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Phenylthiodibenzoylmethan | 28195-12-2

中文名称
——
中文别名
——
英文名称
Phenylthiodibenzoylmethan
英文别名
1,3-Diphenyl-2-phenylthio-1,3-propandion;1,3-Diphenyl-2-phenylsulfanylpropane-1,3-dione
Phenylthiodibenzoylmethan化学式
CAS
28195-12-2
化学式
C21H16O2S
mdl
——
分子量
332.423
InChiKey
KCDSITQPJDIUEI-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:
    86 °C(Solv: hexane (110-54-3))
  • 沸点:
    519.8±45.0 °C(Predicted)
  • 密度:
    1.24±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    5.5
  • 重原子数:
    24
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    59.4
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为反应物:
    描述:
    Phenylthiodibenzoylmethanchloramine-B丙酮 为溶剂, 反应 4.0h, 以86.2%的产率得到N-(1-Benzoyl-2-oxo-2-phenyl-1-phenylsulfanyl-ethyl)-benzenesulfonamide
    参考文献:
    名称:
    Koval', I. V.; Andrushchenko, V. V.; Kremlev, M. M., Journal of Organic Chemistry USSR (English Translation), 1982, vol. 18, p. 730 - 734
    摘要:
    DOI:
  • 作为产物:
    描述:
    Bis(phenylthio)dibenzoylmethan 以65%的产率得到
    参考文献:
    名称:
    PADMANABHAN, SEETHARAMAIYER;OGAWA, TAKUJI;SUZUKI, HITOMI, J. CHEM. RES. (S),(1989) N, C. 266-267
    摘要:
    DOI:
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文献信息

  • PROCESS FOR PRODUCING ALKOXYCARBONYLFLUOROALKANESULFONATES
    申请人:FUJIWARA Masaki
    公开号:US20080108846A1
    公开(公告)日:2008-05-08
    A process for producing an alkoxycarbonylfluoroalkanesulfonate represented by the formula [1] is provided. This process includes the steps of (a) reacting a halofluoroalkanoate represented by the formula [2], with a sulfinating agent, thereby obtaining an alkoxycarbonylfluoroalkanesulfinate represented by the formula [3]; and (b) reacting the alkoxycarbonylfluoroalkanesulfinate with an oxidizing agent, thereby obtaining the target alkoxycarbonylfluoroalkanesulfonate. Furthermore, it is possible to react the obtained alkoxycarbonylfluoroalkanesulfonate with a monovalent onium salt to conduct a salt exchange, thereby obtaining a alkoxycarbonylfluoroalkanesulfonic acid onium salt represented by the formula [4].
    提供了一种制备由公式[1]表示的烷氧羰基氟代烷磺酸盐的方法。这个过程包括以下步骤:(a)使由公式[2]表示的卤氟代烷酸盐与亚磺化剂反应,从而获得由公式[3]表示的烷氧羰基氟代烷亚磺酸盐;以及(b)使烷氧羰基氟代烷亚磺酸盐与氧化剂反应,从而获得目标烷氧羰基氟代烷磺酸盐。此外,可以将获得的烷氧羰基氟代烷磺酸盐与单价阳离子盐进行反应,进行盐交换,从而获得由公式[4]表示的烷氧羰基氟代烷磺酸阳离子盐。
  • Compound for Photoacid Generator, Resist Composition Using the Same, and Pattern-Forming Method
    申请人:Central Glass Company, Limited
    公开号:US20130130175A1
    公开(公告)日:2013-05-23
    A sulfonic acid onium salt represented by the following formula (1) useful as a superior radiosensitive acid generator for resist compositions. It is possible to form a good pattern by using a resist composition containing this sulfonic acid onium salt corresponding to the formula (1): in which R 1 represents a monovalent organic group, and Q + represents a sulfonium cation or iodonium cation.
    以下是用作优良的辐射敏感性酸发生剂的磺酸醋銨盐的化学式(1)。通过使用含有与化学式(1)对应的磺酸醋銨盐的抗蚀组合物,可以形成良好的图案: 其中R1代表一价有机基团,Q+代表磺銨阳离子或碘銨阳离子。
  • Sulfenylation of Active Methylene Compounds with Sulfenamides
    作者:Takanobu Kumamoto、Susumu Kobayashi、Teruaki Mukaiyama
    DOI:10.1246/bcsj.45.866
    日期:1972.3
    secondary alkylamines with active methylene compounds afforded mono-sulfenylated compounds in good yields. The reactions of 2 mol of sulfenamides derived from imides with 1 mol of active methylene compounds in the presence of a base gave di-sulfenylated compounds. It was found that α-mono-sulfenylated ketones were prepared by the reactions of enamines with sulfenamides derived from imides. α-gem-Di-sulfenylated
    衍生自仲烷基胺的次磺酰胺与活性亚甲基化合物的等摩尔反应以良好的产率提供单次磺酰化的化合物。2 mol 衍生自酰亚胺的次磺酰胺与 1 mol 活性亚甲基化合物在碱存在下反应,得到二亚磺酰化化合物。发现α-单-亚磺酰化酮是通过烯胺与衍生自酰亚胺的次磺酰胺反应制备的。α-gem-Di-sulfenylated 酮是通过 α-mono-sulfenylated 酮与衍生自酰亚胺的亚磺酰胺在碱存在下反应制备的。还研究了N-苯基硫代苯甲脒盐酸盐的制备和反应。
  • Sodium Telluride-Mediated Sulfenylation of α-Halo Carbonyl Compounds with Diphenyl Disulfide
    作者:Seetharamaiyer Padmanabhan、Takuji Ogawa、Hitomi Suzuki
    DOI:10.1246/bcsj.62.1358
    日期:1989.4.15
    Under mild aprotic conditions α-halo carbonyl compounds react with diphenyl disulfide in the presence of sodium telluride to give the corresponding α-phenylthio derivatives in good to moderate yields. The reaction appears to proceed involving the sulfur–sulfur bond cleavage of diphenyl disulfide by sodium telluride.
    在温和的非质子惰性条件下,α-卤代羰基化合物在碲化钠存在下与二苯基二硫化物反应,以良好到中等的产率得到相应的 α-苯硫基衍生物。该反应似乎涉及碲化钠对二苯基二硫化物的硫-硫键裂解。
  • SULFONIC ACID DERIVATIVE AND PHOTOACID GENERATOR
    申请人:Hosoi Yasuhiro
    公开号:US20120289738A1
    公开(公告)日:2012-11-15
    A sulfonic acid derivative represented by the following general formula (1): [Chemical formula 1] RCOOCH 2 CH 2 CFHCF 2 SO 3 − M + (1) where R represents a substituted or unsubstituted C 1-30 linear, branched, or cyclic hydrocarbon group, or a substituted or unsubstituted C 6-30 aryl group, and M + represents a counter cation.
    化学式(1)表示的磺酸衍生物如下:[化学式1]RCOOCH2CH2CFHCF2SO3−M+(1),其中R表示取代或未取代的C1-30线性、支链或环烃基,或取代或未取代的C6-30芳基;M+表示反离子。
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