2,2-difluoro-3-iodopropionyl fluoride | 99497-42-4

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 酰卤
• 英文名称: 2,2-difluoro-3-iodopropionyl fluoride
• 英文别名: 2,2-Difluoro-3-iodopropionic acid fluoride；2,2-difluoro-3-iodopropanoyl fluoride
• CAS: 99497-42-4
• 化学式: C₃H₂F₃IO
• 分子量: 237.948
• InChiKey: PDHOBUTUQJLFJF-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2
• 重原子数：
  8
• 可旋转键数：
  2
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.67
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  2,2-difluoro-3-iodopropionyl fluoride 生成 2-氟丙烯酸
  参考文献：
  名称：

  SUEHFUDZI, MASAXIRO

  摘要：

  DOI：
• 作为产物：
  描述：

  2,2,3,3-四氟环氧丙烷 在 sodium iodide 作用下， 以 水 为溶剂， 生成 2,2-difluoro-3-iodopropionyl fluoride
  参考文献：
  名称：

  Fluorine-containing olefin, fluorine-containing polymer and

  摘要：

  提供一种含氟烯烃，例如CH.sub.2 .dbd.CFCF.sub.2 --R.sub.f.sup.6 --(CH.sub.2).sub.k --X.sup.2 [其中，X.sup.2为##STR1##，R.sub.f.sup.6为含1至40个碳原子的氟代含氟烷基或--OR.sub.f.sup.7--(Rf.sup.7为含1至40个碳原子的氟代含氟烷基或含3至50个碳原子的氟代含氟醚基)，k为0或1至6的整数]；通过聚合上述烯烃制备的含氟功能性基团的聚合物，与各种耐热热塑性树脂具有良好的亲和性，并能与热塑性树脂形成均匀分散物；以及包括上述含氟功能性基团聚合物和芳香族聚酯或类似物作为耐热热塑性树脂的热塑性树脂组合物。

  公开号：

  US05986150A1

文献信息

• 2,2-difluoropropionic acid derivatives
  申请人：Daikin Industries Ltd.

  公开号：US04719052A1

  公开（公告）日：1988-01-12

  2,2,3-trifluoropropionyl fluoride is prepared by opening the ring of tetrafluorooxetane in the presence of a catalyst. Analogously, a novel 2,2-difluoropropionic acid derivative of the formula: XCH.sub.2 CF.sub.2 COY (I) wherein X is chlorine, bromine, iodine, a group of the formula: R.sub.1 O-- (II) or R.sub.2 COO-- (III) wherein R.sub.1 R.sub.2 are each an aliphaic or halogenated aliphatic hydrocarbon group having 1 to 8 carbon atoms or an aromatic hydrocarbon group having 6 to 8 carbon atoms optionally bearing at least one substituent, or a group of the formula: X'CH.sub.2 CF.sub.2 CF.sub.2 O-- (IV) wherein X' is fluorine, chlorine, bromine, iodine, the group of the formula: R.sub.1 O--or R.sub.2 COO--; and Y is fluorine or a group of the formula: --OR.sub.3 (V) wherein R.sub.3 is an aliphatic or halogenated aliphatic hydrocarbon group having 1 to 8 carbon atoms except a perfluorohydrocarbon group or an aromatic hydrocarbon group having 6 to 8 carbon atoms optionally bearing at least one substituent or of the formula : --OCH.sub.2 R.sub.f (V') wherein R.sub.f is an aliphatic perfluorohydrocarbon having 1 to 7 carbon atoms is prepared.

  2,2,3-三氟丙酰氟是在催化剂存在下打开四氟氧杂环的环来制备的。类似地，通过以下式子的新型2,2-二氟丙酸衍生物制备：XCH.sub.2 CF.sub.2 COY (I)，其中X为氯、溴、碘、式：R.sub.1 O-- (II)或R.sub.2 COO-- (III)的基团，其中R.sub.1和R.sub.2均为具有1至8个碳原子的脂肪或卤代脂肪烃基或具有6至8个碳原子的芳香烃基，可选地带有至少一个取代基，或式：X'CH.sub.2 CF.sub.2 CF.sub.2 O-- (IV)的基团，其中X'为氟、氯、溴、碘、式：R.sub.1 O--或R.sub.2 COO--；Y为氟或式：--OR.sub.3 (V)的基团，其中R.sub.3为具有1至8个碳原子的脂肪或卤代脂肪烃基，但不包括全氟碳氢基团或具有6至8个碳原子的芳香烃基，可选地带有至少一个取代基，或式：--OCH.sub.2 R.sub.f (V')，其中R.sub.f为具有1至7个碳原子的脂肪全氟碳氢基团来制备。
• Novel fluorovinyl ether and copolymer comprising the same
  申请人：Daikin Industries, Ltd.

  公开号：US05001278A1

  公开（公告）日：1991-03-19

  A fluorovinyl ether of the formula: XCH.sub.2 CF.sub.2 CF.sub.2 --(OCH.sub.2 CF.sub.2 CF.sub.2).sub.m --(OCFYCF.sub.2).sub.n --OCF.dbd.CF.sub.2 (I) wherein X is a hydrogen atom or a halogen atom (e.g. fluorine, chlorine, bromine and iodine); Y is a fluorine atom or a trifluoromethyl group; m is an integer of 0 to 5; and n is 0, 1 or 2, which can modify a polymer of at least one ethylenically unsaturated compound.

  化学式为：XCH.sub.2 CF.sub.2 CF.sub.2 --(OCH.sub.2 CF.sub.2 CF.sub.2).sub.m --(OCFYCF.sub.2).sub.n --OCF.dbd.CF.sub.2（I）的氟乙烯醚，其中X是氢原子或卤素原子（如氟、氯、溴和碘）；Y是氟原子或三氟甲基基团；m是0到5的整数；n是0、1或2，可改性至少一种乙烯基不饱和化合物的聚合物。
• Polyelectrolytic Behavior of a Novel Fluorine-Containing Ionomer, PPFNA
  作者：Akira Minakata、Kuniko Takayama、Shin-ichi Yano、Yoshito Tanaka、Takayuki Araki、Tetsuo Shimizu

  DOI：10.1021/jp0224923

  日期：2003.8.1

  Solution properties of a novel fluorine-containing ionomer PPFNA were studied by pH titration, conductivity, and viscosity measurements. This polymer is a poly(carboxylic acid) but dissociates strongly, resulting in a low pH value and a high specific conductance at low degrees of neutralization. When the solution was neutralized with NaOH, the conductance decreased sharply at first and then decreased gradually until full neutralization. This conductometric titration profile indicates that this polymer is a fairly strong polyelectrolyte but not a typical strong one such as poly(styrene sulfonic acid) or aliphatic ionenes. The pH measurement showed that this polymer is a strong polyacid, although the titration profile changed slightly upon the addition of salt. The reduced viscosity of the salt-free solution was well fitted to Fuoss' equation, specific to polyelectrolyte solutions. Upon the addition of salt, however, the viscosity-neutralization profile became rather similar to that of weak polyacid, and the concentration dependence of the reduced viscosity shifted gradually to that of nonionic polymer solutions. The corresponding monomer behaves like a completely strong acid, in contrast to the polymer, especially in conductometric titration.
• OHSAKA, JOHNOSUKE;TONZUKA, TAKASHI;TAKAKI, SHOJI;NEGISHI, JOSHIO
  作者：OHSAKA, JOHNOSUKE、TONZUKA, TAKASHI、TAKAKI, SHOJI、NEGISHI, JOSHIO

  DOI：——

  日期：——