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8-Acetoxy-2,6-dimethyl-2,6-octadien-1-ol | 43009-62-7

中文名称
——
中文别名
——
英文名称
8-Acetoxy-2,6-dimethyl-2,6-octadien-1-ol
英文别名
(8-hydroxy-3,7-dimethylocta-2,6-dienyl) acetate
8-Acetoxy-2,6-dimethyl-2,6-octadien-1-ol化学式
CAS
43009-62-7
化学式
C12H20O3
mdl
——
分子量
212.289
InChiKey
HZIJXISIZGWHAY-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):
    2.2
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.58
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

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

点击查看最新优质反应信息

文献信息

  • Electrophilic cyclization of α- and β-geranyl acetates by mercury(II) trifluoroacetate
    作者:V. N. Kulchitski、N. D. Ungur、P. F. Vlad
    DOI:10.1007/bf02495925
    日期:1997.7
    Electrophilic cyclization of β-geranyl acetate promoted by mercury(II) trifluoroacetate leads to mixtures of α- and γ-5αH-cyclogeranyl acetate derivatives and 6α-hydroxy-5αH-and 6α-hydroxy-5βH-cyclogeranyl acetate derivatives mercurated at the C-3 atom. The ratio of the unsaturated and hydroxymercurated products depends on the reaction conditions. α-Geranyl acetate reacts with mercury(II) trifluoroacetate
    由三氟乙酸汞 (II) 促进的 β-香叶基乙酸酯的亲电环化导致 α- 和 γ-5αH-环香叶基乙酸酯衍生物与 6α-羟基-5αH-和 6α-羟基-5βH-环香叶基乙酸酯衍生物的混合物在 C- 3 原子。不饱和和羟基汞化产物的比例取决于反应条件。α-香叶基乙酸酯与三氟乙酸汞 (II) 反应生成 6α-羟基-5αH-和 6α-羟基-5βH-香叶基乙酸酯的混合物,在 C-9 处汞化,在 C-4 处具有赤道亚​​甲基汞基。含汞环香叶基衍生物中的含汞基团很容易被含氧官能团还原或取代;这构成了难以获得的多官能环香叶基衍生物的便捷途径。
  • Epothilone synthesis building blocks III and IV: asymmetrically substituted acyloins and acyloin derivatives, methods for their production and methods for the production of epothilones B, D and epothilone derivatives
    申请人:——
    公开号:US20040082651A1
    公开(公告)日:2004-04-29
    The present invention is directed to novel acyloins, their derivatives, methods for their production and their use for the production of novel epothilones and their derivatives. In addition, the invention is directed to the building blocks for epothilone synthesis, methods for their production and the use of synthetic building blocks for the production of epothilones and their derivatives.
    本发明涉及新型酰亚胺、其衍生物、其生产方法以及用于生产新型依托利酮及其衍生物的方法。此外,本发明还涉及依托利酮合成的构建块、其生产方法以及用于生产依托利酮及其衍生物的合成构建块的使用。
  • Substituted-acyclic terpene compound
    申请人:Mitsubishi Kasei Corporation
    公开号:US05245085A1
    公开(公告)日:1993-09-14
    Acyclic terpene compounds useful as intermediates for producing sarcophytol A which have an anti-carcinogenic promoter activity and anti-tumor activity, which compounds are shown by the general formula (I): ##STR1##
    无环萜烯化合物可用作生产蜥蜴毒醇A的中间体,具有抗癌促进活性和抗肿瘤活性,这些化合物由通式(I)所示:## STR1 ##
  • SUBSTITUTED OPEN-CHAIN TERPENE COMPOUND
    申请人:Mitsubishi Chemical Corporation
    公开号:EP0455826A1
    公开(公告)日:1991-11-13
    A novel substituted open-chain terpene compound of general formula (I) which is useful as an intermediate for the synthesis of sarcophytol A, wherein R is (α), (β), or (ψ) (wherein R¹ is cyano or formyl R² is hydrogen or CO₂R³, R³ is C₁ to C₄ alkyl, and R⁴ is -C=CH or -CH=CH₂); X is hydrogen, hydroxyl, halogen, OR⁵ or OSO₂R⁶ (wherein R⁵ is hydrogen, 1-alkoxyalkyl, tetrahydrofuryl, tetrahydropyranyl, acyl, or silyl substituted by C₁ to C₅ alkyl or phenyl, and R⁶ is C₁ to C₄ alkyl which may be substituted by halogen or phenyl which may be substituted by C₁ to C₄ alkyl); and n is an integer of O to 2, provided that X is OR⁵ and n is O when R is (β) or (ψ); X is neither halogen nor OSO₂R⁶ when R¹ is formyl; R² is not hydrogen when R⁵ is hydrogen; and R³ is not methyl when R⁵ is 1-ethoxyethyl.
    一种通式(I)的新型取代开链萜烯化合物,可作为合成肌醇 A 的中间体,其中 R 是 (α)、(β)或 (ψ)(其中 R¹ 是氰基或甲酰基 R² 是氢或 CO₂R³,R³ 是 C₁ 至 C₄ 烷基,R⁴ 是 -C=CH 或 -CH=CH₂);X 是氢、羟基、卤素、OR⁵ 或 OSO₂R⁶(其中 R⁵ 是氢、1-烷氧基烷基、四氢糠基、四氢吡喃基、酰基或被 C₄ 烷基取代的硅烷基)、或被 C₁ 至 C₅ 烷基或苯基取代的硅烷基,而 R⁶ 是可被卤素取代的 C₁ 至 C₄ 烷基或可被 C₁ 至 C₄ 烷基取代的苯基);且 n 为 O 至 2 的整数,条件是当 R 为 (β) 或 (ψ) 时,X 为 OR⁵,且 n 为 O;当 R¹ 为甲酰基时,X 既不是卤素,也不是 OSO₂R⁶;当 R⁵ 为氢时,R² 不是氢;当 R⁵ 为 1-乙氧基乙基时,R³ 不是甲基。
  • PROCESS FOR PRODUCING OXYGENIC COMPOUND
    申请人:Sumitomo Chemical Company, Limited
    公开号:EP1797953B1
    公开(公告)日:2011-01-05
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