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2-methyl-3-isopropylheptane-3-ol | 5340-35-2

中文名称
——
中文别名
——
英文名称
2-methyl-3-isopropylheptane-3-ol
英文别名
2-methyl-3-isopropyl-3-heptanol;3-methyl-3-(2'-propyl)-3-heptanol;n-Butyl-diisopropylcarbinol;3-isopropyl-2-methyl-heptan-3-ol;Diisopropyl-butyl-carbinol;2-Methyl-3-(propan-2-yl)heptan-3-ol;2-methyl-3-propan-2-ylheptan-3-ol
2-methyl-3-isopropylheptane-3-ol化学式
CAS
5340-35-2
化学式
C11H24O
mdl
——
分子量
172.311
InChiKey
JEVTXHCZDDBPDA-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

  • 沸点:
    115-118 °C(Press: 45 Torr)
  • 密度:
    0.8487 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:3af49de59890c8fc44bff04c3f1b7d28
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反应信息

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文献信息

  • Impact of reaction products on the Grignard reaction with silanes and ketones
    作者:Dmitri Panov、Ants Tuulmets、Binh T. Nguyen
    DOI:10.1016/j.jorganchem.2006.06.012
    日期:2006.9
    Grignard reactions with alkoxysilanes or carbonyl compounds produce alkoxymagnesium halides as by-products. Kinetic measurements for reactions of silanes and of a ketone were performed with Grignard reagents, enriched in alkoxymagnesium halides and taken in a great excess.
    与烷氧基硅烷或羰基化合物的格氏反应产生副产物烷氧基镁卤化物。用格氏试剂对硅烷和酮的反应进行动力学测量,该试剂富含烷氧基镁卤化物,并且过量使用。
  • Tertiäre, alkylsubstituierte Alkohole als Riechstoffe
    申请人:Henkel Kommanditgesellschaft auf Aktien
    公开号:EP0237980A2
    公开(公告)日:1987-09-23
    Die Erfindung beschreibt die Verwendung tertiärer, alkylsubstituierter Alkohole der allgemeinen Formel worin die Reste R1 und R2 eine Alkylgruppe mit 1 bis 3 Kohlenstoffatomen und der Rest R3 eine Alkylgruppe mit 4 bis 9 Kohlenstoffatomen bedeuten, als Riechstoffe in aktivchlorhaltigen Mischungen.
    本发明描述了通式为叔烷基取代醇的用途,通式中的自由基 R1 和 R2 表示具有 1 至 3 个碳原子的烷基,自由基 R3 表示具有 4 至 9 个碳原子的烷基。
  • Samarium(II) Triflate as a New Reagent for the Grignard-Type Carbonyl Addition Reaction
    作者:Shin-ichi Fukuzawa、Keisuke Mutoh、Teruhisa Tsuchimoto、Tamejiro Hiyama
    DOI:10.1021/jo960260s
    日期:1996.1.1
    On treatment of a THF solution of Sm(OTf)(3) with 1 equiv of an organolithium or organomagnesium reagent-at ambient temperature, the purple or deep green solution of the divalent samarium triflate [Sm(OTf)(2)] was readily obtained. For this preparation, s-BuLi was the most effective as was evidenced by the reduction of a-phenylethyl iodide in the presence of HMPA. The Sm(OTf)(2) reagent mediated the Grignard-type reaction effectively in THF/HMPA; alkylation and allylation of ketones or aldehydes with alkyl, allyl, or benzyl halides proceeded via organosamarium intermediates. Diastereoselectivity of the samarium-Grignard reaction was examined using 2-methylcyclohexanone, 4-tert-butylcyclohexanone, and 2-phenylpropanal and was found to be higher in each case than that with SmI2. With 2-methylcyclohexanone, for example, Sm(OTf)(2) gave the greatest ratio of axial alcohol:equatorial alcohol = 99:1, and SmI2 gave a ratio of 91:9. Halides containing an ester or a silyl group were reactive in the Reformatsky- or Peterson-type reaction, respectively, using the Sm(OTf)(2) reagent.
  • Conant; Blatt, Journal of the American Chemical Society, 1929, vol. 51, p. 1233
    作者:Conant、Blatt
    DOI:——
    日期:——
  • Denise,B. et al., Bulletin de la Societe Chimique de France, 1972, p. 990 - 1000
    作者:Denise,B. et al.
    DOI:——
    日期:——
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