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Δ1(6)-2,5-dioxabicyclo<4.4.0.>decene | 114347-18-1

中文名称
——
中文别名
——
英文名称
Δ1(6)-2,5-dioxabicyclo<4.4.0.>decene
英文别名
2,5-dioxabicyclo<4.4.0>dec-1(6)-ene;2,5-dioxabicyclo[4.4.0]dec-1(6)-ene;2,3,5,6,7,8-Hexahydro-1,4-benzodioxine
Δ<sup>1(6)</sup>-2,5-dioxabicyclo<4.4.0.>decene化学式
CAS
114347-18-1
化学式
C8H12O2
mdl
——
分子量
140.182
InChiKey
CKFXBYNDTGHFKT-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:
    217.4±20.0 °C(Predicted)
  • 密度:
    1.08±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.75
  • 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:
    描述:
    三溴甲烷Δ1(6)-2,5-dioxabicyclo<4.4.0.>decenesodium hydroxide苄基三乙基氯化铵 作用下, 以 乙醇二氯甲烷 为溶剂, 反应 48.0h, 以82%的产率得到11,11-dibromo-2,5-dioxabicyclo<4.4.1>propellane
    参考文献:
    名称:
    Fjeldskaar, Inger Reidun; Skatteboel, Lars, Acta Chemica Scandinavica, 1991, vol. 45, # 4, p. 410 - 417
    摘要:
    DOI:
  • 作为产物:
    描述:
    乙二醇2-羟基环己酮二聚物对甲苯磺酸 作用下, 以 为溶剂, 反应 10.0h, 以90%的产率得到Δ1(6)-2,5-dioxabicyclo<4.4.0.>decene
    参考文献:
    名称:
    Fjeldskaar, Inger Reidun; Rongved, Paul; Skatteboel, Lars, Acta chemica Scandinavica. Series B: Organic chemistry and biochemistry, 1987, vol. 41, # 7, p. 477 - 486
    摘要:
    DOI:
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文献信息

  • ACRYLATE ESTER DERIVATIVES AND POLYMER COMPOUNDS
    申请人:Nakayama Osamu
    公开号:US20110060112A1
    公开(公告)日:2011-03-10
    Provided are 1) a polymer which is excellent in a reactivity to acid and a heat stability and which is less swollen in developing, 2) a compound shown below which is a raw material for the above polymer and 3) a photoresist composition which contains the above polymer and which is improved in LWR and excellent in a heat resistance. (wherein n represents an integer of 0 to 2; R 1 represents a hydrogen atom, methyl or the like; R 2 to R 10 each represent independently a hydrogen atom, a linear alkyl group, a branched alkyl group or the like; and A and B each represent independently an oxygen atom or a sulfur atom).
    提供了以下内容:1)一种对酸反应性和热稳定性优异、在显影时膨胀较少的聚合物;2)下面所示的一种上述聚合物的原材料化合物;3)一种包含上述聚合物并在LWR方面得到改善且具有优异耐热性的光阻组合物。(其中,n表示0到2之间的整数;R1表示氢原子、甲基或类似物;R2到R10各自独立地表示氢原子、线性烷基、支链烷基或类似物;A和B各自独立地表示氧原子或硫原子)。
  • [EN] PAK INHIBITORS FOR THE TREATMENT OF CANCER<br/>[FR] INHIBITEURS DE PAK DESTINÉS AU TRAITEMENT DU CANCER
    申请人:AFRAXIS INC
    公开号:WO2013086451A2
    公开(公告)日:2013-06-13
  • Electrochemical transformations of monooxa- and dioxabicycloalkenes and-bicycloalkanes
    作者:Yu. N. Ogibin、A. O. Terent'ev、A. I. Ilovaisky、G. I. Nikishin
    DOI:10.1007/bf02494854
    日期:1999.11
    Electrolysis of 2-oxa- and 2,5-dioxabicyclo[n.4.0]alk-1(6)-enes (n = 4, 10) under conditions of direct undivided anodic oxidation in methanol results in their electrochemical mono- and dimethoxylation; electrolysis of the corresponding 2-oxa- and 2,5-dioxabicycloalkanes involves electrochemical cleavage of the bridging carbon-carbon bonds followed by electrooxidative transformation into methyl omega-(2-methoxytetrahydrofuryl)-, omega-(dimethoxymethyl)-, and omega-(1,3-dioxolan-2-yl)alkanoates.
  • FJELDSKAAR, INGER REIDUN;SKATTEBOL, LARS, ACTA CHEM. SCAND., 45,(1991) N, C. 410-417
    作者:FJELDSKAAR, INGER REIDUN、SKATTEBOL, LARS
    DOI:——
    日期:——
  • FJELDSKAAR, INGER REIDUN;RONGVED, RAUL;SKATTEVZHUSTOL, LARS, ACTA CHEM. SCAND., 41,(1987) N 7, 474-486
    作者:FJELDSKAAR, INGER REIDUN、RONGVED, RAUL、SKATTEVZHUSTOL, LARS
    DOI:——
    日期:——
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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