独立地是氢原子、由1至6个碳原子组成的直链烷基基团、由3至6个碳原子组成的支链烷基基团或由3至6个碳原子组成的环状烷基基团;或者R2和R3或R3和R4结合形成由3至6个碳原子组成的亚烯基基团;m为1或2;R5、R6、R7、R8、R9和R10分别独立地是氢原子、由1至6个碳原子组成的直链烷基基团、由3至6个碳原子组成的支链烷基基团或由3至6个碳原子组成的环状烷基基团;A为氧原子;B为氧原子或硫原子。此外,一种制备化学式(II-1)的环状醇的方法。
  • Catalytic dehydrogenation of dialkylene glycols
    申请人:JEFFERSON CHEM CO INC
    公开号:US02807629A1
    公开(公告)日:1957-09-24
  • KARAEV, S. F.;MAMEDOV, EH. A.;GARAEVA, SH. V., IZV. VUZOV. XIMIYA I XIM. TEXNOL., 1951, 28, N 5, 117-118
    作者:KARAEV, S. F.、MAMEDOV, EH. A.、GARAEVA, SH. V.
    DOI:——
    日期:——
  • US8431722B2
    申请人:——
    公开号:US8431722B2
    公开(公告)日:2013-04-30
  • US8362169B2
    申请人:——
    公开号:US8362169B2
    公开(公告)日:2013-01-29
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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