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1,2-bis(1,4,6,9-tetraoxa-5-phosphaspiro<4,4>non-5-yloxy)ethane | 61890-81-1

中文名称
——
中文别名
——
英文名称
1,2-bis(1,4,6,9-tetraoxa-5-phosphaspiro<4,4>non-5-yloxy)ethane
英文别名
1,2-bis(1,4,6,9-tetraoxa-5-phosphaspiro<4.4>non-5-yloxy)ethane;1,2-bis(1,4,6,9-tetraoxa-5-phosphaspiro[4,4]non-5-yloxy)ethane;5,5'-ethane-1,2-diyldioxy-bis-(1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane);5-[2-(1,4,6,9-Tetraoxa-5lambda5-phosphaspiro[4.4]nonan-5-yloxy)ethoxy]-1,4,6,9-tetraoxa-5lambda5-phosphaspiro[4.4]nonane;5-[2-(1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-5-yloxy)ethoxy]-1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonane
1,2-bis(1,4,6,9-tetraoxa-5-phosphaspiro<4,4>non-5-yloxy)ethane化学式
CAS
61890-81-1
化学式
C10H20O10P2
mdl
——
分子量
362.21
InChiKey
QSDCYZKISXVFNN-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:
    120 °C(Press: 0.05 Torr)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.7
  • 重原子数:
    22
  • 可旋转键数:
    5
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    92.3
  • 氢给体数:
    0
  • 氢受体数:
    10

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    参考文献:
    名称:
    螺旋磷光烷的形成和转化的机理—IX:螺旋磷光烷的联系反应PHaveether les ethers Vinyliques et les enamines
    摘要:
    1,4,6,9-四氧杂-5-磷(V)螺[4,4]壬烷1与乙基乙烯基醚的反应生成了一个含有PC键,5-(β-乙氧基乙基)-1的螺正膦,4,6,9-四-氧杂-5-磷(V)螺[4,4]壬烷2(自由基反应)和三配位磷化合物2-(3,5-二-氧杂-4-甲基庚烷氧基)-1,3,2-二氧戊环3(离子反应)。2,2,3,3,7,7,9-庚甲基-1,4,6-三氧九-9-氮杂-5-磷(V)螺[4,4]壬烷6仅给出含有P的螺磷烷C键,5(β-乙氧基乙基)-2,2,3,3,7,7,9-七甲基-1,4,6-三氧-9-氮杂-5-磷(V)螺[4,4]壬烷7。反应1与醇或乙二醇和烯胺一起使用时,通过氧化还原缩合反应生成五氧螺磷烷和胺。提出了这些反应的建议机制。
    DOI:
    10.1016/0040-4020(76)85141-1
点击查看最新优质反应信息

