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2,2,4-trifluoro-1,3-dioxole | 89414-03-9

中文名称
——
中文别名
——
英文名称
2,2,4-trifluoro-1,3-dioxole
英文别名
1,3-Dioxole, 2,2,4-trifluoro-
2,2,4-trifluoro-1,3-dioxole化学式
CAS
89414-03-9
化学式
C3HF3O2
mdl
——
分子量
126.035
InChiKey
MLTGZMHSEZRESX-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:
    -3.6±40.0 °C(Predicted)
  • 密度:
    1.54±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.4
  • 重原子数:
    8
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    18.5
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:4c181f7ecceb59aadaed27ffa3eb3926
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反应信息

  • 作为产物:
    描述:
    2,2,4-trifluoro-4,5-dichloro-1,3-dioxolane 、 mercury (II) chloride 在 magnesium 作用下, 以 四氢呋喃 为溶剂, 生成 2,2,4-trifluoro-1,3-dioxole
    参考文献:
    名称:
    Fluorodioxoles
    摘要:
    可能在4或5位置具有Cl或F取代基并在2位置具有两个F或CF.sub.3取代基的新型氟代二氧杂环烷是制备与四氟乙烯和偏氟乙烯的均聚物和共聚物以及与四氟乙烯和偏氟乙烯的三元聚合物的有用单体。该均聚物适用于玻璃材料,而共聚物则可用于耐腐蚀密封件,垫片和衬里等领域。
    公开号:
    US04535175A1
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文献信息

  • Fluorodioxoles
    申请人:E. I. Du Pont de Nemours and Company
    公开号:US04535175A1
    公开(公告)日:1985-08-13
    Novel fluorodioxoles which may have Cl or F substituents in the 4 or 5 positions and have two F or CF.sub.3 substituents in the 2 position are useful monomers for the preparation of homopolymers and copolymers with tetrafluoroethylene and terpolymers with tetrafluoroethylene and vinylidene fluoride. The homopolymers are suitable for glazing materials, while copolymers are useful, among others, for corrosion-resistant seals, gaskets, and linings.
    可能在4或5位置具有Cl或F取代基并在2位置具有两个F或CF.sub.3取代基的新型氟代二氧杂环烷是制备与四氟乙烯和偏氟乙烯的均聚物和共聚物以及与四氟乙烯和偏氟乙烯的三元聚合物的有用单体。该均聚物适用于玻璃材料,而共聚物则可用于耐腐蚀密封件,垫片和衬里等领域。
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同类化合物

1,4:6,9-二亚甲基吡啶联氮基[1,2-a]哒嗪(9CI) 1,3-苯并二氧戊环-4,7-二酮 1,3-二噁唑,4-甲基- 4,7-Dihydrobenzo[1,3]dioxole 1,3-Dioxole, 2,2-difluoro- 2,4-dimethyl-[1,3]dioxole 2-Methyl-1,3-dioxole 2,2,4-trifluoro-1,3-dioxole [1,3]Dioxolo[4,5-f][1,4]diazocine 2H-Thieno[3',4':3,4]cyclobuta[1,2-d][1,3]dioxole 2-tert-Butyl-4-methyl-2H-1,3-dioxole 2-(2H-1,3-Dioxol-2-ylidene)-2H-1,3-dioxole 1-(methoxycarbonyl)-2-methyl-4-isopropyl-3,5-dioxacyclopent-1-ene 5,6-Dimethyl-2H-1,3-benzodioxole-4,7-dione 4-Methyl-2-(1-methyl-butyl)-[1,3]dioxole 2-Hexyl-4-methyl-[1,3]dioxole 4-Methyl-2-pentyl-[1,3]dioxole 2-ethyl-4-methyl-1,3-dioxole ethyl 6H-cyclohepta[d][1,3]dioxole-6-carboxylate 2-acetyl-3-methyl-5-(2-furoyl)-3,5-dioxacyclopent-1-ene 4,5-dimethyl-1,3-dioxole (5aS)-5aH-[1,3]dioxolo[4,5-e]indazole (5aR)-5aH-[1,3]dioxolo[4,5-e]indazole 2-[(5R)-5-amino-4H-1,3-benzodioxol-5-yl]ethanol 2-[(5S)-5-amino-4H-1,3-benzodioxol-5-yl]ethanol methyl (2S)-2-methyl-1,3-dioxole-4-carboxylate N-[(2S)-2-(methoxymethyl)pyrrolidin-1-yl]-1,3-dioxole-4-carboxamide 3-(1,3-Dioxol-4-yl)prop-2-yn-1-ol Fluoroethane;fluoromethyl hypofluorite;2,2,4-trifluoro-5-(fluoromethoxy)-1,3-dioxole N-(oxolan-2-ylmethyl)-1,3-dioxole-4-carboxamide [(2,4-Difluoro-1,3-dioxol-2-yl)-difluoromethyl] hypofluorite;ethoxyethane [6-(1,3-Dioxol-4-ylmethylidene)cyclohexa-1,3-dien-1-yl]boronic acid 3,4-Dihydro-1,2-benzodioxol-7-one;hydrobromide methyl (2R)-2-methyl-1,3-dioxole-4-carboxylate 2,2-Difluoro-1,3-dioxole;ethane Difluoromethane;fluoroethane;fluoromethane;fluoromethyl hypofluorite;2,2,4-trifluoro-5-(fluoromethoxy)-1,3-dioxole 4-(2,3-Dihydrothiophen-2-yl)-1,3-dioxole 3-propyl-5,6,7,7a-tetrahydro-4H-1,2-benzodioxole-5-carboxylic acid 4-(3-Methoxybuta-1,3-dien-2-yl)-5-[1-(3-methoxy-2,4-dimethylpent-3-enoxy)ethenyl]-1,3-dioxole 4-Butyl-5-ethyl-1,3-dioxole 4-Ethyl-1,3-dioxole N-(1,3-dioxol-4-yl)acetamide Ethane;2-methylidene-1,3-dioxole 5-(2-Methylpropyl)-4,5-dihydro-1,3-benzodioxole 3-(1,3-Dioxol-2-yl)prop-2-enal (1-Carbamoylcyclobutyl) 1,3-dioxole-4-carboxylate 4-(Cyclohexa-1,3-dien-1-ylmethyl)-1,3-dioxole [Difluoro-(2,4,5-trifluoro-1,3-dioxol-2-yl)methyl] hypofluorite;2-ethoxy-1,1,1-trifluoroethane 2-Hepta-1,3-dienyl-1,3-dioxole 4-Methylsulfanyl-5-propan-2-yl-1,3-dioxole