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2-allylbutane-1,3-diol | 89794-49-0

中文名称
——
中文别名
——
英文名称
2-allylbutane-1,3-diol
英文别名
3-Hydroxymethyl-5-hexen-2-ol;2-Prop-2-enylbutane-1,3-diol
2-allylbutane-1,3-diol化学式
CAS
89794-49-0
化学式
C7H14O2
mdl
——
分子量
130.187
InChiKey
FCMRZSJKFOBTKZ-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):
    0.7
  • 重原子数:
    9
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.71
  • 拓扑面积:
    40.5
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2-allylbutane-1,3-diol双氧水 、 sodium hydride 、 sodium hydroxide 作用下, 以 四氢呋喃甲醇N,N-二甲基甲酰胺 为溶剂, 反应 3.5h, 生成 5-((4-methoxybenzyl)oxy)-4-(((4-methoxybenzyl)oxy)methyl)hexan-1-ol
    参考文献:
    名称:
    用于合成烷基环丙烷的 1,3-二甲磺酸盐的镍催化烷基-烷基交叉电泳偶联反应
    摘要:
    两个 Csp3-X 键的交叉亲电偶联反应仍然具有挑战性。在此,我们报告了分子内镍催化的 1,3-二醇衍生物的交叉亲电偶联反应。值得注意的是,这种转化用于合成一系列单和 1,2-二取代的烷基环丙烷,包括衍生自萜烯、类固醇和醛醇产品的那些。此外,对映体富集的环丙烷是由脯氨酸催化和埃文斯羟醛反应的产物合成的。还描述了将 1,3-二醇直接转化为环丙烷的过程。计算和实验数据与镍催化机制一致,该机制始于二级中心的立体氧化加成。
    DOI:
    10.1021/jacs.0c01330
  • 作为产物:
    描述:
    2-乙酰基戊-4-烯酸甲酯 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 生成 2-allylbutane-1,3-diol
    参考文献:
    名称:
    β-羟基酯的二价阴离子Claisen重排
    摘要:
    β-羟基烯丙基酯双阴离子的Claisen重排可立体控制无环构架上三个连续手性中心的进入;已经开发出用于评估非对映选择性的明确方法。
    DOI:
    10.1016/s0040-4039(01)91102-5
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文献信息

  • Preparation of mixtures of butanediols
    申请人:E.I. DU PONT DE NEMOURS AND COMPANY
    公开号:EP0340970A2
    公开(公告)日:1989-11-08
    Process for preparing 2-alkyl-1,4-butanediols and mixtures with 1,4-butanediol which comprises bringing together, at an initial alkaline pH, and at a temperature and pressure suitable for reaction, a mixture of 4-hydroxybutyraldehyde and/or its cyclic acetal, 2-hydroxytetrahydrofuran, hydrogen, an unsubstituted aliphatic aldehyde, especially formaldehyde, and a hydrogenation catalyst. Also processes for preparing mixtures of tetrahydrofuran and 3-alkyltetrahydrofuran from the diol mixtures, and copolymers from the tetrahydrofuran mixtures.
    制备 2-烷基-1,4-丁二醇及与 1,4-丁二醇的混合物的工艺,包括在初始碱性 pH 值和适合反应的温度和压力下,将 4-羟基丁醛和/或其环状缩醛2-羟基四氢呋喃氢气、未取代脂肪醛(尤其是甲醛)和催化剂的混合物混合在一起。此外,还有从二元醇混合物中制备四氢呋喃和 3-烷基四氢呋喃混合物的工艺,以及从四氢呋喃混合物中制备共聚物的工艺。
  • CURABLE RESIN COMPOSITION AND METHOD FOR FORMING CURED COATING FILM
    申请人:Daicel Chemical Industries, Ltd.
    公开号:EP2048196A1
    公开(公告)日:2009-04-15
    Disclosed is a curable resin composition which contains a copolymer; and an organic solvent having a boiling point of 180°C or higher at atmospheric pressure, which copolymer contains monomer units (A) having an alkali-soluble group, and monomer units (B) corresponding to curable group-containing polymerizable unsaturated compounds. The copolymer contains the monomer units (B) in a content of 5 to 95 percent by weight, based on the total weight of monomer units constituting the copolymer, and the monomer units (B) contain 30 percent by weight or more of monomer units corresponding to at least one compound selected from compounds containing an 3,4-epoxytricyclo[5.2.1.02,6]decane ring. The curable resin composition gives a coat which is superior typically in transparency and thermal stability and does not suffer from uneven thickness and coating defects particularly when the composition is applied through slit coating or ink-jet coating.
    本发明公开了一种可固化树脂组合物,它含有一种共聚物;和一种在常压下沸点为 180℃或更高的有机溶剂,该共聚物含有具有碱溶性基团的单体单元(A)和与含可固化基团的可聚合不饱和化合物相对应的单体单元(B)。以构成共聚物的单体单元总重量为基准,共聚物中单体单元(B)的含量为 5%至 95%(按重量计),单体单元(B)中至少含有一种选自含有 3,4-环三环[5.2.1.02,6]癸烷环的化合物的单体单元,含量为 30%(按重量计)或更多。这种可固化树脂组合物所制成的涂层具有优异的透明度和热稳定性,不会出现厚度不均和涂层缺陷,尤其是在通过狭缝涂布或喷墨涂布的情况下。
  • ——
    作者:V. V. Kuznetsov、E. A. Alekseeva、V. V. Khudyakov、Yu. A. Levshov
    DOI:10.1023/a:1015447702040
    日期:——
    H-1 NMR spectroscopy and MM+ and AM1 calculations were used for configurational assessment of stereoisomers of 4-methyl-2,5-disubstituted 1,3,2-dioxaborinanes (differing in the configuration of the ring C-4 atom). The molecules are conformationally inhomogeneous; this is due to the internal rotation of the substituent at the C-5 atom, while in the cis isomers, in addition, by the equilibrium between the S-4e5a and S-4a5e sofa conformations, shifted to the latter form.
  • KURTH, M. J.;YU, CAN-MO, TETRAHEDRON LETT., 1984, 25, N 44, 5003-5006
    作者:KURTH, M. J.、YU, CAN-MO
    DOI:——
    日期:——
  • COMPOUNDS THAT INHIBIT MCL-1 PROTEIN
    申请人:AMGEN INC.
    公开号:US20210230189A1
    公开(公告)日:2021-07-29
    Provided herein are myeloid cell leukemia 1 protein (Mcl-1) inhibitors, methods of their preparation, related pharmaceutical compositions, and methods of using the same. For example, provided herein are compounds of Formula I, and pharmaceutically acceptable salts thereof and pharmaceutical compositions containing the compounds. The compounds and compositions provided herein may be used, for example, in the treatment of diseases or conditions, such as cancer.
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