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1,2,3-trifluoro-4,5,6-triazine | 112291-51-7

中文名称
——
中文别名
——
英文名称
1,2,3-trifluoro-4,5,6-triazine
英文别名
4,5,6-trifluoro-1,2,3-triazine;perfluoro-1,2,3-triazine;trifluoro-1,2,3-triazine;trifluoro-1,2,3-triazin;trifluorotriazine;4,5,6-trifluorotriazine
1,2,3-trifluoro-4,5,6-triazine化学式
CAS
112291-51-7
化学式
C3F3N3
mdl
——
分子量
135.048
InChiKey
JOENPVVANNJTIC-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

计算性质

  • 辛醇/水分配系数(LogP):
    0.3
  • 重原子数:
    9
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    38.7
  • 氢给体数:
    0
  • 氢受体数:
    6

SDS

SDS:213599471827c1ab5f52cce1d43ab6e3
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反应信息

  • 作为反应物:
    描述:
    1,2,3-trifluoro-4,5,6-triazine 700.0 ℃ 、10.67 Pa 条件下, 生成 1,2-二氟乙炔
    参考文献:
    名称:
    Isolation, characterization and some properties of free difluoroethyne, FCCF
    摘要:
    Difluoroethyne, FC = CF 1, has been prepared by vacuum pyrolysis of perfluoro-1,2,3-triazine, isolated in pure form and characterized by F-19 NMR and gas phase IR spectroscopy; its decomposition, with a half-life-time at 300 K and ca. 2.5 mbar of ca. 15 min, yields in the first step a polymer and: CF2, the latter either oligomerizing or reacting with 1 to form three different C3F4 isomers.
    DOI:
    10.1039/c39910000456
  • 作为产物:
    描述:
    4,5,6-三氯三嗪 在 potassium fluoride 作用下, 生成 1,2,3-trifluoro-4,5,6-triazine
    参考文献:
    名称:
    全氟烷基-1,2,3-三嗪:对环氮的新型亲核攻击
    摘要:
    描述了三氟-和全氟异丙基-1,2,3-三嗪衍生物的合成,以及全氟烷基阴离子和苯基溴化镁对环氮的不寻常亲核攻击;发生2,3-二甲基丁二烯向环氮的向亲性加成和2,3-二甲基丁-2-烯的类似加成。
    DOI:
    10.1039/c39870001697
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文献信息

  • Polyhalogenoheterocyclic compounds - 38.
    作者:Richard D. Chambers、Thomas Shepherd、Masayuki Tamura
    DOI:10.1016/s0040-4020(01)81709-9
    日期:1988.1
    3-triazine (1) with potassium fluoride at elevated temperatures gives trifluoro-l,2,3-triazine (4) and corresponding chlorofluoro derivatives. Introduction of perfluoroiso- propyl groups occurs, using fluoride ion and hexafluoropropene. A novel product (7) is described that arises from uucleophilic attack of perfluoroisopropyl anion on ring nitrogen in an intermediate triazine derivative.
    使三氯-1,2,3-三嗪(1)与氟化钾在高温下反应,得到三氟-1,2,3-三嗪(4)和相应的氯氟衍生物。使用氟离子和六氟丙烯引入全氟异丙基。描述了一种新产物(7),该产物是由全氟异丙基阴离子对中间体三嗪衍生物中环氮的亲核攻击而产生的。
  • Azetes from fluorinated 1,2,3-triazines
    作者:Richard D. Chambers、Masayuki Tamura、Thomas Shepherd、Clifford J. Ludman
    DOI:10.1039/c39870001699
    日期:——
    Strong evidence is presented for generation of azetes by photolysis of fluorinated 1,2,3-triazine derivatives; a monocyclic azete has been trapped chemically and another has been observed at low temperature by i.r. and mass spectroscopy.
    有强有力的证据表明,通过氟化1,2,3-三嗪衍生物的光解可以生成共沸物。化学上已经捕获了单环沸腾物,并且通过红外和质谱在低温下观察到了另一种。
  • Fibre reactive azo dyestuffs
    申请人:Bayer Aktiengesellschaft
    公开号:US05239063A1
    公开(公告)日:1993-08-24
    Fiber reactive azo dyestuffs of the formula ##STR1## in which R=H or C.sub.1 -C.sub.6 alkyl, which can be substituted with OH, Hal, SO.sub.3 H or OSO.sub.3 H; Z=heterocyclic five or six membered ring; n, m=0, 1 or 2, wherein n+m=0, 1 or 2; Y=OH, OR, NR.sub.2 R.sub.3, OMe; and R.sub.2, R.sub.3, =H, R and R.sub.2, R.sub.3 and N can form a heterocyclic 5 or 6-membered ring.
    化学式为##STR1##的纤维活性偶氮染料,其中R= H 或 C.sub.1 -C.sub.6烷基,可以用OH,Hal,SO.sub.3H或OSO.sub.3H取代; Z=杂环五元或六元环; n,m=0,1或2,其中n+m=0,1或2; Y= OH,OR,NR.sub.2R.sub.3,OMe; R.sub.2,R.sub.3= H,R和R.sub.2,R.sub.3和N可以形成杂环5或6元环。
  • Reactive dyestuffs containing hydroxy naphthalene disulphonic acids
    申请人:Bayer Aktiengesellschaft
    公开号:US05459246A1
    公开(公告)日:1995-10-17
    New reactive dyestuffs which, in the form of the free acid, correspond to the following formula ##STR1## wherein the substituents have the meaning given in the description, are suitable for dyeing and printing materials containing hydroxyl groups or amide groups, in particular cellulose materials.
    新的反应性染料,以游离酸的形式对应于以下公式##STR1##其中取代基在描述中给出的含义,适用于染色和印刷含有羟基或酰胺基团的材料,特别是纤维素材料。
  • Fluorotriazine containing naphthylazonaphthyl monoazo reactive dyes
    申请人:Bayer Aktiengesellschaft
    公开号:US05459245A1
    公开(公告)日:1995-10-17
    Reactive dyestuffs which, in the form of the free acid, have the following formula ##STR1## in which the substituents have the meaning given in the description, are suitable for the dyeing and printing of hydroxyl- and amido-containing materials, in particular cellulose materials.
    具有以下公式的自由酸形式的反应染料##STR1##其中取代基的含义如描述所述,适用于含有羟基和氨基的材料的染色和印刷,特别是纤维素材料。
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