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hexyl-phosphonous dichloride | 6460-28-2

中文名称
——
中文别名
——
英文名称
hexyl-phosphonous dichloride
英文别名
dichlorohexylphosphine;dichloro-hexyl-phosphine;Dichlor-hexyl-phosphin;Hexyl-dichlor-phosphin;Hexyl-dichlorphosphin;Hexyldichlorphosphin;Dichloro(hexyl)phosphane
hexyl-phosphonous dichloride化学式
CAS
6460-28-2
化学式
C6H13Cl2P
mdl
——
分子量
187.049
InChiKey
VSIXVJCCVXXRCW-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):
    3.8
  • 重原子数:
    9
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

反应信息

  • 作为反应物:
    描述:
    hexyl-phosphonous dichloride吡啶 作用下, 生成 ethylenebis(hexylphosphinic acid)
    参考文献:
    名称:
    Mastalerz,P.; Tyka,R., Roczniki Chemii, 1964, vol. 38, p. 1529 - 1531
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Bliznyuk,N.K. et al., Journal of general chemistry of the USSR, 1967, vol. 37, p. 840 - 841
    摘要:
    DOI:
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文献信息

  • A new method for the synthesis of dichlorophosphines
    作者:Alexander N. Tavtorkin、Sofia A. Toloraya、Eduard E. Nifant’ev、Ilya E. Nifant’ev
    DOI:10.1016/j.tetlet.2010.12.048
    日期:2011.2
    A new method for the synthesis of alkyldichlorophosphines by chlorination of alkylphosphines with phosphorus pentachloride under mild conditions is described.
    描述了一种在温和条件下用五氯化磷氯化烷基膦来合成烷基二氯膦的新方法。
  • METHOD FOR PRODUCING AMIDE COMPOUND
    申请人:Kugimoto Junichi
    公开号:US20110313149A1
    公开(公告)日:2011-12-22
    This invention relates to a process for producing an amide compound by Beckmann rearrangement of an oxime compound using a compound having at least two electron-withdrawing leaving groups as a rearrangement catalyst, the process comprising a pre-preparation step in which the rearrangement catalyst and at least a part of the oxime compound are mixed and reacted; and a rearrangement reaction step in which the oxime compound is rearranged at a temperature higher than that in the pre-preparation step.
    本发明涉及一种通过使用至少具有两个电子吸引离去基团的化合物作为重排催化剂,通过贝克曼重排反应氧肟化合物生产酰胺化合物的方法,该方法包括预制备步骤,在该步骤中,将重排催化剂和至少一部分氧肟化合物混合并反应;以及重排反应步骤,在该步骤中,氧肟化合物在高于预制备步骤的温度下重排。
  • Ferrocenediphosphines
    申请人:Chen Weiping
    公开号:US20090124812A1
    公开(公告)日:2009-05-14
    Compounds of the formula I in the form of enantiomerically pure diastereomers or a mixture of diastereomers, (I), where the radicals R 1 are identical or different and are each C 1 -C 4 -alkyl; m is 0 or an integer from 1 to 3; n is 0 or an integer from 1 to 4; R 2 is a hydrocarbon radical or a C-bonded heterohydrocarbon radical; Cp is unsubstituted or C 1 -C 4 -alkyl-substituted cyclopentadienyl; Y is a C-bonded chiral group which directs metals of metallation reagents into the ortho position; and Phos is a P-bonded P(III) substituent. The compounds are chiral ligands for complexes of transition metals which are used as homogeneous catalysts in asymmetric syntheses.
