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3-ethylhexane-3,4-diol | 344244-74-2

中文名称
——
中文别名
——
英文名称
3-ethylhexane-3,4-diol
英文别名
——
3-ethylhexane-3,4-diol化学式
CAS
344244-74-2
化学式
C8H18O2
mdl
——
分子量
146.23
InChiKey
NFSRFJPGZZTLEE-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):
    1.5
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

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文献信息

  • [EN] PROCESS FOR REDUCING THE OXYGEN CONTENT OF BIOMASS USING VANADIUM-BASED CATALYSTS<br/>[FR] PROCÉDÉ POUR RÉDUIRE LA TENEUR EN OXYGÈNE DE LA BIOMASSE À L'AIDE DE CATALYSEURS À BASE DE VANADIUM
    申请人:UNIV DANMARKS TEKNISKE
    公开号:WO2016101958A1
    公开(公告)日:2016-06-30
    The present invention concerns a process for converting biomass into useful organic building blocks for the chemical industry. The process involves the use of vanadium-based catalysts of the formula Aα+a(VvXxR1yR2z)α*a-, which may be readily prepared from industrial vanadium compounds, for converting a polyol in a solvent.
    这项发明涉及将生物质转化为化工行业有用的有机建筑模块的过程。该过程涉及使用具有公式Aα+a(VvXxR1yR2z)α*a-的基于钒的催化剂,这些催化剂可以从工业钒化合物中方便地制备出来,用于将多元醇在溶剂中转化。
  • METHOD FOR PRODUCING NON-ISOCYANATE POLYURETHANES
    申请人:Henkel AG & Co. KGaA
    公开号:US20210324141A1
    公开(公告)日:2021-10-21
    The present application is directed to a method for producing non-isocyanate polyurethanes. More particularly, the application is directed to method for producing non-isocyanate polyurethanes by using a single catalyst component selected from an amidoindole derivative, a benzimidazole derivative and a squaramide derivative.
    本申请涉及一种生产非异氰酸酯聚氨酯的方法。更具体地说,该申请涉及一种通过使用从酰胺吲哚衍生物、苯并咪唑衍生物和方酰胺衍生物中选择的单一催化剂组分来生产非异氰酸酯聚氨酯的方法。
  • [EN] ESTER SYNTHESIS USING HETEROGENEOUS AU/TIO2 CATALYST<br/>[FR] SYNTHÈSE D'ESTER À L'AIDE D'UN CATALYSEUR AU/TIO2 HÉTÉROGÈNE
    申请人:EASTMAN CHEM CO
    公开号:WO2020102124A1
    公开(公告)日:2020-05-22
    A process for direct esterification of an alkyl aldehyde with an alkyl alcohol to produce an alkyl ester is disclosed. The process comprises reacting an alkyl aldehyde with an alkyl alcohol in the presence of an Au/TiOa catalyst, a base and an enal or oxygen to form an ester and an aldehyde. The process avoids liberation of water and avoids the step of oxidation of the alkyl aldehyde to an alkyl acid.
    公开了一种通过将烷基醛与烷基醇直接酯化以产生烷基酯的方法。该过程包括在Au/TiOa催化剂、碱和烯醛或氧的存在下,使烷基醛与烷基醇反应,形成酯和醛。该过程避免了水的释放,并避免了将烷基醛氧化为烷基酸的步骤。
  • Phenyl-furan compounds as vitamin d receptor modulators
    申请人:Gajewski Peter Robert
    公开号:US20070105951A1
    公开(公告)日:2007-05-10
    The present invention relates to novel, non-secosteroidal, phenyl-furan compounds with vitamin D receptor (VDR) modulating activity that are less hypercalcemic than 1α,25dihydroxy vitamin D3. These compounds are useful for treating bone disease and psoriasis.
    本发明涉及一种新型的非次生类固醇苯基呋喃化合物,具有维生素D受体(VDR)调节活性,其低于1α,25-二羟基维生素D3的高钙血症作用。这些化合物可用于治疗骨病和牛皮癣。
  • Substituted cycloalkene derivative
    申请人:Daiichi Sankyo Company, Limited
    公开号:US07935835B2
    公开(公告)日:2011-05-03
    A compound of formula (I) Wherein X, Y, ring A, ring B, l, m, R1, R2, R4 and R5 are as defined herein, to supress intracellular signal transduction or cell activation induced by endotoxin and to suppress cell responses due to the intracellular signal transduction and cell activation such as an excess generation of inflammatory mediators such as TNF-α, pharmacologically acceptable salts therefor, a preparation method therefor, and a medicament containing the aforementioned substituted cycloalkene derivative as an active ingredient which is superior in prophylaxis and/or treatment of diseases such as sepsis (septic shock, disseminated intravascular coagulation, multiple organ failure and the like), that are associated with intracellular signal transduction or cell activation induced by endotoxin and to cell responses to the intracellular signal transduction and cell activation.
    一种化合物的化学式为(I),其中X、Y、环A、环B、l、m、R1、R2、R4和R5的定义如本文所述,用于抑制内毒素诱导的细胞内信号转导或细胞激活,并抑制由于细胞内信号转导和细胞激活引起的细胞反应,例如过度产生炎症介质如TNF-α,其药理学上可接受的盐,其制备方法,以及包含上述取代环戊烯衍生物作为活性成分的药物制剂,其在预防和/或治疗诸如败血症(脓毒症休克、弥漫性血管内凝血、多器官衰竭等)等与内毒素诱导的细胞内信号转导或细胞激活以及对细胞内信号转导和细胞激活的细胞反应有关的疾病方面具有卓越的预防和/或治疗作用。
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