摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

(S)-(+)-5,5-dimethoxy-3-methyl-1-pentanol | 82538-52-1

中文名称
——
中文别名
——
英文名称
(S)-(+)-5,5-dimethoxy-3-methyl-1-pentanol
英文别名
(3S)-5,5-dimethoxy-3-methylpentan-1-ol;(S)-5,5-dimethoxy-3-methylpentan-1-ol
(S)-(+)-5,5-dimethoxy-3-methyl-1-pentanol化学式
CAS
82538-52-1
化学式
C8H18O3
mdl
——
分子量
162.229
InChiKey
HBDCUFWTLDSLAO-ZETCQYMHSA-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:
    212.8±30.0 °C(Predicted)
  • 密度:
    0.945±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    11
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    38.7
  • 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

  • Synthesis of (3S,6RS)- and (3RS,6RS)-Analogs of Component AI of the Aonidiella aurantii Sex Pheromone by Stepwise Alkylation of Acetoacetic Ester
    作者:G. Yu. Ishmuratov、R. Ya. Kharisov、M. P. Yakovleva、A. V. Galyautdinova、R. R. Gazetdinov、R. R. Muslukhov、G. A. Tolstikov
    DOI:10.1007/s10600-006-0018-5
    日期:2005.11
    Synthetic approaches to (±)- and (3S)-analogs of the AI component of the Aonidiella aurantii sex pheromone (3S)-methyl-6R-isopropenyldec-9-en-1-ylacetate based on stepwise alkylation of acetoacetic ester by 3-butenylbromide and 1,5-bifunctional 3-methylpentanes were investigated.
    基于乙酰乙酸酯通过 3- 逐步烷基化的 Aonidiella aurantii 性信息素 (3S)-methyl-6R-isopropenyldec-9-en-1-ylacetate 的 (±)- 和 (3S)- 类似物的合成方法研究了丁烯基溴和 1,5-双功能 3-甲基戊烷。
  • ——
    作者:R. Ya. Kharisov、R. R. Gazetdinov、G. Yu. Ishmuratov、G. A. Tolstikov
    DOI:10.1023/a:1012326819080
    日期:——
    The versatile chiral synthon methyl (R)-5,5-dimethoxy-3-methylpentanoate has been prepared for the first time via ozonolytic decyclization of (R)-4-menthenone, which is available from L-(-)-menthol. The optically pure juvenoid (S)-(+)-hydroprene can be prepared from the synthon.
  • (4R,6R)-6-(hydroxymethyl)-4-methyltetrahydro-2H-pyran-2-one in the synthesis of polyfunctional compounds with the methyl-branched carbon skeleton
    作者:I. V. Mineeva
    DOI:10.1134/s1070428013020127
    日期:2013.2
    A simple and efficient asymmetrical synthesis was performed of a convenient bifunctional building block, methyl (R)-5,5-dimethoxy-3-methylpentanoate and its (S)-enantiomer. The possibility was shown of its application to the synthesis of insect pheromones.
  • Synthesis of optically active forms of (E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the pheromone of the yellow scale
    作者:Kenji Mori、Shigefumi Kuwahara
    DOI:10.1016/0040-4020(82)80096-3
    日期:1982.1
    Highly optically pure enantiomers of (E)-6-isopropyl-3,9-dimethyl-5,8-decadienyl acetate, the sex pheromone of the yellow scale (Aniodiella citrina), were stereoselectively from synthesized from(R)-(+)-citronellic acid. Only the (s)-enantiomer was bioactive.
    (E)-6-异丙基-3,9-二甲基-5,8-癸二烯基乙酸酯的高旋光纯对映体,黄色鳞片性信息素(柠檬黄),是由(R)-(+)合成的-香茅酸。仅(s)-对映异构体具有生物活性。
  • Uematsu, Tamon; Umemura, Takeaki; Mori, Kenji, Agricultural and Biological Chemistry, 1983, vol. 47, # 3, p. 597 - 602
    作者:Uematsu, Tamon、Umemura, Takeaki、Mori, Kenji
    DOI:——
    日期:——
查看更多