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(-)-(1R,7R)-1,7-dimethylnonyl propanoate | 90410-62-1

中文名称
——
中文别名
——
英文名称
(-)-(1R,7R)-1,7-dimethylnonyl propanoate
英文别名
8r-Methyl-2r-decyl propanoate;[(2R,8R)-8-methyldecan-2-yl] propanoate
(-)-(1R,7R)-1,7-dimethylnonyl propanoate化学式
CAS
90410-62-1
化学式
C14H28O2
mdl
——
分子量
228.375
InChiKey
DHRLLFVOVDPRNS-CHWSQXEVSA-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):
    5.2
  • 重原子数:
    16
  • 可旋转键数:
    10
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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 the propionates of (2r, 8r)- and (2s, 8r)-8-methyl-2-decanol, the pheromone of the western corn rootworm, employing chiral compounds of microbial origin as starting materials
    作者:Kenji Mori、Hindenori Watanabe
    DOI:10.1016/s0040-4020(01)91175-5
    日期:1984.1
    The attractants of the western corn rootworm (Diabrotica virgiferaLe Counte), the propionates of (2R, 8R)-and (2S, 8R)-8-methyl-2-decanol, were synthesized from (R)-(+)-citronellol and the enantiomers of ethyl β-hydroxybutryate of microbial origin.
    由(R)-(+)-香茅醇合成西部玉米根虫(Diabrotica virgifera Le Counte)的引诱剂,(2R,8R)-和(2S,8R)-8-甲基-2-癸醇的丙酸酯。和微生物来源的β-羟基丁酸乙酯的对映体。
  • Hydrolytic kinetic resolution of terminal mono- and bis-epoxides in the synthesis of insect pheromones: routes to (−)-( R )- and (+)-( S )-10-methyldodecyl acetate, (−)-( R )-10-methyl-2-tridecanone, (−)-( R )-( Z )-undec-6-en-2-ol (Nostrenol), (−)-(1 R ,7 R )-1,7-dimethylnonyl propanoate, (−)-(6 R ,12 R )-6,12-dimethylpentadecan-2-one, (−)-(2 S ,11 S )-2,11-diacetoxytridecane and (+)-(2 S ,12 S )-2,12-diacetoxytridecane
    作者:Sharon Chow、William Kitching
    DOI:10.1016/s0957-4166(02)00175-1
    日期:2002.5
    enantiomerically enriched epoxides and diols, which have been transformed into important insect sex pheromones. In this general approach, (−)-(R)- and (+)-(S)-10-methyldodecyl acetates from the smaller tea tortrix moth were obtained, as was (−)-(R)-10-methyltridecan-2-one from the southern corn rootworm. The (S)-epoxide obtained from undec-1-en-6-yne was transformed to (−)-(R)-(Z)-undec-6-en-2-ol (Nostrenol)
    使用(salen)Co(OAc)配合物的官能化环氧化物的水解动力学拆分(HKR)提供了对映体富集的环氧化物和二醇,它们已转化为重要的昆虫性信息素。在这种通用方法中,从较小的茶to蛾中获得了(-)-(R)-和(+)-(S)-10-甲基十二烷基乙酸酯,以及(-)-(R)-10-甲基叔丁基酚2 -来自南部玉米根虫的一种。从十一烯-1-烯-6-炔获得的(S)-环氧化物从蚁狮转变为(-)-(R)-(Z)-十一烯-6-烯-2-醇(Nostrenol)。还研究了合适的双环氧化物的HKR,并提供了生成的双环氧化物和环氧二醇的转化(-)-(1 R,7 - [R )从玉米根-1,7- dimethylnonylpropanoate,( - ) - (6 - [R,12 - [R)-6,12-dimethylpentadecan -2-酮从阴带状黄瓜甲虫,和( - ) - (2-小号来自雌豌豆mid的,11 S
  • Asymmetric Total Synthesis of Four Stereoisomers of the Sex Pheromone of the Western Corn Rootworm
    作者:Zhi-Feng Sun、Tao Zhang、Jinyang Liu、Zhen-Ting Du、Huaiji Zheng
    DOI:10.3390/molecules23030667
    日期:——
    A convergent synthesis of four stereoisomers of the sex pheromone of the western corn rootworm (8-methyldecan-2-yl propionate, 1) from commercially available chiral starting materials is reported. The key step was Julia–Kocienski olefination between chiral BT-sulfone and chiral aldehyde. This synthetic route provided the four stereoisomers of 1 in 24–29% total yield via a six-step sequence. The simple
    报道了从市售手性起始材料合成西部玉米根虫性信息素的四种立体异构体(8-methyldecan-2-yl propionate, 1)。关键步骤是手性 BT-砜和手性醛之间的 Julia-Kocienski 烯化。该合成路线通过六步序列以 24-29% 的总产率提供了 1 的四种立体异构体。简单的放大策略为实现性信息素的不对称合成提供了一种新方法。
  • Hydrolytic kinetic resolution of mono- and bisepoxides as a key step in the synthesis of insect pheromones
    作者:Sharon Chow、William Kitching
    DOI:10.1039/b102181h
    日期:——
    The synthetic utility of the readily separated epoxides, diols, epoxydiols and tetrols of high enantiomeric excesses, obtained by hydrolytic kinetic resolution (HKR) of functionalised mono- and bisepoxides with (salen)Co(OAc) complexes, is demonstrated by their efficient transformations to important insect pheromones.
    通过使用 (salen)Co(OAc) complexes 对功能化的单环和双环环氧化物进行水解动力学分辨 (HKR) 所获得的高对映体过量的易分离环氧化物、二醇、环氧二醇和四醇的合成实用性,通过其高效转化为重要的昆虫信息素得以体现。
  • Thermostable enzymes in organic synthesis. 7. Total synthesis of the western corn rootworm sex pheromone 8-methyldec-2-yl propanoate using a TBADH-generated C2-bifunctional chiron
    作者:Ehud Keinan、Subhash C. Sinha、Anjana Sinha-Bagchi
    DOI:10.1021/jo00039a023
    日期:1992.6
    Enantiomerically pure alcohols produced by Thermoanaerobium brockii alcohol dehydrogenase (TBADH)-catalyzed asymmetric reduction of polyfunctional ketones are useful building blocks for natural products synthesis. This advantage has been demonstrated by a total synthesis of all four isomers of 8-methyldec-2-yl propanoate, the sex pheromone emitted by the female western corn rootworm, Diabrotica virgifera virgifera LeConte. These four isomers were obtained in a very short procedure (either three or five steps) with an enantiomeric purity that exceeds 99% using a single chiral building block, (2S,8S)-(+)-2,8-dihydroxynonane. The latter diol, characterized by a synthetically useful C2 symmetry, was obtained by TBADH-catalyzed reduction of nonane-2,8-dione.
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