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6-oxo-1-nonanol | 4066-93-7

中文名称
——
中文别名
——
英文名称
6-oxo-1-nonanol
英文别名
9-hydroxynonan-4-one;6-oxononan-1-ol;1-hydroxy-6-nonanone;6-oxo-Nonan-1-ol
6-oxo-1-nonanol化学式
CAS
4066-93-7
化学式
C9H18O2
mdl
——
分子量
158.241
InChiKey
AGSKJBKUKWUEEU-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):
    1.1
  • 重原子数:
    11
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 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

  • 作为反应物:
    参考文献:
    名称:
    PERKINS, M. V.;FLETCHER, M. T.;KITCHING, W.;DREW, R. A. I.;MOORE, C. J., J. CHEM. ECOL., 16,(1990) N, C. 2475-2587
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    OSHEA, MICHAEL G.;KITCHING, WILLIAM, TETRAHEDRON, 45,(1989) N, C. 1177-1186
    摘要:
    DOI:
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文献信息

  • Wacker-Type Oxidation of Internal Olefins Using a PdCl2/N,N-Dimethylacetamide Catalyst System under Copper-Free Reaction Conditions
    作者:Takato Mitsudome、Keiichi Mizumoto、Tomoo Mizugaki、Koichiro Jitsukawa、Kiyotomi Kaneda
    DOI:10.1002/anie.200905184
    日期:——
    A simple catalyst system consisting of PdCl2 and N,N‐dimethylacetamide (DMA) as the solvent can successfully promote Wacker‐type oxidation of internal olefins. This catalyst system does not require copper compounds and is tolerant of a wide range of substrates having internal olefins.
    由PdCl 2和N,N-二甲基乙酰胺(DMA)作为溶剂组成的简单催化剂体系可以成功地促进内烯烃的Wacker型氧化。该催化剂体系不需要化合物,并且可以耐受多种具有内烯烃的底物。
  • Visible-Light-Promoted Catalytic Ring-Opening Isomerization of 1,2-Disubstituted Cyclopropanols to Linear Ketones
    作者:Marharyta V. Laktsevich-Iskryk、Nastassia A. Varabyeva、Volha V. Kazlova、Vladimir N. Zhabinskii、Vladimir A. Khripach、Alaksiej L. Hurski
    DOI:10.1002/ejoc.202000094
    日期:2020.5.3
    A visible‐light‐promoted acridinium‐catalyzed radical isomerization of 1,2‐disubstituted cyclopropoanols to linear ketones is reported.
    据报道1,2-二取代的环丙醇在可见光促进下的din啶催化的自由基异构化为线性酮。
  • Electrophysiological Responses of Bactrocera kraussi (Hardy) (Tephritidae) to Rectal Gland Secretions and Headspace Volatiles Emitted by Conspecific Males and Females
    作者:Sally Noushini、Soo Jean Park、Jeanneth Perez、Danielle Holgate、Vivian Mendez、Ian M. Jamie、Joanne F. Jamie、Phillip W. Taylor
    DOI:10.3390/molecules26165024
    日期:——
    Pheromones are biologically important in fruit fly mating systems, and also have potential applications as attractants or mating disrupters for pest management. Bactrocera kraussi (Hardy) (Diptera: Tephritidae) is a polyphagous pest fruit fly for which the chemical profile of rectal glands is available for males but not for females. There have been no studies of the volatile emissions of either sex
    信息素在果蝇交配系统中具有重要的生物学意义,并且还具有作为害虫管理的引诱剂或交配干扰剂的潜在应用。 Bactrocera kraussi (Hardy)(双翅目:实蝇科)是一种杂食性害虫果蝇,其直肠腺的化学特征仅适用于雄性,但不适用于雌性。目前还没有关于性别挥发性排放或对这些化合物的电生理反应的研究。本研究(i)通过气相色谱-质谱(GC-MS)建立了两性B. kraussi直肠腺内容物和挥发物的化学特征,(ii)评估了气相色谱对已鉴定化合物的检测 -触角电图检测(GC-EAD)和触角电图检测(GC-EPD)。在雄性B. kraussi 的直肠腺中鉴定出 16 种化合物,在雌性 B. kraussi的直肠腺中鉴定出 29 种化合物。在这些化合物中,有 5 种在雄性的顶部空间中检测到,13 种在雌性的顶部空间中检测到。 GC-EPD 测定记录了两性针对 ( E , E )-2,8-二甲基-1,7-二氧螺[5
  • [EN] CARBOSTYRIL COMPOUND<br/>[FR] DÉRIVÉ DE CARBOSTYRILE
    申请人:OTSUKA PHARMA CO LTD
    公开号:WO2006035954A1
    公开(公告)日:2006-04-06
    The present invention provides a carbostyril compound represented by General Formula (1) or a salt thereof, wherein A is a direct bond, a lower alkylene group, or a lower alkylidene group; X is an oxygen atom or a sulfur atom; R4 and R5 each represent a hydrogen atom; the bond between the 3 and 4 positions of the carbostyril skeleton is a single bond or a double bond; R1 is a hydrogen atom, etc; R2 is a hydrogen atom, etc; and R3 is a hydrogen atom, etc. The carbostyril compound or salt thereof of the present invention induces the production of TFF, and thus is usable for the treatment and/or prevention of disorders such as alimentary tract diseases, oral diseases, upper respiratory tract diseases, respiratory tract diseases, eye diseases, cancers, and wounds.
    本发明提供了一种由通式(1)表示的羧基吲哚化合物或其盐,其中A是直链键、较低的烷基烯基或较低的烷基亚烯基;X是氧原子或原子;R4和R5分别表示氢原子;羧基吲哚骨架的3和4位置之间的键是单键或双键;R1是氢原子,等等;R2是氢原子,等等;R3是氢原子,等等。本发明的羧基吲哚化合物或其盐诱导TFF的产生,因此可用于治疗和/或预防消化道疾病、口腔疾病、上呼吸道疾病、呼吸道疾病、眼部疾病、癌症和伤口等疾病。
  • METHOD FOR MANUFACTURING KETONE
    申请人:Kaneda Kiyotomi
    公开号:US20120197036A1
    公开(公告)日:2012-08-02
    A method for manufacturing a ketone, includes oxidizing an internal olefin or a cyclic olefin having a functional group containing a hetero atom and one carbon-carbon double bond or more at a position other than terminals of a molecule thereof in an amide-based solvent in the presence of water, a palladium catalyst, and molecular oxygen, without oxidizing the functional group, thereby bonding an oxo group to at least one of the carbon atoms constituting the carbon-carbon double bond. The amide-based solvent is represented by formula (1): wherein R 1 represents an alkyl group having 1 to 4 carbon atoms; R 2 and R 3 each independently represent an alkyl group having 1 to 4 carbon atoms or an aryl group; and when R 1 and R 2 are alkyl groups, R 1 and R 2 may be bonded to each other to form a ring structure.
    一种制备酮的方法,包括在酰胺基溶剂中,在催化剂和分子氧的存在下氧化具有异原子和一个或多个碳碳双键的内部烯烃或环烯烃,其功能团位于分子的端部以外的位置,而不氧化功能团,从而将氧代基键合到构成碳碳双键的至少一个碳原子上。酰胺基溶剂由式(1)表示:其中R1代表具有1至4个碳原子的烷基基团;R2和R3各自独立地代表具有1至4个碳原子的烷基基团或芳基;当R1和R2为烷基基团时,R1和R2可以结合在一起形成环结构。
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