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(4E,6E)-nona-4,6-dien-3-one | 118893-62-2

中文名称
——
中文别名
——
英文名称
(4E,6E)-nona-4,6-dien-3-one
英文别名
——
(4E,6E)-nona-4,6-dien-3-one化学式
CAS
118893-62-2
化学式
C9H14O
mdl
——
分子量
138.21
InChiKey
QXBIQFBTZVWQNR-BSWSSELBSA-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:
    215.0±9.0 °C(Predicted)
  • 密度:
    0.856±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

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

  • A novel stereoselective synthesis of conjugated dienones
    作者:Dawei Ma、Yingrui Lin、Xiyan Lu、Yihua Yu
    DOI:10.1016/0040-4039(88)85331-0
    日期:1988.1
    (E,E)-α,β,-γ,δ-Dienones are synthesized stereoselectively from the corresponding α,β-ynones in high yield under the catalysis of a ruthenium hydride complex.
    (E,E)-α,β,-γ,δ-二烯酮是在氢化配合物的催化下,由相应的α,β-炔酮高选择性地立体合成的。
  • PARA-QUINOL DERIVATIVES AND METHODS OF STEREO SELECTIVELY SYNTHESIZING AND USING SAME
    申请人:Plourde Guy L.
    公开号:US20090318548A1
    公开(公告)日:2009-12-24
    This application relates to para-quinol derivatives, such as analogues of manumycins, aranorosins and gymnastatins. This application also relates to methods of synthesizing and using the para-quinol derivatives. In one embodiment of the invention a compound having the chemical structure (I) is provided wherein X 1 and X 2 are carbon atoms either joined by double bond or joined by a single bond and comprising constituents of an epoxide ring or a hydroxyethylene moiety; X 3 and X 4 are carbon atoms either joined by double bond or joined by a single bond and comprising constituents of an epoxide ring; R 1 is selected from the group consisting of branched alkyl chains, unbranched alkyl chains, cycloalkyl groups, aromatic groups, alcohols, ethers, amines, and substituted or unsubstituted ureas, esters, aldehydes and carboxylic acids; and R 2 is selected from the group consisting of H, OH and NHR 3 wherein R 3 is a nitrogen protecting group. In a particular embodiment of the invention R 1 is a polyunsaturated carbon chain as found in biologically active manumycins. The applicant's synthetic method may involve diasteroselective formation of a spirolactone in an oxidative spiroannulation process using tyrosine or a tyrosine derivative having a chiral centre as a starting material.
    本申请涉及对位喹啉生物,例如曼纽霉素、阿拉诺罗辛和体操霉素的类似物。本申请还涉及合成和使用对位喹啉生物的方法。在发明的一个实施例中,提供了具有化学结构(I)的化合物,其中X1和X2是由双键连接或单键连接的碳原子,并包括环氧环或羟基乙烯基的组分;X3和X4是由双键连接或单键连接的碳原子,并包括环氧环的组分;R1选自支链烷基链,直链烷基链,环烷基团,芳香族团,醇,醚,胺和取代或未取代的、酯、醛和羧酸;R2选自H,OH和NHR3,其中R3是氮保护基。在发明的一个特定实施例中,R1是生物活性曼纽霉素中发现的多不饱和碳链。申请人的合成方法可能涉及使用酪氨酸或手性中心的酪氨酸生物作为起始材料,在氧化螺环化过程中二面体选择性地形成螺内酯
  • OLIGONUCLEOTIDES AND ANALOGS LABELED WITH ENERGY TRANSFER DYES
    申请人:Lee Linda G.
    公开号:US20100029923A1
    公开(公告)日:2010-02-04
    Novel linkers for linking a donor dye to an acceptor dye in an energy transfer fluorescent dye are provided. These linkers facilitate the efficient transfer of energy between a donor and acceptor dye in an energy transfer dye. One of these linkers for linking a donor dye to an acceptor dye in an energy transfer fluorescent dye has the general structure R 21 Z 1 C(O)R 22 R 28 where R 21 is a C 1-5 alkyl attached to the donor dye, C(O) is a carbonyl group, Z 1 is either NH, sulfur or oxygen, R 22 is a substituent which includes an alkene, diene, alkyne, a five and six membered ring having at least one unsaturated bond or a fused ring structure which is attached to the carbonyl carbon, and R 28 includes a functional group which attaches the linker to the acceptor dye.
  • US7825237B2
    申请人:——
    公开号:US7825237B2
    公开(公告)日:2010-11-02
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