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1,8-二氯-9,10-双(苯乙炔基)蒽 | 51749-83-8

中文名称
1,8-二氯-9,10-双(苯乙炔基)蒽
中文别名
1,8-二氯-9,10-二苯乙炔基蒽;1,8-二氯-9,10-二苯乙炔基蒽(DBEA);1,8-二氯-9,10-双苯乙炔蒽;1,8-二氯-9,1-二苯乙炔基蒽;DBEA
英文名称
1,8-dichloro-9,10-bis(phenylethynyl)anthracene
英文别名
1,8-dichloro-9,10-bis(2-phenylethynyl)anthracene
1,8-二氯-9,10-双(苯乙炔基)蒽化学式
CAS
51749-83-8
化学式
C30H16Cl2
mdl
MFCD00012048
分子量
447.363
InChiKey
YONGNHJIWAYNLC-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:
    168-170 °C(lit.)
  • 沸点:
    524.89°C (rough estimate)
  • 密度:
    1.0703 (rough estimate)
  • 稳定性/保质期:
    <p>遵照规定使用和储存,则不会分解。</p>

计算性质

  • 辛醇/水分配系数(LogP):
    9.7
  • 重原子数:
    32
  • 可旋转键数:
    4
  • 环数:
    5.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

安全信息

  • 危险品标志:
    Xn
  • 危险类别码:
    R40,R36/37/38,R20/21/22
  • 海关编码:
    2903999090
  • 安全说明:
    S26,S36/37/39,S45
  • 危险性防范说明:
    P280,P305+P351+P338
  • 危险性描述:
    H302

反应信息

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文献信息

  • Reagents and methods for direct labeling of nucleotides
    申请人:Naleway John J.
    公开号:US20130150254A1
    公开(公告)日:2013-06-13
    The present invention provides systems and methods for production of activatable diazo-derivatives for use in labeling nucleotides. Labeling nucleotides is accomplished by contacting a stable hydrazide derivative of a detectable moiety with an activating polymer reagent which is used to directly label the nucleotide sample. Labeling occurs on the phosphate backbone of the nucleotide which does not perturb hybridization of the labeled nucleotide with its anti-sense strand. Since the method involves direct labeling, all types of nucleotides can be labeled without prior amplification or alteration.
    本发明提供了用于生产可激活重氮衍生物以用于标记核苷酸的系统和方法。通过将可检测基团的稳定的肼酰肼衍生物与用于直接标记核苷酸样品的活化聚合物试剂接触来完成核苷酸的标记。标记发生在核苷酸的磷酸骨架上,不会干扰标记核苷酸与其反义链的杂交。由于该方法涉及直接标记,所有类型的核苷酸都可以在不经过扩增或改变的情况下进行标记。
  • Blue/violet diphenylanthracene chemiluminescent fluorescers
    申请人:Cranor Earl
    公开号:US20100327240A1
    公开(公告)日:2010-12-30
    Compounds are disclosed for the production of chemiluminescent light, particularly for the production of blue/violet light within the range of about 390 nm to less than 438 nm, and most particularly to the use of compounds composed of symmetrically and asymmetrically substituted anthracenes which are effective for increasing the production of such blue/violet light when used as fluorescers in conjunction with chemiluminescent systems. These systems utilize derivatives of 9,10-diphenylanthracene containing one or more fluorines As shown in General Formulae 1-3. The variables shown in Formulae 1-3 are defined in the specification.
    揭示了用于生产化学发光灯的化合物,特别是用于在约390纳米至不到438纳米范围内产生蓝/紫光的化合物,尤其是使用由对称和非对称取代的蒽组成的化合物,这些化合物在与化学发光系统一起作为荧光剂时有效地增加了这种蓝/紫光的产生。这些系统利用含有一个或多个氟的9,10-二苯基蒽衍生物,如通用公式1-3所示。公式1-3中显示的变量在说明书中有定义。
  • Method for producing aqueous polymer dispersions containing colorants
    申请人:Mathauer Klemens
    公开号:US20050075453A1
    公开(公告)日:2005-04-07
    The present invention relates to a process for preparing dye-comprising aqueous polymer dispersions by free-radical aqueous emulsion polymerization of ethylenically unsaturated monomers in the presence of free-radical initiators, in which at least some of the monomers are employed in the form of an oil-in-water emulsion E1 whose disperse phase comprises at least one oil-soluble dye, wherein the disperse phase of E1 is formed essentially of dye-comprising monomer droplets having a diameter<500 nm. The present invention also relates to perylene dyes of the formula III as set forth in claim 35. The present invention relates in addition to dye-comprising formulations which comprise the dye-comprising polymers of the invention and to pigmented formulations which comprise a polymer of the invention comprising optical brightener.
    本发明涉及一种制备含染料的水性聚合物分散体的工艺,通过自由基水性乳液聚合乙烯基不饱和单体,在自由基引发剂的存在下进行,其中至少有一些单体以E1油包水乳液的形式使用,其分散相包含至少一种油溶性染料,其中E1的分散相基本上由直径小于500 nm的含染料单体液滴形成。本发明还涉及公式III所述的苝染料。此外,本发明还涉及包含本发明的染料聚合物的染料组合物以及包含一种具有光学增白剂的本发明聚合物的颜料组合物。
  • REAGENTS AND METHODS FOR DIRECT LABELING OF NUCLEOTIDES
    申请人:MARKER GENE TECHNOLOGIES, INC.
    公开号:US20150152476A1
    公开(公告)日:2015-06-04
    The present invention provides systems and methods for production of activatable diazo-derivatives for use in labeling nucleotides. Labeling nucleotides is accomplished by contacting a stable hydrazide derivative of a detectable moiety with an activating polymer reagent which is used to directly label the nucleotide sample. Labeling occurs on the phosphate backbone of the nucleotide which does not perturb hybridization of the labeled nucleotide with its anti-sense strand. Since the method involves direct labeling, all types of nucleotides can be labeled without prior amplification or alteration.
    本发明提供了用于生产可激活的重氮衍生物以用于标记核苷酸的系统和方法。标记核苷酸是通过将可检测基团的稳定肼基衍生物与用于直接标记核苷酸样品的活化聚合物试剂接触来完成的。标记发生在核苷酸的磷酸骨架上,不会干扰标记核苷酸与其反义链的杂交。由于该方法涉及直接标记,因此所有类型的核苷酸都可以在不进行扩增或改变的情况下进行标记。
  • A method for protecting the liquid components of a chemiluminescent system and a chemiluminescent light-generating system thus protected
    申请人:AMERICAN CYANAMID COMPANY
    公开号:EP0011911A1
    公开(公告)日:1980-06-11
    In a chemiluminescent lighting system having separated components in storage before use, at least one of the separate components is stored in a container made from a laminate of polypropylene film and aluminium foil. Good stability of both oxalate ester components and hydroperoxide components when stored in such containers is demonstrated.
    在一种化学发光照明系统中,在使用前的贮存过程中,其组分是分开的,其中至少有一种组分是贮存在一个由聚丙烯薄膜和铝箔层压板制成的容器中。事实证明,草酸酯成分和过氧化氢成分在这种容器中储存时具有良好的稳定性。
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表征谱图

  • 氢谱
    1HNMR
  • 质谱
    MS
  • 碳谱
    13CNMR
  • 红外
    IR
  • 拉曼
    Raman
hnmr
mass
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ir
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  • 峰位数据
  • 峰位匹配
  • 表征信息
Shift(ppm)
Intensity
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Assign
Shift(ppm)
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测试频率
样品用量
溶剂
溶剂用量
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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