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2,3-二氢-9,10-二羟基-1,4-蒽二酮 | 17648-03-2

中文名称
2,3-二氢-9,10-二羟基-1,4-蒽二酮
中文别名
2,3-二氢-9,10-二羟-1,4-蒽二酮;醌茜隐色体;2,3-二氢-9,1-二羟-1,4-蒽二酮
英文名称
9,10-Dihydroxy-2,3-dihydro-anthracene-1,4-dione
英文别名
1,4-Anthracenedione, 2,3-dihydro-9,10-dihydroxy-;9,10-dihydroxy-2,3-dihydroanthracene-1,4-dione
2,3-二氢-9,10-二羟基-1,4-蒽二酮化学式
CAS
17648-03-2
化学式
C14H10O4
mdl
MFCD00012251
分子量
242.231
InChiKey
FVXPBEUYCCZFJT-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

物化性质

  • 熔点:
    154-157 °C(lit.)
  • 沸点:
    575.8±50.0 °C(Predicted)
  • 密度:
    1.511±0.06 g/cm3(Predicted)
  • 稳定性/保质期:
    按规定使用不会分解,避免与氧化剂和碱接触。

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    18
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    74.6
  • 氢给体数:
    2
  • 氢受体数:
    4

安全信息

  • 危险品标志:
    Xi
  • 安全说明:
    S24/25,S26
  • 危险类别码:
    R36/37/38
  • 海关编码:
    2914690090
  • 储存条件:
    存放于密闭、阴凉、干燥处

SDS

SDS:b53daf6c505acf272aac0b2eb16734c4
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

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文献信息

  • A new kind of H-acid monoazo-anthraquinone reactive dyes with surprising colour
    作者:Bin Shan、Xing Tong、Wei Xiong、Wenzhu Qiu、Bingtao Tang、Rongwen Lu、Wei Ma、Yi Luo、Shufen Zhang
    DOI:10.1016/j.dyepig.2015.07.001
    日期:2015.12
    were a kind of blue dyes. 1H NMR and 13C NMR results revealed that there were two kinds of tautomerisms in dye structure and a new conjugated system formed between the anthraquinone ring and the phenyl azo linkage. Density functional theory (DFT) calculations also proved the formation of the new larger conjugated system from which the blue colour was generated. The fixations of the dyes on cotton were
    以1,4-双((4-氨基苯基)氨基)蒽-9,10-二酮为重氮组分和1-氨基-8-萘酚-3为原料,得到了一种新型的同时含有单偶氮和蒽醌发色团的活性染料,以6-二磺酸(H-酸)衍生物为偶合组分。通过UV-Vis,IR,MS,1 H NMR和13 C NMR表征染料。结果表明,该染料的最大吸收波长均为590 nm左右,表明它们是一种蓝色染料。1 H NMR和1313 C NMR结果表明,染料结构中存在两种互变异构现象,蒽醌环与苯基偶氮键之间形成了新的共轭体系。密度泛函理论(DFT)的计算也证明了形成新的较大共轭体系的产生,蓝色是由该体系生成的。染料在棉布上的固色率超过88%,日晒牢度达到5级。
  • Methods for Producing Fluorine-Containing Hydroxyaldehyde, Fluorine-Containing Propanediol, and Fluorine-Containing Alcohol Monomer
    申请人:Central Glass Company, Limited
    公开号:US20150361026A1
    公开(公告)日:2015-12-17
    As shown by the following reaction formula, disclosed is a fluorine-containing hydroxyaldehyde production method, including the step of obtaining a fluorine-containing hydroxyaldehyde represented by the general formula (1) by reacting a fluorine-containing ketone represented by the general formula (4) and an aldehyde represented by the general formula (5) in the presence of an organic base selected from a heterocyclic compound which contains a nitrogen atom in its ring or a tertiary amine. By this production method, it is possible to obtain the fluorine-containing hydroxyaldehyde in a high yield. Furthermore, it is possible to easily obtain in high yields a fluorine-containing propanediol, which is a derivative of this fluorine-containing hydroxyaldehyde, and a fluorine-containing alcohol monomer by using the same.
    根据以下反应方程式,揭示了一种含氟羟基醛的生产方法,包括通过在选择的含氟酮(通式(4)表示)和醛(通式(5)表示)在含有从含有氮原子的杂环化合物或三级胺中选择的有机碱的情况下反应,获得由通式(1)表示的含氟羟基醛的步骤。通过这种生产方法,可以高产率地获得含氟羟基醛。此外,可以通过使用相同方法轻松高产率地获得含氟丙二醇(这是这种含氟羟基醛的衍生物)和含氟醇单体。
  • Enolate ion reactions of leucoquinizarin. Micheal additions
    作者:Gilles Arsenault、A. Douglas Broadbent、Peter Hutten-Czapski
    DOI:10.1039/c39830000437
    日期:——
    The base-catalysed reaction of leucoquinizarin with various Michael acceptors gives derivatives of potential value as anthracyclinone precursors.
    亮氨酸喹啉林与各种迈克尔受体的碱催化反应产生了潜在的衍生物,作为蒽环素酮前体。
  • Processes for producing fluorine-containing 2,4-diols and their derivatives
    申请人:Komata Takeo
    公开号:US20050215836A1
    公开(公告)日:2005-09-29
    A process for producing a fluorine-containing 2,4-diol represented by the formula [4], wherein R 1 represents a hydrogen atom or an acyclic or cyclic alkyl group having a carbon atom number of 1 to 7; R 2 represents an acyclic or cyclic alkyl group having a carbon atom number of 1 to 7, a phenyl group, or a substituted phenyl group; and R 1 and R 2 are optionally bonded to each other to form a ring, includes reducing a hydroxy ketone represented by the formula [3], wherein R 1 and R 2 are defined as above, by hydrogen in the presence of a ruthenium catalyst.
    生产一种由下式表示的含氟2,4-二醇的方法, 其中R1代表氢原子或具有1至7个碳原子的非环状或环状烷基基团;R2代表具有1至7个碳原子的非环状或环状烷基基团、苯基或取代苯基;且R1和R2可以选择地相互连接以形成环,包括在钌催化剂存在下用氢还原由下式表示的羟基酮, 其中R1和R2如上定义。
  • Process for producing alpha-substituted acrylic norbornanyyl compounds
    申请人:Komata Takeo
    公开号:US20050131248A1
    公开(公告)日:2005-06-16
    A process for producing an α-substituted acrylic norbornanyl compound represented by the formula [3] includes reacting an α-substituted acrylic acid anhydride represented by the formula [1] with a substituted norbornanyl alcohol represented by the formula [2]. wherein R 1 represents a hydrogen atom, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, fluoromethyl group, difluoromethyl group, trifluoromethyl group, or perfluoroethyl group, and wherein one of R 2 , R 3 and R 4 is a CF 3 C(CF 3 )(OH)CH 2 — group, and each of the other two of R 2 , R 3 and R 4 is a hydrogen.
    生产α-取代丙烯基莽环烷基化合物的过程如下:将式[1]表示的α-取代丙烯酸酐与式[2]表示的取代莽环烷基醇反应。 其中,R1代表氢原子、甲基、乙基、正丙基、异丙基、正丁基、仲丁基、叔丁基、氟甲基、二氟甲基、三氟甲基或全氟乙基;R2、R3和R4中的一个是CF3C(CF3)(OH)CH2—基团,另外两个是氢原子。
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同类化合物

