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3,9-diethyl-2,4,8,10-tetraoxa-2,9-diphosphaspiro<5.5>undecane 3,9-dioxide

中文名称
——
中文别名
——
英文名称
3,9-diethyl-2,4,8,10-tetraoxa-2,9-diphosphaspiro<5.5>undecane 3,9-dioxide
英文别名
3,9-Diethyl-2,4,8,10-tetraoxa-3lambda5,9lambda5-diphosphaspiro[5.5]undecane 3,9-dioxide;3,9-diethyl-2,4,8,10-tetraoxa-3λ5,9λ5-diphosphaspiro[5.5]undecane 3,9-dioxide
3,9-diethyl-2,4,8,10-tetraoxa-2,9-diphosphaspiro<5.5>undecane 3,9-dioxide化学式
CAS
——
化学式
C9H18O6P2
mdl
——
分子量
284.186
InChiKey
HEFHCIWKUDQRIP-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):
    -0.9
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    71.1
  • 氢给体数:
    0
  • 氢受体数:
    6

反应信息

  • 作为产物:
    描述:
    3,9-diethoxy-2,4,8,10-tetraoxa-3,9-diphosphaspiro<5.5>undecane 在 溴乙烷 作用下, 反应 4.0h, 以74%的产率得到3,9-diethyl-2,4,8,10-tetraoxa-2,9-diphosphaspiro<5.5>undecane 3,9-dioxide
    参考文献:
    名称:
    Gubaidullin, R. N.; Mukmenev, E. T., Journal of general chemistry of the USSR, 1986, vol. 56, p. 2476 - 2477
    摘要:
    DOI:
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文献信息

