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2,2,3,3-tetrafluoropropyloxymethyl thiirane | 1137575-85-9

中文名称
——
中文别名
——
英文名称
2,2,3,3-tetrafluoropropyloxymethyl thiirane
英文别名
2-[(3,3,2,2-Tetrafluoropropoxy)methyl]thiirane;2-(2,2,3,3-tetrafluoropropoxymethyl)thiirane
2,2,3,3-tetrafluoropropyloxymethyl thiirane化学式
CAS
1137575-85-9
化学式
C6H8F4OS
mdl
——
分子量
204.189
InChiKey
LLYJITONBIWXLP-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:
    79-80 °C(Press: 3 Torr)
  • 密度:
    1.344±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.1
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    34.5
  • 氢给体数:
    0
  • 氢受体数:
    6

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

  • 作为反应物:
    描述:
    2,2,3,3-tetrafluoropropyloxymethyl thiirane苯胺 反应 10.0h, 以61%的产率得到1-anilino-3-(2,2,3,3-tetrafluoropropyloxy)-propane-2-thiol
    参考文献:
    名称:
    [(Polyfluoroalkoxy)methyl]thiiranes and 2-anilinoethanethiols
    摘要:
    By reaction of appropriate oxiranes with thiourea [(polyfluoroalkoxy)methyl]-substituted thiiranes were obtained that are key compounds for the synthesis of perfluoro-containing 1,2-aminopropanethiols.
    DOI:
    10.1134/s1070428008070026
  • 作为产物:
    描述:
    3-(2,2,3,3-四氟丙氧基)-1,2-氧化丙烯硫脲 作用下, 以 甲醇 为溶剂, 以63%的产率得到2,2,3,3-tetrafluoropropyloxymethyl thiirane
    参考文献:
    名称:
    (烷氧基甲基)硫烷的热脱硫
    摘要:
    (烷氧基甲基)氧杂环戊烷与硫脲在甲醇中的反应得到了相应的噻喃,并且已经研究了产物的无催化剂热脱硫。脱硫的主要产物是醇和烯烃,在(聚氟烷氧基甲基)硫杂环丁烷及其非氟化类似物的情况下。在脱硫过程中,硫烷中较长的烷基链比烯烃的形成更有利于醇的形成。
    DOI:
    10.1134/s1070363214110139
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文献信息

  • A comparative study of the reactions of fluorinated oxi- and thiiranes with acyl chlorides
    作者:S. A. Nalet´ko、M. G. Pervova、M. I. Kodess、M. S. Toporova、T. I. Gorbunova、A. Ya. Zapevalov、V. I. Saloutin
    DOI:10.1007/s11172-017-1848-y
    日期:2017.6
    The CoCl2-catalyzed reactions of fluorinated 1,2-oxi- and thiiranes with acyl chlorides were studied. It was found that a regioselective heterocycle opening reaction resulted in two isomers having normal and abnormal structure in a ratio predetermined by the substituents in both the starting heterocycles and acyl chlorides.
    研究了 CoCl2 催化的化 1,2-氧杂和丙烷与酰的反应。发现区域选择性杂环开环反应产生具有正常和异常结构的两种异构体,其比例由起始杂环和酰中的取代基预先确定。
  • COMPOSITION AND POLYMER
    申请人:Asahi Kasei Kabushiki Kaisha
    公开号:EP2735581B1
    公开(公告)日:2021-07-14
  • SURFACE-TREATING AGENT FOR PATTERN FORMATION AND PATTERN-FORMING METHOD USING THE SURFACE-TREATING AGENT
    申请人:HOSHINO Wataru
    公开号:US20080241742A1
    公开(公告)日:2008-10-02
    A surface-treating agent for forming a resist pattern, includes: a compound represented by formula (1) as defined in the specification, wherein the surface-treating agent is used in a step between a formation of a first resist pattern on a first resist film and a formation of a second resist film on the first resist pattern to form a second resist pattern, and a pattern-forming method uses the surface-treating agent.
  • Composition and Polymer
    申请人:Nakamura Akitake
    公开号:US20140121293A1
    公开(公告)日:2014-05-01
    Disclosed is a composition comprising (A) at least one compound selected from the group consisting of an ether compound having two or more ether groups, a trivalent phosphorus compound, and a ketone compound, (B) a boron trihalide, and (C) an episulfide compound.
  • US9334371B2
    申请人:——
    公开号:US9334371B2
    公开(公告)日:2016-05-10
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同类化合物

硫化丙烯 环硫乙烷 异丁烯硫醚 反式-2,3-二乙炔基-噻丙环 乙烯基噻丙环 9-硫杂双环[6.1.0]壬-4-烯 8-硫杂双环[5.1.0]辛烷 3,4-环硫丁腈 2-(氯甲基)环硫乙烷 2,2,3-三甲基噻丙环 1-硫杂-螺[2.7]癸烷 1-氰基-3,4-环硫丁烷 1,3-壬二烯-1-基噻丙环 1,2-环硫-5-己烯 (甲氧基甲基)噻丙环 (S)-(-)-己基硫氯丙烷 (S)-(-)-1,2-环硫十二烷 1-tert-butoxy-3-methyl-siletane (2S,5R)-2,5-Bis-chloromethyl-2,5-dimethyl-[1,4]dithiane (2-chloro-3-butenyl)-thiirane 2-tert.-Butyl-2,3-dimethyl-thiiran 2,5-Bis-(cyan-methyl)-1,4-dithian 2,2,4,4-tetrakis(trifluoromethyl)thietane <2-Brom-allyl>-<2,3-epithio-propyl>-aether 1,7-Bis-(3,3-dimethyl-but-1-ynyl)-8,9-bis-[2,2-dimethyl-prop-(Z)-ylidene]-2,6-dithia-bicyclo[5.2.0]nonane (2S,3S)-2,3-epithio-1-hexanol nona-Si-methyl-Si,Si',Si''-[1,3,5,7]tetrathiocane-2,2,6-triyl-tris-silane 2-Methylthio-2-ethylthiiran 2,3,4,4-tetrachloro-2,3,5,5-tetrafluorothiolane 2-Diethoxymethyl-2-isopropyl-thiirane 2,4,6-tris-(7-methylamino-heptyl)-[1,3,5]trithiane, trihydrochloride 2-(1-Ethyl-pentyl)-thiirane (2R,3R)-2,3-epithio-3-cyclohexyl-1-propanol 2,3-epithio-2-methyl-pentan-1-ol N-tert-butyl-4,6,6-trimethylcyclohex-3-en-1-amine cis-2,3-Di-tert.-butylthiiran 2,2-diethylthiirane 9-aza-1-thioniabicyclo<3.3.>nonane triiodide (2R,3S)-2,3-epithio-1-undecanol 3,3'-Bithietanyliden trans-2,5-Dibrom-1,4-dithian Thioglycidylthiocyanat 2,4,6-tri-tert-butyl-1,3,5-trithiane (R)-Thiirancarbonsaeure 2-[(2,2,2-trifluoroethoxy)methyl]thiirane (R)-(+)-methylthiirane (E)-1,2-epithio-3-undecene 2,5-di-tert.-Butylthiophan 2,4,6-triundecyl-1,3,5-trithiane (r)-2,4,6-tri-tert-butyl-1,3,5-trithiane