齐斯托醌 黄决明素 马普替林杂质E(N-甲基马普替林) 马普替林杂质D 马普替林 颜料黄199 颜料黄147 颜料黄123 颜料黄108 颜料红89 颜料红85 颜料红251 颜料红177 颜料紫27 顺式-1-(9-蒽基)-2-硝基乙烯 阿美蒽醌 阳离子蓝3RL 长蠕孢素 镁蒽四氢呋喃络合物 镁蒽 锈色洋地黄醌醇 锂钠2-[[4-[[3-[(4-氨基-9,10-二氧代-3-磺基-1-蒽基)氨基]-2,2-二甲基-丙基]氨基]-6-氯-1,3,5-三嗪-2-基]氨基]苯-1,4-二磺酸酯 锂胭脂红 链蠕孢素 铷离子载体I 铝洋红 铂(2+)二氯化1-({2-[(2-氨基乙基)氨基]乙基}氨基)蒽-9,10-二酮(1:1) 钾6,11-二氧代-6,11-二氢-1H-蒽并[1,2-d][1,2,3]三唑-4-磺酸酯 钠6,11-二氧代-6,11-二氢-1H-蒽并[1,2-d][1,2,3]三唑-4-磺酸酯 钠4-({4-[乙酰基(乙基)氨基]苯基}氨基)-1-氨基-9,10-二氧代-9,10-二氢-2-蒽磺酸酯 钠2-[(4-氨基-9,10-二氧代-3-磺基-9,10-二氢-1-蒽基)氨基]-4-{[2-(磺基氧基)乙基]磺酰基}苯甲酸酯 钠1-氨基-9,10-二氢-4-[[4-(1,1-二甲基乙基)-2-甲基苯基]氨基]-9,10-二氧代蒽-2-磺酸盐 钠1-氨基-4-[(3-{[(4-甲基苯基)磺酰基]氨基}苯基)氨基]-9,10-二氧代-9,10-二氢-2-蒽磺酸酯 钠1-氨基-4-[(3,4-二甲基苯基)氨基]-9,10-二氧代-9,10-二氢-2-蒽磺酸酯 钠1-氨基-4-(1,3-苯并噻唑-2-基硫基)-9,10-二氧代蒽-2-磺酸盐 醌茜隐色体 醌茜素 酸性蓝127:1 酸性紫48 酸性紫43 酸性兰62 酸性兰25 酸性兰182 酸性兰140 酸性兰138 酸性兰 129 透明蓝R 透明蓝AP 透明红FBL 透明紫BS