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3-ethoxy-xanthen-9-one | 100914-96-3

中文名称
——
中文别名
——
英文名称
3-ethoxy-xanthen-9-one
英文别名
3-Aethoxy-xanthen-9-on;3-Ethoxyxanthen-9-one
3-ethoxy-xanthen-9-one化学式
CAS
100914-96-3
化学式
C15H12O3
mdl
——
分子量
240.258
InChiKey
BRFITOYKMVEOCL-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

  • 沸点:
    398.4±31.0 °C(Predicted)
  • 密度:
    1.237±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.9
  • 重原子数:
    18
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

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

  • 一种高效长寿命的有机室温磷光材料及其制 备方法
    申请人:北京师范大学
    公开号:CN108997299B
    公开(公告)日:2020-04-03
    本申请提供一种烷氧基、苄氧基或溴取代的占吨酮衍生物及其制备方法,该占吨酮衍生物制备方法简单,磷光峰位位于长波长峰位,其磷光寿命长,且发光效率高。该占吨酮衍生物的制备步骤包括:步骤1:向反应容器中加入苯酚,碳酸钾,DMF及甲苯,于氮气环境下回流3‑5小时,进行脱水处理直至确认体系中无水产生为止;之后,去除甲苯,恢复至室温,加入4‑溴‑2‑氟苯腈,于氮气环境下回流3‑5小时;反应结束后,向溶液中加入甲苯100mL加以稀释,然后过滤、水洗、干燥,得到晶体粗产物,经色谱柱纯化得到中间体步骤2:加入步骤1所得到的中间体,水,硫酸,在氮气环境下加热至150℃‑200℃温度搅拌回流10‑15小时;反应结束后,冷却至室温,加入到水中稀释,然后用三氯甲烷和饱和氯化钠溶液萃取,将有机相合并,干燥过滤,减压蒸馏除去溶剂,得到晶体粗产物,经色谱柱纯化得到白色晶体
  • 859. Xanthones: cyclisation of 3′-substituted 2-carboxydiphenyl ethers
    作者:A. A. Goldberg、A. H. Wragg
    DOI:10.1039/jr9580004227
    日期:——
  • PHOTOSENSITIVE RESIN COMPOSITION, PHOTOSENSITIVE ELEMENT, CURED PRODUCT, SEMICONDUCTOR DEVICE, METHOD FOR FORMING RESIST PATTERN, AND METHOD FOR PRODUCING CIRCUIT SUBSTRATE
    申请人:Hitachi Chemical Company, Ltd.
    公开号:US20170329220A1
    公开(公告)日:2017-11-16
    A photosensitive resin composition comprises: a resin having a phenolic hydroxyl group; a photosensitive acid generator; a compound having at least one selected from the group consisting of an aromatic ring, a heterocycle and an alicycle, and at least one selected from the group consisting of a methylol group and an alkoxyalkyl group; an aliphatic compound having two or more functional groups being at least one selected from the group consisting of an acryloyloxy group, a methacryloyloxy group, a glycidyloxy group, an oxetanyl alkyl ether group, a vinyl ether group and a hydroxyl group; and a compound having at least one skeleton selected from the group consisting of an anthracene skeleton, a phenanthrene skeleton, a pyrene skeleton, a perylene skeleton, a carbazole skeleton, a phenothiazine skeleton, a xanthone skeleton, a thioxanthone skeleton, an acridine skeleton, a phenylpyrazoline skeleton, a distyrylbenzene skeleton and a distyrylpyridine skeleton, or a benzophenone compound.
  • US4379039A
    申请人:——
    公开号:US4379039A
    公开(公告)日:1983-04-05
  • Stereocontrolled synthesis of a d-amicetose functionalised tetrahydroxanthone related to kigamicin A
    作者:Penelope A. Turner、Samiullah、Jacqueline L. Whatmore、Michael Shipman
    DOI:10.1016/j.tetlet.2013.09.091
    日期:2013.11
    A glycosylated tetrahydroxanthone mimicking the ABC subunit of kigamicin A is synthesised in five steps by a sequence that exploits a Pd catalysed C-O bond forming reaction to construct the tetrahydroxanthone nucleus; chemo- and enantioselective Ru-catalysed transfer hydrogenation to establish the C-14 hydroxyl stereochemistry in the A-ring; and a trichloroacetimidate activated donor to introduce the beta-linked D-amicetose unit in a stereoselective manner. (C) 2013 Elsevier Ltd. All rights reserved.
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