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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-氧硫杂环己烷-3-羧酸4,4-二氧化物 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 2-(2,2,2-trifluoro-1-trifluoromethyl-ethylidene)-3,6-dihydro-2H-pyran ethylenedioxodiselenadithiafulvalene (E)-N-benzyl-2-(2-(furan-2-yl)vinyl)-4,5-dihydrofuran-3-carboxamide 4-(2-(5,6-Dihydro-[1,3]dithiolo[4,5-b][1,4]dioxin-2-ylidene)-1,3-dithiol-4-yl)pyridine 1,3,4,5-Tetrakis-(trifluoromethyl)-6,7-dimethyl-2-oxabicyclo<3.2.0>hepta-3,6-dien 2,4-Bis-(hexafluoroisopropyliden)-1,3-dioxolan 6,9-Dichlorospiro[2,4-dihydro-[1,4]dioxepino[2,3-d]pyridazine-3,1'-cyclopentane] 3-acetoxymethyl-(3ar,7at)-hexahydro-benzooxazole-2-thione 1-(2-methyl-5,6-dihydro-[1,4]oxathiin-3-yl)-ethanone 2,3-dihydro-9H-cyclohept<1,2-b>-1,4-oxathiin 4-[5-(4,5-Bis-methylselanyl-[1,3]dithiol-2-ylidene)-[1,3]dithiolo[4,5-d][1,3]dithiol-2-ylidene]-tetrahydro-pyran 1-(5,6-Dihydro-1,4-dioxin-2-yl)-3-methyl-1-butanone 2H-arsinino[4,3-b]pyran 2,2-Diaethyl-3,4,5,6-tetrachlor-2H-pyran (5-Chloromethyl-4,5-dihydro-furan-3-yl)-phosphonic acid dibutyl ester (5,6-dihydro-p-dioxin-2-yl)phosphonic acid 2-(2(5H)-furanylidene)-5-methyltetrahydrofuran 2,4-dichloro-4-dioxolan-2-ylidene-3-oxobutanenitrile 4,5-dichloro-4',5'-ethylenedioxytetrathiafulvalene 4,4,6-trimethyl-2-(2,4,4,6-tetramethyl-[1,3]oxazinan-2-ylmethyl)-5,6-dihydro-4H-[1,3]oxazine 4',5'-dimethyl-EDO-TTF 2-<2-(1,4-dioxenyl)>-1-propene 4,5-ethylenedioxy-4'-iodotetrathiafulvalene N-(1,2,2,2-tetrachloroethyl)-5,6-dihydro-2-methyl-1,4-oxathiin-3-carboxamide (2-(5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dioxin-2-ylidene)-1,3-dithiol-4-yl)trimethylstannane 2-(2,4,6,8-tetrathia-10,13-diselenatricyclo[7.4.0.03,7]trideca-1(9),3(7)-dien-5-ylidene)-5,6-dihydro-[1,3]dithiolo[4,5-b][1,4]dioxine 1-(5,6-Dihydro-[1,4]dioxin-2-yl)-2-methyl-propan-1-one 4,5-diiodo-4',5'-ethylenedioxytetrathiafulvalene Ethylenedioxymethylenediselenotetrathiafulvalene