  • Fragmentation mechanisms in mass spectrometry of Chemical Weapons Convention related spiro alkylphosphonates and alkyldioxaphosphinane oxides
    作者:Hamid Saeidian、Mehran Babri、Zohreh Mirjafary、Mohammad Taghi Naseri、Mansour Sarabadani、Davood Ashrafi、Seyyed Sajjad Mousavi Faraz
    DOI:10.1016/j.ijms.2014.06.003
    日期:2014.8
    under CWC schedule 2.B.4. Mass spectrometric studies revealed some fragmentation pathways, such as elimination of alkyl(oxo)phosphane oxide (RPO2), chlorine, chloromethylene, alkene, HCl, and H2O, α-cleavage and McLafferty-type and hydrogen rearrangements. The proposed fragmentation processes include some new fragmentation patterns, such as isomerization of cations to stabilized carbocations and oxocarbocations
    摘要 质谱图的可用性和解释技能对于明确识别与化学武器公约 (CWC) 相关的化合物至关重要。本文研究了螺烷基膦酸酯 I 和 5,5-双(氯甲基)-2-烷基-1,3,2-二氧膦烷 2-氧化物 II 作为化合物的电子电离 (EI) 和电喷雾电离 (ESI) 质谱裂解路线包含在 CWC 附表 2.B.4 中。质谱研究揭示了一些碎裂途径,例如消除烷基(氧)氧化膦 (RPO2)、氯、氯亚甲基、烯烃、HCl 和 H2O、α-裂解和 McLafferty 型以及氢重排。提议的裂解过程包括一些新的裂解模式,例如将阳离子异构化为稳定的碳正离子和氧代碳正离子,通过协同逆向[2+2]环加成反应和1,2PO烷基转移消除甲醛和烷氧基。使用 EI-MS 和 MS/MS 分析氘代类似物来确认碎片的结构。研究结果将为禁止化学武器组织(OPCW)中央分析数据库(OCAD)做出贡献,该数据库可用于在现场检查和 OPCW 能力测试期间检测和识别
  • Flame-retardant styrene type resin composition and molded product therefrom
    申请人:Yamanaka Katsuhiro
    公开号:US20070112108A1
    公开(公告)日:2007-05-17
    It is an object of the present invention to provide a styrene type resin composition excellent in thermal stability, hue, fluidity, and heat resistance, and also having the flame retardant performance, and a molded product excellent in outward appearance, formed therefrom. The present invention provides a flame retardant styrene type resin composition comprising (A) a styrene type resin (component A) in an amount of 100 parts by weight, (B) a polyphenylene ether type resin (component B) in an amount of 0 to 100 parts by weight, and (C) an organophosphorus compound (component C) represented by the following formula (1) in an amount of 1 to 100 parts by weight, characterized in that the organophosphorus compound (component C) satisfies: (i) the weight loss residue on heating at 500° C. is 10% or less; (ii) the HPLC purity is 90% or more, and (iii) the acid value is 0.5 mg KOH/g or less (where in the formula, Ar 1 and Ar 2 may be the same or different, and is a phenyl group which may have a substituent.)
  • PHOSPHORUS CONTAINING OLIGOMERS AND POLYMERS
    申请人:EMPA Eidgenoessische Materialpruefungs-und Forschungsanstalt
    公开号:US20210371591A1
    公开(公告)日:2021-12-02
    The present invention exploits reactive organophosphorus compounds containing unsaturated vinyl groups, which can be used in a flexible and highly controlled manner to prepare various macromolecular derivatives either via radical reactions or via Michael addition with suitable nucleophiles. Based on the fact that secondary amine groups on the one hand and vinyl groups on the other hand can work as mutual linking sites, an arsenal of novel and useful addition products can be built up. By selecting the number of secondary amine sites and vinyl sites of the participating reaction partners, very different addition products can be formed. In particular, one can form either linear chain type macromolecules (i.e. linear oligomers or polymers) or highly crosslinked network polymers.
  • Gubaidullin, R. N.; Mukmenev, E. T., Journal of general chemistry of the USSR, 1986, vol. 56, p. 2476 - 2477
    作者:Gubaidullin, R. N.、Mukmenev, E. T.
    DOI:——
    日期:——
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(1-氨基丁基)磷酸 顺丙烯基磷酸 除草剂BUMINAFOS 阿仑膦酸 阻燃剂 FRC-1 铵甲基膦酸盐 钠甲基乙酰基膦酸酯 钆1,5,9-三氮杂环十二烷-N,N',N''-三(亚甲基膦酸) 钆-1,4,7-三氮杂环壬烷-N,N',N''-三(亚甲基膦酸) 重氮甲基膦酸二乙酯 辛基膦酸二丁酯 辛基膦酸 辛基-膦酸二钾盐 辛-1-烯-2-基膦酸 试剂12-Azidododecylphosphonicacid 英卡膦酸 苯胺,4-乙烯基-2-(1-甲基乙基)- 苯甲基膦酸二甲酯 苯基膦酸二甲酯 苯基膦酸二仲丁酯 苯基膦酸二乙酯 苯基膦酸二乙酯 苯基磷酸二辛酯 苯基二异辛基亚磷酸酯 苯基(1H-1,2,4-三唑-1-基)甲基膦酸二乙酯 苯丁酸,b-氨基-g-苯基- 苄基膦酸苄基乙酯 苄基亚甲基二膦酸 膦酸,[(2-乙基己基)亚氨基二(亚甲基)]二,triammonium盐(9CI) 膦酸叔丁酯乙酯 膦酸单十八烷基酯钾盐 膦酸二辛酯 膦酸二(二十一烷基)酯 膦酸,辛基-,单乙基酯 膦酸,甲基-,单(2-乙基己基)酯 膦酸,甲基-,二(苯基甲基)酯 膦酸,甲基-,2-甲氧基乙基1-甲基乙基酯 膦酸,丁基乙基酯 膦酸,[苯基[(苯基甲基)氨基]甲基]-,二甲基酯 膦酸,[[羟基(苯基甲基)氨基]苯基甲基]-,二(苯基甲基)酯 膦酸,[2-(环丙基氨基)-2-羰基乙基]-,二乙基酯 膦酸,[2-(二甲基亚肼基)丙基]-,二乙基酯,(E)- 膦酸,[1-甲基-2-(苯亚氨基)乙烯基]-,二乙基酯 膦酸,[1-(乙酰基氨基)-1-甲基乙基]-(9CI) 膦酸,[(环己基氨基)苯基甲基]-,二乙基酯 膦酸,[(二乙氧基硫膦基)(二甲氨基)甲基]- 膦酸,[(2S)-2-氨基-2-苯基乙基]-,二乙基酯 膦酸,[(1Z)-2-氨基-2-(2-噻嗯基)乙烯基]-,二乙基酯 膦酸,P-[(二乙胺基)羰基]-,二乙基酯 膦酸,(氨基二环丙基甲基)-