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1,4-己烷二醇 | 16432-53-4

中文名称
1,4-己烷二醇
中文别名
——
英文名称
hexane-1,4-diol
英文别名
——
1,4-己烷二醇化学式
CAS
16432-53-4
化学式
C6H14O2
mdl
——
分子量
118.176
InChiKey
QVTWBMUAJHVAIJ-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

  • 熔点:
    26.38°C (estimate)
  • 沸点:
    221.7°C (rough estimate)
  • 密度:
    0.9756

计算性质

  • 辛醇/水分配系数(LogP):
    0.4
  • 重原子数:
    8
  • 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

安全信息

  • 海关编码:
    2905399090

SDS

SDS:c9270ffb08c9d6ce19265a4a9c63f725
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反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Wohlgemuth, Comptes Rendus Hebdomadaires des Seances de l'Academie des Sciences, 1914, vol. 159, p. 80
    摘要:
    DOI:
  • 作为产物:
    描述:
    4-羰基己酸乙酯 在 lithium aluminium tetrahydride 、 乙醚 作用下, 生成 1,4-己烷二醇
    参考文献:
    名称:
    Obolenzew; Bucharow, 1957, p. 9,15
    摘要:
    DOI:
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文献信息

  • METHOD FOR PRODUCING CIS- AND TRANS-ENRICHED MDACH
    申请人:BASF SE
    公开号:US20170260115A1
    公开(公告)日:2017-09-14
    A process for preparing trans-enriched MDACH, including: distilling an MDACH starting mixture in the presence of an auxiliary, which is an organic compound having a molar mass of 62 to 500 g/mol, a boiling point at least 5° C. above the boiling point of cis,cis-2,6-diamino-1-methylcyclohexane, and 2 to 4 functional groups, each of which is independently an alcohol group or a primary, secondary or tertiary amino group. The MDACH starting mixture includes 0 to 100% by weight of 2,4-MDACH and 0 to 100% by weight of 2,6-MDACH, based on the total amount of MDACH present in the MDACH starting mixture. The MDACH starting mixture includes both trans and cis isomers. Trans-enriched MDACH includes 0 to 100% by weight of 2,4-MDACH and 0 to 100% by weight of 2,6-MDACH, where the proportion of trans isomers in the mixture is higher than the proportion of trans isomers in the MDACH starting mixture.
    制备富含反式异构体MDACH的方法,包括:在辅助剂的存在下蒸馏MDACH起始混合物,所述辅助剂是一种有着62至500克/摩尔的摩尔质量、沸点至少比顺式、顺式-2,6-二基-1-甲基环己烷的沸点高出至少5摄氏度,并且具有2至4个官能团,每个官能团独立地是醇基团或一级、二级或三级基团的有机化合物。MDACH起始混合物包括以MDACH起始混合物中MDACH总量为基础的0至100%重量的2,4-MDACH和0至100%重量的2,6-MDACH。MDACH起始混合物包括反式和顺式异构体。富含反式异构体的MDACH包括以2,4-MDACH和2,6-MDACH的0至100%重量为基础,其中混合物中反式异构体的比例高于MDACH起始混合物中反式异构体的比例。
  • [EN] INHIBITORS OF RAF KINASES<br/>[FR] INHIBITEURS DE KINASES RAF
    申请人:KINNATE BIOPHARMA INC
    公开号:WO2020198058A1
    公开(公告)日:2020-10-01
    Provided herein are inhibitors of receptor tyrosine kinase effector, RAF, pharmaceutical compositions comprising said compounds, and methods for using said compounds for the treatment of diseases.
    本文提供了受体酪氨酸激酶效应子RAF的抑制剂,包括所述化合物的药物组合物,以及使用这些化合物治疗疾病的方法。
  • Proline-Catalyzed Knoevenagel Condensation/[4+2] Cycloaddition Cascade Reaction: Application to Formal Synthesis of Averufin
    作者:Haibo Tan、Xinzheng Chen、Huiyu Chen、Hongxin Liu、Shengxiang Qiu
    DOI:10.1002/ejoc.201500559
    日期:2015.8
    A remarkable proline-catalyzed method for the construction of biologically interesting oxygen-bridged tricyclic ketal skeletons was uncovered by starting from a variety of readily available cyclic 1,3-diketones and either 1,4- or 1,5-dicarbonyl substrates. The approach, which mimics a biosynthetic Knoevenagel condensation/[4+2] cycloaddition sequence, establishes a viable synthetic strategy for the
    通过从各种现成的环状 1,3-二酮和 1,4-或 1,5-二羰基底物开始,揭示了一种用于构建具有生物学意义的氧桥连三环缩酮骨架的非凡脯酸催化方法。该方法模拟了生物合成的 Knoevenagel 缩合/[4+2] 环加成序列,为阿鲁芬的有效形式合成建立了可行的合成策略。
  • Switching between Novel Samarium(II)-Mediated Cyclizations by a Simple Change in Alcohol Cosolvent
    作者:Thomas K. Hutton、Kenneth W. Muir、David J. Procter
    DOI:10.1021/ol0358399
    日期:2003.12.1
    undergo two very different stereoselective cyclization reactions mediated by samarium(II) iodide depending upon the alcohol cosolvent used in the reaction. Switching between an unprecedented aldol spirocyclization and a novel cyclobutanol-forming process can be achieved simply by changing the alcohol cosolvent from methanol to tert-butyl alcohol. [reaction: see text]
    根据反应中使用的醇助溶剂,γ-不饱和酮会经历由化sa(II)介导的两个非常不同的立体选择性环化反应。只需将醇助溶剂从甲醇更改为叔丁醇,即可在前所未有的羟醛螺环化和新型环丁醇形成工艺之间进行切换。[反应:看文字]
  • An efficient and reusable vanadium based catalytic system for room temperature oxidation of alcohols to aldehydes and ketones
    作者:Gayatri Sarmah、Saitanya K. Bharadwaj、Anindita Dewan、Ankur Gogoi、Utpal Bora
    DOI:10.1016/j.tetlet.2014.07.047
    日期:2014.9
    A simple and efficient vanadium based catalyst system for the oxidation of primary and secondary alcohols to aldehydes or ketones is reported using tert-butyl hydroperoxide as oxidizing agent and vanadyl sulfate as catalyst at room temperature. The versatility of the catalytic protocol is studied with wide variety of substrates.
    据报道,在室温下,使用叔丁基氢过氧化物作为氧化剂,并使用硫酸氧钒作为催化剂,可以将伯醇和仲醇氧化成醛或酮的简单有效的基催化剂体系。催化方案的多功能性已在多种底物上进行了研究。
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