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methanol diethyl ether | 65334-65-8

中文名称
——
中文别名
——
英文名称
methanol diethyl ether
英文别名
methanol ethyl ether;Diethyl ether methanol;ethoxyethane;methanol
methanol diethyl ether化学式
CAS
65334-65-8
化学式
CH4O*C4H10O
mdl
MFCD00144265
分子量
106.165
InChiKey
MDKXBBPLEGPIRI-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.84
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    7,9-dibenzyl-3,4-dihydro-2H,6H-pyrimido[6,1-b][1,3]thiazine-6,8(7H)-dione 、 methanol diethyl ether三溴化硼 作用下, 以 甲醇甲苯 为溶剂, 以4.88 g (71.1%, light white crystal)的产率得到9-benzyl-3,4-dihydro-2H,6H-pyrimido[6,1-b][1,3]thiazine-6,8(7H)-dione
    参考文献:
    名称:
    Imidazopyridine or imidazopyrimidine compounds, their production and use
    摘要:
    这项发明提供了一种新的具有抑制粘附分子表达活性的缩合咪唑化合物。该发明还提供了一种治疗和预防糖尿病肾病和/或自身免疫疾病的药剂,以及一种用于器官移植的免疫抑制剂。
    公开号:
    US05840732A1
  • 作为试剂:
    描述:
    2-Morpholino-2-(2-pyridyl)-thioacetamid吗啉聚合甲醛methanol diethyl ether 作用下, 以 甲醇 为溶剂, 反应 20.0h, 以to give 2-morpholino-N-morpholinomethyl-2-(2-pyridyl)thioacetamide, m.p. 144°-147°C. (dec.)的产率得到2-Morpholino-N-morpholinomethyl-2-(2-pyridyl)-thioacetamid
    参考文献:
    名称:
    N-aminomethyl-2-amino(and 2-amino-methyl)-2-(2-quinolyl)-thioacetamides
    摘要:
    这些化合物是N-氨甲基-2-氨基(和2-氨甲基)-2-杂环硫代乙酰胺,它们是胃酸分泌抑制剂。
    公开号:
    US03933811A1
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文献信息

  • Benzylamine derivatives which are useful in treating psychiatric
    申请人:Akzo Nobel, N.V.
    公开号:US06080773A1
    公开(公告)日:2000-06-27
    The present invention relates to certain novel benzylamine derivatives, to processes for their preparation, to pharmaceutical formulations containing them and to their use in medical therapy, particularly in the treatment of depression.
    本发明涉及某些新颖的苯甲基胺衍生物,其制备方法,含有它们的药物制剂及其在医疗治疗中的用途,特别是在抑郁症治疗中的用途。
  • N-oxides of amino containing pyrido \x9b2,3-D! pyrimidines
    申请人:Warner-Lambert Company
    公开号:US05945422A1
    公开(公告)日:1999-08-31
    N-oxides of amino containing 6-aryl pyrido\x9b2,3-d!-pyrimidine 7-imines, 7-ones, and 7-thiones have the formula ##STR1## where A and B are linkers, Ar is aryl, R.sub.2 is aklyl, X is O, S, or NH, or NAcyl, and R.sub.5 and R.sub.6 are alkyl. The compounds are inhibitors of protein tyrosine kinases and cyclin-dependent kinases, and are thus useful in treating cellular proliferation mediated thereby. The compounds are especially useful in treating cancer, atherosclerosis, restenosis, and psoriasis.
    含有6-芳基吡啶\x9b2,3-d!-嘧啶7-亚胺、7-酮和7-硫醚的N-氧化物的化学式为##STR1##其中A和B是连接剂,Ar是芳基,R.sub.2是烷基,X是O、S或NH,或NAcyl,R.sub.5和R.sub.6是烷基。这些化合物是蛋白酪氨酸激酶和细胞周期依赖性激酶的抑制剂,因此在治疗由此介导的细胞增殖方面非常有用。这些化合物在治疗癌症、动脉粥样硬化、再狭窄和牛皮癣方面特别有用。
  • Glutaminase inhibitory compounds, compositions, and methods of use
    申请人:Takeda Chemical Industries, Ltd.
    公开号:US05552427A1
    公开(公告)日:1996-09-03
    There is disclosed a pharmaceutical composition for inhibiting glutaminase which comprises a imidazole derivative or a salt thereof. This compound selectively inhibits the proliferation of tumor cells, and the composition is useful as an anti-cancer agent. There is also disclosed a imidazole derivative having glutaminase inhibitory activity.
    揭示了一种用于抑制谷氨酸酶的药物组合物,包括一种咪唑衍生物或其盐。该化合物选择性地抑制肿瘤细胞的增殖,该组合物可用作抗癌剂。还揭示了一种具有谷氨酸酶抑制活性的咪唑衍生物。
  • Quinoline derivatives or salt thereof and remedy for cardiac diseases
    申请人:Kowa Co., Ltd.
    公开号:US05576324A1
    公开(公告)日:1996-11-19
    A quinoline derivative represented by general formula (1), a medicinally acceptable salt thereof, and a remedy for cardiac diseases containing the same: ##STR1## [wherein ring A represents a furan, dihydrofuran or dioxolane ring, and R.sup.1 represents an aminoalkyl group]. The compound (1) has a positively inotropic effect on myocardia and an antiarrhythmic effect, and can dilate blood vessels without extremely increasing the heart rate. Therefore, a remedy for cardiac diseases containing the same as the active ingredient is remarkably useful for treating cardiac insufficiency, arrhythmia, and so forth.
    一种以一般式(1)表示的喹啉衍生物,其药学上可接受的盐,以及含有该物质的心脏疾病疗法:##STR1## [其中环A代表呋喃、二氢呋喃或二氧杂环戊烷环,R.sup.1代表氨基烷基基团]。化合物(1)对心肌具有正性肌力作用和抗心律失常作用,并且可以扩张血管而不会极大增加心率。因此,含有该物质作为活性成分的心脏疾病疗法对治疗心脏功能不全、心律失常等疾病非常有用。
  • 2-(3-Amino-2-hydroxy-propoxy)-mono-and diazines
    申请人:Ciba-Geigy Corporation
    公开号:US04410530A1
    公开(公告)日:1983-10-18
    Heterocyclic compounds of the formula ##STR1## wherein Het denotes optionally substituted pyridazinyl, pyrimidinyl, pyrazinyl or substituted pyridyl, R.sub.1 is hydrogen or methyl and R.sub.2 is lower alklyl, optionally substituted phenyl-lower alkyl, carboxy-lower alkyl or functionally modified carboxy-lower alkyl, their condensation products with aldehydes, ketones or carbonic acid and their N-oxides, which are valuable (cardioselective) .beta.-receptor blocking agents, and/or (cardioselective) .beta.-receptor-stimulants.
    式为##STR1##的杂环化合物,其中Het表示可选择地取代的吡啶啉基、嘧啶基、吡嗪基或取代的吡啶基,R.sub.1为氢或甲基,R.sub.2为低碳链基、可选择地取代的苯基-低碳链基、羧基-低碳链基或功能性改性的羧基-低碳链基,它们与醛、酮或碳酸的缩合产物以及它们的N-氧化物,是有价值的(心脏选择性的)β-受体阻滞剂和/或(心脏选择性的)β-受体激动剂。
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