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4,7-癸二醇 | 4469-89-0

中文名称
4,7-癸二醇
中文别名
——
英文名称
4,7-decanediol
英文别名
decane-4,7-diol
4,7-癸二醇化学式
CAS
4469-89-0
化学式
C10H22O2
mdl
——
分子量
174.283
InChiKey
MBEWGVZBETVWKJ-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):
    2.3
  • 重原子数:
    12
  • 可旋转键数:
    7
  • 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

SDS

SDS:0edbd1b02804245040791f132f1ff25f
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • Biocatalytic synthesis of non-vicinal aliphatic diols
    作者:Ana C. Ebrecht、Jasmin C. Aschenbrenner、Martha S. Smit、Diederik J. Opperman
    DOI:10.1039/d0ob02086a
    日期:——
    Biocatalysts are receiving increased attention in the field of selective oxyfunctionalization of C–H bonds, with cytochrome P450 monooxygenases (CYP450s), and the related peroxygenases, leading the field. Here we report on the substrate promiscuity of CYP505A30, previously characterized as a fatty acid hydroxylase. In addition to its regioselective oxyfunctionalization of saturated fatty acids (ω-1
    在细胞色素P450单加氧酶(CYP450s)和相关的过加氧酶的C–H键选择性加氧官能化领域,生物催化剂受到了越来越多的关注,并引领了该领域。在这里我们报告CYP505A30的底物滥交,以前被表征为脂肪酸羟化酶。除了饱和脂肪酸的区域选择性氧官能化(ω-1–ω-3羟基化)以外,伯脂肪醇也具有相似的区域选择性。此外,烷烃如正辛烷和正癸烷也容易被接受,从而允许通过顺序的氧合产生非邻位二醇。
  • Novel asymmetric phosphine ligand
    申请人:——
    公开号:US20030139285A1
    公开(公告)日:2003-07-24
    A phosphine compound having excellent properties (chemical selectivity, enantioselectivity, catalytic activity) as a catalyst for asymmetric syntheses, especially asymmetric hydrogenations. A phosphine-phospholane compound represented by the following formula (1): 1 a phosphine-primary phosphine intermediate; a transition metal complex including the phosphine-phospholane compound of formula (1) and a transition metal, and a catalyst including the transition metal complex.
    一种磷化合物,具有优异的性质(化学选择性、对映选择性、催化活性),作为不对称合成催化剂,特别是不对称氢化反应催化剂。该磷-磷杂环化合物的化学式表示为(1):1a 磷-一级磷中间体;包括化学式为(1)的磷-磷杂环化合物和过渡金属的过渡金属配合物,以及包括过渡金属配合物的催化剂。
  • NOVEL ASYMMETRIC PHOSPHINE LIGAND
    申请人:——
    公开号:US20030144138A1
    公开(公告)日:2003-07-31
    A novel phosphine compound having excellent properties (chemical selectivity, enantioselectivity, catalytic activity) as a catalyst for asymmetric syntheses, especially asymmetric hydrogenation. A phosphine-phosphorane compound represented by the following general formula: 1 (wherein R 1 represents hydrogen atom or a linear or branched alkyl group having 1 to 4 carbon atoms, R 2 , R 3 , R 4 , and R 5 are the same or different, and each represents hydrogen atom, or an alkyl group having 1 to 6 carbon atoms, etc., and each of R 2 and R 3 , R 3 and R 4 , and R 4 and R 5 may be together combined to form a ring which may contain one or more (preferably 1 to 2) oxygen atoms, and R 6 and R 7 are the same or different, and each represents a linear or branched alkyl group having 1 to 6 carbon atoms, etc.).
    一种新型膦化合物,具有优异的性能(化学选择性、对映选择性、催化活性),作为不对称合成催化剂,特别是不对称氢化反应的催化剂。该膦-膦酰化合物由下列通式1表示:其中,R1表示氢原子或具有1至4个碳原子的线性或支链烷基;R2、R3、R4和R5相同或不同,每个表示氢原子或具有1至6个碳原子的烷基等;R2和R3、R3和R4、R4和R5中的每一对可以结合形成一个环,该环可以包含一个或多个(优选1至2个)氧原子;R6和R7相同或不同,每个表示具有1至6个碳原子的线性或支链烷基等。
  • Fatty alcohols through hydroxylation of symmetrical alkenes with selenium dioxide/<i>tert.</i>‐butylhydroperoxide
    作者:G. Knothe、M. O. Bagby、D. Weisleder
    DOI:10.1007/bf02660715
    日期:1995.9
    Abstract

    Several symmetrical alkenes were reacted with the selenium dioxide/tert.‐butylhydroperoxide system to give three hydroxylated products each. These products were those of allylic mono‐ and dihydroxylation (meso andthreo dihydroxy compounds) of the double bond. Some dihydroxy products were hydrogenated to give saturated 1,4‐diols. The compounds were characterized by nuclear magnetic resonance. The products have potential for application in commercial products, such as biodiesel, lubricants, greases, and cosmetics.

    摘要 几种对称烯与二氧硒/叔丁基过氧化氢体系反应,各得到三种羟基化产物。这些产物是双键的烯丙基一羟基化和二羟基化(中二羟基化合物和三羟基化合物)。一些二羟基产物经氢化后得到饱和的 1,4-二醇。核磁共振对这些化合物进行了表征。这些产品具有应用于生物柴油、润滑油、润滑脂和化妆品等商业产品的潜力。
  • PROCESS FOR PREPARING EPISULFIDE COMPOUNDS
    申请人:Asahi Kasei Chemicals Corporation
    公开号:EP2700636A1
    公开(公告)日:2014-02-26
    Provided is a method for producing an episulfide compound, the method including a step of thiating epoxy groups of (B) an epoxy compound by a reaction with (C) a thiating agent in the presence of (A) a polyhydric hydroxyl compound having two or more hydroxyl groups.
    本发明提供了一种生产环硫化化合物的方法,该方法包括以下步骤:在(A)具有两个或两个以上羟基的多羟基化合物存在下,通过与(C)硫化剂反应,硫化(B)环氧化合物的环氧基团。
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