    化学式为I的化合物形式为对映纯的非对映异构体或非对映异构体的混合物,其中基团R1相同或不同,且均为C1-C4烷基;m为0或1至3的整数;n为0或1至4的整数;R2为碳氢基团或C键结合的杂环碳氢基团;Cp为未取代或C1-C4烷基取代的环戊二烯基;Y为C键结合的手性基团,可将金属化试剂导向邻位位置;Phos为P键结合的P(III)取代基。这些化合物是过渡金属配合物的手性配体,用作不对称合成中的均相催化剂。
  • HETEROACENE DERIVATIVE, TETRAHALOTERPHENYL DERIVATIVE, AND PROCESSES FOR PRODUCING THE SAME
    申请人:Watanabe Makoto
    公开号:US20090261300A1
    公开(公告)日:2009-10-22
    There are provided a heteroacene derivative having an excellent oxidation resistance and capable of forming a semiconductor active phase by a coating process, and an oxidation-resistant organic semiconductor material using the same, as well as an organic thin film. [Means for Resolution] A heteroacene derivative represented by the formula (1) is obtained by tetrametalation of a tetrahaloterphenyl derivative with a metalation agent and subsequent treatment of the resulting compound with reaction agents: wherein the substituents R 1 to R 4 are the same or different and each represents a hydrogen atom, a fluorine atom, a chlorine atom, an aryl group having 4 to 30 carbon atoms, an alkyl group having 3 to 20 carbon atoms, or a halogenated alkyl group having 1 to 20 carbon atoms; T 1 and T 2 are the same or different and each represents sulfur, selenium, tellurium, oxygen, phosphorus, boron, or aluminum; l and m each is an integer of 0 or 1; and rings A and B are the same or different and each has a structure represented by the following formulae (A- 1 ) or (A-2).
    提供了一种具有优异氧化抗性并能够通过涂层工艺形成半导体活性相的杂环芳烃衍生物以及使用该衍生物的抗氧化有机半导体材料,以及有机薄膜。[解决方案] 通过使用金属化试剂四甲基化四卤代苯衍生物并随后用反应试剂处理所得化合物,获得了由式(1)表示的杂环芳烃衍生物:其中取代基R1至R4相同或不同,每个代表氢原子、氟原子、氯原子、具有4至30个碳原子的芳基、具有3至20个碳原子的烷基或具有1至20个碳原子的卤代烷基;T1和T2相同或不同,每个代表硫、硒、碲、氧、磷、硼或铝;l和m各自为0或1的整数;环A和环B相同或不同,每个具有以下式(A-1)或(A-2)所表示的结构。
  • A Robust, Divalent, Phosphaza-bicyclo[2.2.2]octane Connector Provides Access to Cage-Dense Inorganic Polymers and Networks
    作者:Joseph Bedard、Thomas G. Linford-Wood、Benedict C. Thompson、Ulrike Werner-Zwanziger、Katherine M. Marczenko、Rebecca A. Musgrave、Saurabh S. Chitnis
    DOI:10.1021/jacs.3c00882
    日期:——
    elimination to give high molecular weight (30 000–70 000 g mol–1), solution-processable polymers that form free-standing films. The end groups of the polymers could be tuned to engender orthogonal reactivity and form block copolymers. Networked cage-dense materials could be accessed by using PCl3 as a tritopic P(III) linker. Detailed mechanistic studies implicate a stepwise polycondensation that proceeds
    虽然主链中含有链状或环状基序的聚合物无处不在,但含有明确分子笼的聚合物非常罕见,对于无机元素来说基本上是未知的。我们报告了一种刚性和双亲核笼 (PNSiMe 3 ) 2 (NMe) 6,它具有化学稳定性并且可以从商业前体中获得数克规模,用作形成笼致密无机材料的线性和二价连接器。笼与各种双位 P(III) 二卤化物共聚单体的反应通过 Me 3 SiCl 消除进行,得到高分子量(30 000–70 000 g mol –1), 形成独立薄膜的可溶液加工聚合物。可以调整聚合物的端基以产生正交反应性并形成嵌段共聚物。可以通过使用 PCl 3作为三位基 P(III) 接头来访问网络笼状致密材料。详细的机理研究表明,在 Me 3 SiCl 损失之前,逐步缩聚通过膦-鏻离子中间体进行。因此,亲核笼和多卤化物之间的复分解代表了制造笼致密聚合物的一般策略,为系统地理解三维微观结构对宏观材料性能的影响奠定了基础。
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