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1,2-Propylenphosphit | 16352-26-4

中文名称
——
中文别名
——
英文名称
1,2-Propylenphosphit
英文别名
4-Methyl-2-oxido-1,3,2-dioxaphospholan-2-ium;4-methyl-2-oxido-1,3,2-dioxaphospholan-2-ium
1,2-Propylenphosphit化学式
CAS
16352-26-4
化学式
C3H7O3P
mdl
——
分子量
122.061
InChiKey
VMRLEXSQFLDWKD-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:
    56 °C(Press: 2e-2 Torr)

计算性质

  • 辛醇/水分配系数(LogP):
    -0.3
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    41.5
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:81b92d3dc957c7712dc3782316394cb6
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反应信息

  • 作为反应物:
    描述:
    1,2-Propylenphosphit1,1-二乙氧基乙烯 反应 3.0h, 以70%的产率得到2-(1,1-Diethoxy-ethyl)-4-methyl-[1,3,2]dioxaphospholane 2-oxide
    参考文献:
    名称:
    Ovchinnikov, V. V.; Cherezov, S. V.; Cherkasov, R. A., Journal of general chemistry of the USSR, 1985, vol. 55, # 5, p. 1109 - 1117
    摘要:
    DOI:
  • 作为产物:
    描述:
    1,2-丙二醇phosphorus(III) oxide 作用下, 以 2-甲基四氢呋喃 为溶剂, 反应 2.0h, 以46%的产率得到1,2-Propylenphosphit
    参考文献:
    名称:
    [EN] METHOD FOR THE SYNTHESIS OF HETEROCYCLIC HYDROGEN PHOSPHINE OXIDE
    [FR] PROCÉDÉ POUR LA SYNTHÈSE D'UN OXYDE DE D'HYDROGÉNOPHOSPHINE HÉTÉROCYCLIQUE
    摘要:
    本发明涉及一种合成杂环氢膦氧化物的方法,其具有通式(I),其中:- R是一种脂肪或芳香双价基团,可选地包含一个或多个杂原子,也可选地包含一个或多个取代基;- X和Y分别选自-O-,-C(O)O-和-NR'-,其中R'是一种可选地包含一个或多个杂原子的单价基团,包括以下步骤:a)通过混合具有通式HX-R-YH和六氧化四磷的化合物形成反应混合物;b)回收包含杂环氢膦氧化物的所得化合物。
    公开号:
    WO2016026871A1
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文献信息

