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7-甲氧基-3,7-二甲基-辛-2-烯-1-醛 | 71385-05-2

中文名称
7-甲氧基-3,7-二甲基-辛-2-烯-1-醛
中文别名
——
英文名称
7-methoxy-3,7-dimethyl-octa-2-en-1-al
英文别名
3,7-dimethyl-7-methoxy-2-octenal;7-methoxy-3,7-dimethyl-oct-2-en-1-al;(E)-7-methoxy-3,7-dimethyl-oct-2-enal;7-methoxy-6,7-dihydro-geranial;3,7-dimethyl-7-methoxy-oct-2-en-1-al;(E)-7-methoxy-3,7-dimethyloct-2-enal
7-甲氧基-3,7-二甲基-辛-2-烯-1-醛化学式
CAS
71385-05-2
化学式
C11H20O2
mdl
——
分子量
184.279
InChiKey
AMLBMXAXWXKAFL-JXMROGBWSA-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:
    100 °C(Press: 12 Torr)
  • 密度:
    0.889±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    13
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.73
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:0cc9c3779c15988915078333975ce0ea
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反应信息

  • 作为产物:
    描述:
    7-甲氧基-3,7-二甲基-2-辛烯-1-醇 在 manganese(IV) oxide 作用下, 以 Petroleum ether 为溶剂, 生成 7-甲氧基-3,7-二甲基-辛-2-烯-1-醛
    参考文献:
    名称:
    Patwardhan,S.A.; Gupta,A.S., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1979, vol. 17, p. 76 - 78
    摘要:
    DOI:
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文献信息

  • CATALYST FOR ASYMMETRIC HYDROGENATION AND METHOD FOR MANUFACTURING OPTICALLY ACTIVE CARBONYL COMPOUND USING THE SAME
    申请人:YAMADA Shinya
    公开号:US20120136176A1
    公开(公告)日:2012-05-31
    The present invention provides a catalyst used for manufacturing an optically active carbonyl compound by selective asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, which is insoluble in a reaction mixture, and a method for manufacturing the corresponding optically active carbonyl compound. Particularly, the invention provides a catalyst for obtaining an optically active citronellal useful as a flavor or fragrance, by selective asymmetric hydrogenation of citral, geranial or neral. The invention relates to a catalyst for asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, which comprises: a powder of at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table, or a metal-supported substance in which the at least one metal is supported on a support; an optically active peptide compound; and an acid, and also relates to a method for manufacturing an optically active carbonyl compound using the same.
    本发明提供了一种用于通过选择性不对称加氢α,β-不饱和羰基化合物制备光学活性羰基化合物的催化剂,该催化剂在反应混合物中不溶解,并提供了制备相应光学活性羰基化合物的方法。特别地,该发明提供了一种催化剂,通过选择性不对称加氢柠檬醛、香叶醛或柠檬醛制备出用作香料或芳香剂的光学活性香茅醛。该发明涉及一种用于不对称加氢α,β-不饱和羰基化合物的催化剂,包括:来自周期表第8至第10族金属中至少一种金属的粉末,或者至少一种金属负载物质,其中至少一种金属负载在一种载体上;一种光学活性肽化合物;和一种酸,还涉及使用该催化剂制备光学活性羰基化合物的方法。
  • CATALYST FOR ASYMMETRIC HYDROGENATION
    申请人:MAEDA Hironori
    公开号:US20100324338A1
    公开(公告)日:2010-12-23
    This invention aims at providing a catalyst for producing an optically active aldehyde or an optically active ketone, which is an optically active carbonyl compound, by carrying out selective asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, particularly a catalyst which is insoluble in a reaction mixture for obtaining optically active citronellal which is useful as a flavor or fragrance, by carrying out selective asymmetric hydrogenation of citral, geranial or neral; and a method for producing a corresponding optically active carbonyl compound. The invention relates to a catalyst for asymmetric hydrogenation of an α,β-unsaturated carbonyl compound, which comprises a powder of at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table, or a metal-supported substance in which at least one metal selected from metals belonging to Group 8 to Group 10 of the Periodic Table is supported on a support, an optically active cyclic nitrogen-containing compound and an acid.
    这项发明旨在通过对α,β-不饱和羰基化合物进行选择性不对称加氢,特别是通过对柠檬醛、香叶醛或柠檬醛进行选择性不对称加氢,从而提供用作香料或香精的有用的光学活性香茅醛的催化剂,该香茅醛是一种光学活性羰基化合物;以及生产相应的光学活性羰基化合物的方法。该发明涉及一种用于不对称加氢α,β-不饱和羰基化合物的催化剂,其包括来自周期表第8至第10族金属中至少一种金属的粉末,或者至少一种来自周期表第8至第10族金属的金属负载物质,该金属负载在一种支撑物上,还包括光学活性的含氮环化合物和酸。
  • Gavrilyuk, O. A.; Korchagina, D. V.; Osadchii, S. A., Journal of Organic Chemistry USSR (English Translation), 1988, vol. 24, p. 871 - 885
    作者:Gavrilyuk, O. A.、Korchagina, D. V.、Osadchii, S. A.、Barkhash, V. A.
    DOI:——
    日期:——
  • Erman, M. B.; Golovacheva, E. V.; Gulyi, S. E., Journal of Organic Chemistry USSR (English Translation), 1990, vol. 26, # 2.1, p. 219 - 221
    作者:Erman, M. B.、Golovacheva, E. V.、Gulyi, S. E.、Zasetskii, D. L.、Shutikova, L. A.、et al.
    DOI:——
    日期:——
  • EHRMAN, M. B.;GOLOVACHEVA, E. V.;GULYJ, S. E.;ZASETSKIJ, D. L.;SHUTIKOVA,+, ZH. ORGAN. XIMII, 26,(1990) N, S. 262-265
    作者:EHRMAN, M. B.、GOLOVACHEVA, E. V.、GULYJ, S. E.、ZASETSKIJ, D. L.、SHUTIKOVA,+
    DOI:——
    日期:——
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