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(+/-)-1-nonene-4-thiol | 1006684-28-1

中文名称
——
中文别名
——
英文名称
(+/-)-1-nonene-4-thiol
英文别名
Non-1-ene-4-thiol;non-1-ene-4-thiol
(+/-)-1-nonene-4-thiol化学式
CAS
1006684-28-1
化学式
C9H18S
mdl
——
分子量
158.308
InChiKey
UQNRBXXFINLTKJ-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):
    4
  • 重原子数:
    10
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.78
  • 拓扑面积:
    1
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    (+/-)-1-nonene-4-thiol正己醛 在 Et4NF*5HF 作用下, 反应 1.5h, 生成 cis-4-fluoro-2,6-dipentylthiacyclohexane
    参考文献:
    名称:
    离子液体氟化氢盐中的 Prins 环化:4-氟化四氢吡喃、硫代环己烷和哌啶的简便高效合成
    摘要:
    在离子液体氟化氢 (HF) 盐中研究了高烯丙醇与各种醛的 Prins 环化,该盐起到反应介质、催化剂和氟源的作用。该反应以优异的收率和高立体选择性(仅顺式形式)提供了相应的 4-氟化四氢吡喃。当使用在对位具有强给电子基团的苯甲醛时,该体系失去了立体选择性。为了将此方法应用于其他4-氟化杂环化合物的合成,我们还在HF盐中进行了thia-Prins和aza-Prins环化,分别成功地获得了4-氟化硫杂环己烷和哌啶。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
    DOI:
    10.1002/ejoc.200800872
  • 作为产物:
    描述:
    (+/-)-S-(1-pentyl-3-butenyl) ethanethioate 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 以76%的产率得到(+/-)-1-nonene-4-thiol
    参考文献:
    名称:
    红灯笼椒(辣椒)的同时蒸馏萃取提取物中的新的挥发性挥发性含硫成分。
    摘要:
    通过同时蒸馏-萃取(SDE,Likens-Nickerson)制备红甜椒(Capsicum annuum)的提取物。除了已知的(3 E)-3-庚-2-酮(1)外,不饱和C9-酮1-壬烯-4-酮(2),(2 E)-2-壬烯-4-酮(3)和(2 E,5 E)-2,5-nonadien-4-one(4),2-甲氧基-3-异丁基吡嗪(5)和庚烷-2-硫醇(6),我们确定了19新硫醇(脂族饱和和不饱和硫醇14-16和22-27,巯基酮12和13,巯基醇17、18和30,二硫醇19和28,甲硫醇20和21 ,以及噻吩-硫醇31)和两个新的二噻吩10和29。它们在结构上均与不饱和C7-和C9-酮1-4相关。使用Affi-Gel 501(对氨基苯酚)富集了游离硫醇-乙酸汞接枝在琼脂糖凝胶上)。
    DOI:
    10.1021/jf072493y
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文献信息

  • AMPHIPHILIC POLYMER AND PROCESSES OF FORMING THE SAME
    申请人:Janczewski Dominik
    公开号:US20100298504A1
    公开(公告)日:2010-11-25
    Disclosed are an amphiphilic polymer, its synthesis and uses thereof. The polymer has a hydrocarbon backbone with —COOH side groups. It further has first aliphatic moieties with a main chain of about 3 to about 20 carbon atoms and 0 to about 3 heteroatoms, and second aliphatic moieties that have a main chain of about 3 to about 80 carbon atoms and about 2 to about 40 heteroatoms. The second aliphatic moieties have a copolymerisable group. In the synthesis a maleic anhydride polymer of formula (I) where n is an integer from about 10 to about 10000 and R1 is H or methyl, is reacted with a monofunctional compound with an alkyl chain of about 3 to about 20 carbon atoms and 0 to about 2 heteroatoms, and with an at least bifunctional compound with an alkyl chain of about 3 to about 80 carbon atoms and 0 to about 40 heteroatoms. The functional group of the monofunctional compound and one functional group of the at least bifunctional compound can form a linkage with an anhydride. Another functional group of the at least bifunctional compound, which is not allowed to react with the maleic anhydride polymer, is copolymerisable.