文献信息

  • Synthesis of the new adducts of imines and enamines with PH acids and their derivatives
    作者:Andrey A. Prishchenko、Mikhail V. Livantsov、Olga P. Novikova、Ludmila I. Livantsova、Elena R. Milaeva
    DOI:10.1002/hc.20513
    日期:——
    organophosphorus acids with PH fragments to various imines and enamines is proposed as convenient methods for the synthesis of new substituted aminomethyl organophosphorus compounds with three-, four-, and five-coordinated phosphorus. Also the new functionalized derivatives of these compounds with acyl and methanesulfonyl moieties are synthesized, and some properties of the obtained compounds are presented
    三价有机磷酸与 PH 片段的酯与各种亚胺和烯胺的亲核或自由基加成被认为是合成具有三、四和五配位的新型取代基甲基有机化合物的便捷方法。还合成了这些具有酰基和甲磺酰基部分的化合物的新官能化衍生物,并介绍了所得化合物的一些性质。© 2009 Wiley Periodicals, Inc. 杂原子化学 20:70–80, 2009; 在线发表于 Wiley InterScience (www.interscience.wiley.com)。DOI 10.1002/hc.20513
  • Prishchenko, A.A.; Livantsov, M.V.; Petrosyan, V.S., Russian Journal of General Chemistry, 1994, vol. 64, # 8.2, p. 1181 - 1193
    作者:Prishchenko, A.A.、Livantsov, M.V.、Petrosyan, V.S.
    DOI:——
    日期:——
  • Prishchenko, A. A.; Pisarnitskii, D. A.; Livantsov, M. V., Journal of general chemistry of the USSR, 1992, vol. 62, # 9, p. 1772 - 1773
    作者:Prishchenko, A. A.、Pisarnitskii, D. A.、Livantsov, M. V.、Petrosyan, V. S.
    DOI:——
    日期:——
  • Riesel, Lothar; Lindemann, Dirk; Ohms, Gisela, Zeitschrift fur Chemie, 1987, vol. 27, # 5, p. 181 - 182
    作者:Riesel, Lothar、Lindemann, Dirk、Ohms, Gisela
    DOI:——
    日期:——
  • FAUDET H.; BURGADA R., C. R. ACAD. SCI., 1980, C 291, NO 2, 81-83
    作者:FAUDET H.、 BURGADA R.
    DOI:——
    日期:——
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尿苷5'-二磷酸酯溴乙酰醇 N,N-二乙基-4-甲基-1,3,2-二氧杂磷杂环戊烷-2-胺 4,4,5,5-四甲基-1,3,2-二氧磷杂环戊烷-2-醇 2-氯-4-甲基-1,3,2-二氧杂磷杂环戊烷 2-氯-4,4,5,5-四甲基-1,3,2-二氧磷杂环戊烷 2-氯-1,3,2-二氧磷杂环戊烷 (3,5-二甲基苯基)[羟基(吡啶-4-基甲基)-lambda~5~-氮烷基]甲酮 2-Dipropylamino-<1,3,2 λ3>dioxaphospholan 2-ethoxy-[1,3,2]oxazaphospholidine Ethylen-2.2.2-trifluorethylphosphit-ozonid 2-dimethylamino-(3ar,9ac,3'ar',9'ac')-hexadecahydro-2λ5-[2,2']spirobi(cycloocta[1,3,2]dioxaphosphole) 2,7-dimethyl-1,4,6,9-tetraoxa-5(λ5)-phosphaspiro<4.4>nonane Aethylenselenit 4,5-bis-trifluoromethyl-2λ5-spiro[[1,3,2]dioxaphosphole-2,1'-(2,8,9-trioxa-1-phospha-adamantane)] 5,5-Difluoro-1,4,6,9-tetraoxa-5λ6-tellura-spiro[4.4]nonane N-methyl-1-(1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-5-yl)-N-(1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-5-ylmethyl)methanamine 2-methyl-5-(2,2,2-trichloroethoxy)-1,4,6,9-tetraoxa-5λ5-phosphaspiro[4.4]nonan-3-one Butan-2,3-diylselenit (4r,5t-dimethyl-[1,3,2]dioxaphospholan-2-yl)-dimethyl-amine 3,3-dibromo-2-fluoro-4-propyl-1,2λ5-oxaphosphetane 2-Fluor-2,2-dibrom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan [1,3,2]dioxaphospholan-2-yl-ethyl-amine 2-tert-butylamino-2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 3,3-dichloro-2-fluoro-4-propyl-1,2λ5-oxaphosphetane 1,1-Dibromo-3,5,8-tris-(1,1,2,2-tetrafluoro-ethyl)-2,6,7-trioxa-1λ5,4-diphospha-bicyclo[2.2.2]octane 2-Brom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan dibutyl-(4-methyl-[1,3,2]dioxaphospholan-2-yl)-amine 2-(tert-butylimino)-1,3,2,4-oxaazaphosphaboretidine 1,1,3,3,5,5,7,7-Tetrakis--tetraphosphazatetraen 2-Chlor-2,2-dibrom-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 2-Propoxy-[1,3,2]dioxaphospholan-4-one 2-Fluor-2,2-dichlor-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 2-fluoro-3-methyl-[1,3,2]oxazaphospholidine 2,2,2,4-tetrachloro-3-isopropyl-4-triflyoromethyl-1,3,2-λ5-oxazaphosphetane 1,1-Dichloro-3,5,8-tris-(1,1,2,2-tetrafluoro-ethyl)-2,6,7-trioxa-1λ5,4-diphospha-bicyclo[2.2.2]octane 2-ethoxy-2-fluoro-2λ5-[1,3,2]dioxaphospholan-2-yl phosphoric acid-(2-ethyl-2-butyl-propanediyl ester)-(2-bromo-propyl ester) (4,4-dimethyl-1,3,2-dioxaphospholan-2-yl) 2,2,2-trifluoroacetate 2-Dimethylamino-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ3-dioxaphospholan 2,3,3-Trichloro-2,2-diethyl-4-trichloromethyl-2λ5-[1,2]oxaphosphetane (5-tert-butyl-[1,3,2]dioxaphosphinan-2-yl)-dimethyl-amine 2-cyclohexyl-[1,3,2]dioxaphospholane (4-tert-Butyl-[1,3,2]dioxaphospholan-2-yl)-diethyl-amine N-Methyl-N-[1-methyl-2-(4,4,5,5-tetramethyl-[1,3,2]dioxaphospholan-2-yloxy)-propyl]-acetamide 2,2-Dichlor-2-dimethylamino-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ5-dioxaphospholan methyl-2-trioxaphosphocanne-1,3,6,2 5-dimethylamino-2,4-diisopropylidene-1,3,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane