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ditropylether | 16273-47-5

中文名称
——
中文别名
——
英文名称
ditropylether
英文别名
di-7-cycloheptatrienyl ether;di-cyclohepta-2,4,6-trienyl ether;Di-cyclohepta-2,4,6-trienyl-aether;Bis--ether;Di--ether;Ditropylaether;7-Cyclohepta-2,4,6-trien-1-yloxycyclohepta-1,3,5-triene
ditropylether化学式
CAS
16273-47-5
化学式
C14H14O
mdl
——
分子量
198.265
InChiKey
KNFQDAOJJNEQEQ-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:
    341.0±11.0 °C(Predicted)
  • 密度:
    1.04±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.1
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

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

  • 作为反应物:
    描述:
    ditropylether三氟乙酸 作用下, 以 氘代氯仿 为溶剂, 反应 3.0h, 生成 环庚三烯酮环庚三烯
    参考文献:
    名称:
    NMR光谱法明确检测2,4,6-环庚三烯-1-醇并用苯基三唑啉二酮捕获
    摘要:
    首次通过NMR光谱法明确地检测出标题醇3作为过渡中间体,导致水溶液中对yl离子(5)与氢氧根离子之间的阳离子-阴离子反应中的二tropylether(6)。人们还发现,6给出3中的酸催化歧化瞬态产物6成环庚三烯酮的混合物(4)和1,3,5-环庚三烯(7在含有水氯仿)。再者3的存在在后者的反应通过用4-苯基-1,2,4-三唑啉-3,5-二酮捕集得到的norcaradiene形式的[4 + 2]环加成确认3。
    DOI:
    10.1016/s0040-4020(02)01617-4
  • 作为产物:
    描述:
    alkaline earth salt of/the/ methylsulfuric acid 在 sodium hydroxide 作用下, 生成 ditropylether
    参考文献:
    名称:
    Bryce-Smith; Perkins, Chemistry and industry, 1959, p. 1022
    摘要:
    DOI:
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文献信息

  • ter Borg,A.P. et al., Recueil des Travaux Chimiques des Pays-Bas, 1962, vol. 81, p. 177 - 184
    作者:ter Borg,A.P. et al.
    DOI:——
    日期:——
  • Long-term treatment of focal segmental glomerulosclerosis in children with cyclosporine given as a single daily dose
    作者:Aftab S. Chishti、Jonathan M. Sorof、Eileen D. Brewer、Arundhati S. Kale
    DOI:10.1053/ajkd.2001.27692
    日期:2001.10
    Cyclosporine (CsA) has been successfully used for treatment of children with focal segmental glomerulosclerosis (FSGS) and nephrotic syndrome (NS) for the last decade. Response rates of 50% to 100% have been reported using twice-daily dosing of 5 to 32 mg/kg/d, achieving trough blood levels of 70 to 500 ng/mL. Treatment has been associated with a high incidence of side effects, including nephrotoxicity, hypertension, gingival hyperplasia, and hirsutism. To determine whether once-daily low-dose CsA could minimize side effects and still induce remission, 21 children with biopsy-proven FSGS and NS, each treated with CsA, 4.6 +/- 0.8 mg/kg/d, with no predetermined target trough blood levels, were studied. Eleven of 21 children (52%) attained complete remission and 5 of 21 children (24%) attained partial remission, for a total response rate of 76%. Mean time to response was 2.8 +/- 0.8 months, and mean duration of therapy was 20.6 +/- 13.7 months. CsA dosage was tapered or stopped in 9 responders; 3 of these patients maintained remission at last follow-up 6 to 13 months later, and 6 patients relapsed at 1.5 to 18.7 months (mean, 8.7 months). Five of these 6 patients responded again when CsA therapy was restarted or the dosage was increased. Twelve of 16 responders were still being administered CsA at last follow-up 11 to 60 months (mean, 24.6 months) later. Five of 21 patients (24%) had no response to CsA during 2 to 27 months of therapy; 4 of these 5 patients developed end-stage renal disease after CsA therapy was stopped. Side effects of CsA therapy were minimal: 1 patient each developed new-onset hypertension or gingival hyperplasia, and no patient had hirsutism or nephrotoxicity. Single daily low-dose CsA appears to be effective for long-term treatment of children with FSGS and NS, with fewer side effects than twice-daily dosing. (C) 2001 by the National Kidney Foundation, Inc.
  • terBorg; Kloosterziel, Recueil des Travaux Chimiques des Pays-Bas, 1963, vol. 82, p. 741,754
    作者:terBorg、Kloosterziel
    DOI:——
    日期:——
  • Vol'pin,M.E. et al., Journal of general chemistry of the USSR, 1960, vol. 30, p. 170 - 173
    作者:Vol'pin,M.E. et al.
    DOI:——
    日期:——
  • Orlando; Weiss, Journal of Organic Chemistry, 1962, vol. 27, p. 4714 Anm. 6
    作者:Orlando、Weiss
    DOI:——
    日期:——
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