  • [EN] AMPHIPHILIC POLYMER AND PROCESSES OF FORMING THE SAME<br/>[FR] POLYMÈRE AMPHIPHILE ET SES PROCÉDÉS DE FABRICATION
    申请人:AGENCY SCIENCE TECH & RES
    公开号:WO2009038544A1
    公开(公告)日:2009-03-26
    Disclosed are an amphiphilic polymer, its synthesis and uses thereof. The polymer has a hydrocarbon backbone with -COOH side groups. It further has first aliphatic moieties with a main chain of about 3 to about 20 carbon atoms and 0 to about 3 heteroatoms, and second aliphatic moieties that have a main chain of about 3 to about 80 carbon atoms and about 2 to about 40 heteroatoms. The second aliphatic moieties have a copolymerisable group. In the synthesis a maleic anhydride polymer of formula (I) where n is an integer from about 10 to about 10000 and R1 is H or methyl, is reacted with a monofunctional compound with an alkyl chain of about 3 to about 20 carbon atoms and 0 to about 2 heteroatoms, and with an at least bifunctional compound with an alkyl chain of about 3 to about 80 carbon atoms and 0 to about 40 heteroatoms. The functional group of the monofunctional compound and one functional group of the at least bifunctional compound can form a linkage with an anhydride. Another functional group of the at least bifunctional compound, which is not allowed to react with the maleic anhydride polymer, is copolymerisable.
  • New Volatile Sulfur-Containing Constituents in a Simultaneous Distillation−Extraction Extract of Red Bell Peppers (Capsicum annuum)
    作者:Regula Naef、Alain Velluz、Alain Jaquier
    DOI:10.1021/jf072493y
    日期:2008.1.1
    mercapto-alcohols 17, 18, and 30, the dithiols 19 and 28, the methylthio-thiols 20 and 21, and the thiophene-thiol 31) and the two new dithiolanes 10 and 29. All of them are structurally related to the unsaturated C7- and C9-ketones 1- 4. The free thiols were enriched using Affi-Gel 501 ( p-aminophenyl-mercuric acetate grafted on an agarose gel). The new compounds were confirmed by syntheses and were organoleptically
    通过同时蒸馏-萃取(SDE,Likens-Nickerson)制备红甜椒(Capsicum annuum)的提取物。除了已知的(3 E)-3-庚-2-酮(1)外,不饱和C9-酮1-壬烯-4-酮(2),(2 E)-2-壬烯-4-酮(3)和(2 E,5 E)-2,5-nonadien-4-one(4),2-甲氧基-3-异丁基吡嗪(5)和庚烷-2-硫醇(6),我们确定了19新硫醇(脂族饱和和不饱和硫醇14-16和22-27,巯基酮12和13,巯基醇17、18和30,二硫醇19和28,甲硫醇20和21 ,以及噻吩-硫醇31)和两个新的二噻吩10和29。它们在结构上均与不饱和C7-和C9-酮1-4相关。使用Affi-Gel 501(对氨基苯酚)富集了游离硫醇-乙酸汞接枝在琼脂糖凝胶上)。
  • Prins Cyclization in Ionic Liquid Hydrogen Fluoride Salts: Facile and Highly Efficient Synthesis of 4-Fluorinated Tetrahydropyrans, Thiacyclohexanes, and Piperidines
    作者:Yuichiro Kishi、Shinsuke Inagi、Toshio Fuchigami
    DOI:10.1002/ejoc.200800872
    日期:——
    Prins cyclization of homoallylic alcohols with various aldehydes was investigated in ionic liquid hydrogen fluoride (HF) salts, which played roles as a reaction medium, a catalyst, and a fluorine source. The reaction afforded the corresponding 4-fluorinated tetrahydropyrans in excellent yields with a high stereoselectivity (cis form exclusively). When benzaldehydes having a strongly electron-donating
    在离子液体氟化氢 (HF) 盐中研究了高烯丙醇与各种醛的 Prins 环化,该盐起到反应介质、催化剂和氟源的作用。该反应以优异的收率和高立体选择性(仅顺式形式)提供了相应的 4-氟化四氢吡喃。当使用在对位具有强给电子基团的苯甲醛时,该体系失去了立体选择性。为了将此方法应用于其他4-氟化杂环化合物的合成,我们还在HF盐中进行了thia-Prins和aza-Prins环化,分别成功地获得了4-氟化硫杂环己烷和哌啶。(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2009)
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