  • New method of alkylene phosphonate preparation
    作者:Pawel Klosinski
    DOI:10.1016/s0040-4039(00)88906-6
    日期:1990.1
    A new method of alkylene phosphonate preparation has been elaborated, based on the reaction of the corresponding cyclic ethers and phosphonic acid in the presence of acetic anhydride.
    基于相应的环醚与膦酸在乙酸酐存在下的反应,详细阐述了一种制备亚烷基膦酸酯的新方法。
  • SYNTHESIS OF CYCLIC PHOSPHOROUS ACID ESTERS BY TRANSESTERIFICATION
    作者:Alexis A. Oswald
    DOI:10.1139/v59-220
    日期:1959.9.1
    Five- and six-membered cyclic phosphorous acid esters were synthesized by transesterification of phosphites with 1,2- and 1,3-glycols: Diethyl hydrogen phosphite was transesterified to give cyclic hydrogen phosphites. Partial transesterification of tris-2-chloroethyl phosphite resulted in cyclic 2-chloroethyl phosphites.
    五元和六元环状亚磷酸酯是通过亚磷酸酯与 1,2- 和 1,3- 二醇的酯交换反应合成的: 亚磷酸氢二乙酯被酯交换得到环状亚磷酸氢酯。亚磷酸三-2-氯乙基酯的部分酯交换产生环状亚磷酸2-氯乙基酯。
  • Novel routes to aminophosphonic acids: Interaction of dimethyl H-phosphonate with hydroxyalkyl carbamates
    作者:K. Troev、N. Koseva、G. Hägele
    DOI:10.1002/hc.20404
    日期:2008.3
    It was found that the reaction of dimethyl H-phosphonate (1) with 2-hydroxyalkyl-N-2′-hydroxyalkyl carbamates at 135°C includes several chemical reaction steps: (i) chemical transformations of 1-methyl-2-hydroxyethyl-N-2′-hydroxyethyl carbamate (2) and 2-methyl-2-hydroxyethyl-N-2′-hydroxyethyl carbamate (3); (ii) transesterification of dimethyl H-phosphonate with 2 and 3, and with secondary hydroxyl-containing
    发现 H-膦酸二甲酯 (1) 与 2-羟烷基-N-2'-羟烷基氨基甲酸酯在 135°C 的反应包括几个化学反应步骤: (i) 1-甲基-2-羟乙基- N-2'-羟乙基氨基甲酸酯(2)和2-甲基-2-羟乙基-N-2'-羟乙基氨基甲酸酯(3);(ii) H-膦酸二甲酯与 2 和 3 以及在 2-羟烷基-N-2'-羟烷基氨基甲酸酯的化学转化过程中形成的含仲羟基化合物的酯交换反应;(iii) 1 和 H-膦酸二烷基酯的水解,通过 1 与含仲羟基化合物的酯交换反应形成。通过 1H、13C、31P NMR 和 FAB 质谱法研究了相互作用。© 2008 Wiley Periodicals, Inc. 杂原子化学 19:119–124, 2008; 在线发表于 Wiley InterScience (www.interscience.wiley.com)。DOI 10.1002/hc.20404
  • Cyclic organophosphorus compounds. I. Synthesis and infrared spectral studies of cyclic hydrogen phosphites and thiophosphites
    作者:A. Zwierzak
    DOI:10.1139/v67-411
    日期:1967.11.1
    A general synthetic procedure leading to cyclic hydrogen phosphites has been devised. The effect of solvent on the P==O and P—H infrared stretching modes of cyclic hydrogen phosphites and thiophosphites has been studied. It is concluded that association of cyclic hydrogen phosphites is attributable to dipole–dipole interactions rather than to hydrogen bonding.
    已经设计了导致环状亚磷酸氢酯的一般合成程序。研究了溶剂对环状亚磷酸氢酯和硫代亚磷酸酯的 P==O 和 P-H 红外伸缩模式的影响。结论是环状亚磷酸氢盐的缔合归因于偶极-偶极相互作用而不是氢键。
  • Cyclic Phosphites of Some Aliphatic Glycols
    作者:H. J. Lucas、F. W. Mitchell、C. N. Scully
    DOI:10.1021/ja01168a032
    日期:1950.12
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同类化合物

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-(2-ethylbutoxy)-2-oxo-1,3,2-dioxaphospholane 2-(tert-butoxycarbonylamino)ethoxy-2-oxo-1,3,2-dioxaphospholane 5-dimethylamino-7-isopropylidene-8,8-dimethyl-1,4,6-trioxa-5λ5-phospha-spiro[4.4]nonan-9-one 5-dipropylaminomethyl-1,4,6,9-tetraoxa-5-phosphaspiro<4.4>nonane ethylenedioxy-O-(4,4-dimethyl-1,3-butadien-2-yl)phosphite pentamethyl-2,3,3,4,4 dioxaphospholane-1,3,2 propargyl ethylene phosphate 2-methylthio-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5-dioxaphospholane 2,2-bis(diethylamino)-2-(1,1,1,3,3,3-hexafluoro)isopropoxy-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5ς5-dioxaphospholane 4,4,5,5-tetrakis(trifluoromethyl)-2-<2,2,2-trifluoro-1-(trifluoromethyl)ethoxy>-spiro-<1,3,2λ5-dioxaphospholane-2,2'-(1,3,2λ5) dioxaphosphorinane> 4-chloromethyl-[1,3,2]dioxaphospholane 2-oxide 5-Methoxy-2,2,3,3-tetramethyl-7,9-bis(trifluoromethyl)-1,4,6-trioxa-5lambda5-phosphaspiro[4.4]non-7-en-9-ol 2,2-Dimethoxy-2-methyl-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2lambda5-dioxaphospholane 5,7-Dimethyl-2,2,3,3,9,9,10,10-octakis(trifluoromethyl)-1,4,6,8,11-pentaoxa-5lambda5,7lambda5-diphosphadispiro[4.1.47.35]tetradecane Butylamino-ethylendioxyphosphin 5-Dichloromethyl-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione 5-Fluoro-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione Ethylendioxytributylphosphoran 2-Thiono-2-t-butyl-1,3,2-dioxaphospholan (5-TB-5-13;5'-TB-5-13)-2,2,3,3,2',2',3',3'-octamethyl-5,5'-ethane-1,2-diyldioxy-bis-(1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane) (1,4-Dioxa-6,9-dithia-5λ5-phospha-spiro[4.4]non-5-yl)-dimethyl-amine 5-Trimethylsilanylmethyl-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione 5-Isopropyl-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane-2,7-dione 5-(2,2,2-Trifluoro-1-trifluoromethyl-ethoxy)-1,4,6,9-tetraoxa-5λ5-phospha-spiro[4.4]nonane 2,2,2-Tris-(2,2,2-trifluoro-1-trifluoromethyl-ethoxy)-2λ5-[1,3,2]dioxaphospholane 2,2,2-trichloro-4,4-bis-chlorocarbonylmethyl-2λ5-[1,3,2]dioxaphospholan-5-one 5,6,7,12-Tetramethyl-2,2,3,3,9,9,10,10-octakis-trifluoromethyl-1,4,8,11-tetraoxa-6,12-diaza-5λ5,7λ5-diphospha-dispiro[4.1.4.1]dodecane 2,2-Difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-Fluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane (2-TB-5-12)-2-fluoro-4,4,5,5-tetrakis-trifluoromethyl-2,2-bis-(2,2,2-trifluoro-1-trifluoromethyl-ethoxy)-2λ5-[1,3,2]dioxaphospholane Triethoxy-ethylendioxy-phosphoran 4,4,5,5-Tetrakis(trifluormethyl)-1,3,2λ5-dioxaphospholan-2,2,2-triamin 2-fluoro-4,4,5,5-tetrakis(trifluoromethyl)-1,3,2λ5-dioxaphospholane-2,2-diamine 2-Fluor-4,4,5,5-tetrakis-(trifluormethyl)-(1,3,2λ5-dioxaphospholan 5,7-difluoro-2,2,3,3,9,9,10,10-octakis-trifluoromethyl-6,12-bis-trimethylsilanyl-1,4,8,11-tetraoxa-6,12-diaza-5λ5,7λ5-diphospha-dispiro[4.1.4.1]dodecane [2-(1,1,1,3,3,3-hexamethyl-disilazan-2-yl)-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholan-2-ylidene]-trimethylsilanyl-amine 2,2-Di-tert-Butyl-2-chlor-4,4,5,5-tetrakis(trifluormethyl)-1,3,2λ5-dioxaphospholan 2-fluoro-2,2-dimethyl-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-fluoro-2,2-dimethyl-3,3,5,5-tetrakis-trifluoromethyl-2λ5-[1,4,2]dioxaphospholane 2-diethylamino-2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-diallylamino-2,2-difluoro-4,4,5,5-tetrakis-trifluoromethyl-2λ5-[1,3,2]dioxaphospholane 2-Methyl-4,4,5,5-tetrakis-trifluoromethyl-2,2-bis-(2,2,2-trifluoro-1-trifluoromethyl-ethoxy)-2λ5-[1,3,2]dioxaphospholane