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O,O-二异丙基(3-氯丙基)膦酸酯 | 63602-20-0

中文名称
O,O-二异丙基(3-氯丙基)膦酸酯
中文别名
——
英文名称
O,O-diisopropyl (3-chloropropyl)phosphonate
英文别名
diisopropyl (3-chloropropyl)phosphonate;diisopropyl 3-chloropropylphosphonate;(3-chloro-propyl)-phosphonic acid diisopropyl ester;(3-Chlor-propyl)-phosphonsaeure-diisopropylester;1-chloro-3-di(propan-2-yloxy)phosphorylpropane
O,O-二异丙基(3-氯丙基)膦酸酯化学式
CAS
63602-20-0
化学式
C9H20ClO3P
mdl
——
分子量
242.683
InChiKey
ZSOFQBXBNLFLSK-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

  • 熔点:
    105-106 °C
  • 沸点:
    106 °C(Press: 1.8 Torr)
  • 密度:
    1.0707 g/cm3

计算性质

  • 辛醇/水分配系数(LogP):
    2
  • 重原子数:
    14
  • 可旋转键数:
    7
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    35.5
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis, acid-base properties, and interphase distribution of new aminoalkylphosphates and -phosphonates
    作者:R. A. Cherkasov、A. R. Garifzyanov、N. S. Krasnova、M. V. Kazanova、A. V. Tarasov
    DOI:10.1134/s1070363208110078
    日期:2008.11
    Using the Todd-Atherton reaction, we synthesized new omega-aminoalkylphosphates differing by location of phosphate amino group in the molecule. For these compounds and for alpha-, beta-, and gamma-amino-phosphonates of similar structure ionization constants of phosphate and phosphonate groups were determined which turned out to be similar. In all the cases the increase in basicity of amine centers was shown with the growing distance between them and the phosphorus-containing substituent. By the method of two-phase potentiometric titration the constants of partition between water and a series of organic solvents were measured. The data obtained are interpreted in the framework of additive Leo-Hansch model that allows estimation of the increments of phosphate and amidophosphate groups. These data can be applied to the study of biological activity and extraction properties of the compound of such class.
  • Synthesis and acid-base properties of some new γ-aminophosphoryl compounds
    作者:R. A. Cherkasov、A. R. Garifzyanov、N. V. Davletshina、A. V. Tarasov、D. I. Kushnikovskii
    DOI:10.1134/s1070363212080208
    日期:2012.8
  • ——
    作者:V. S. Reznik、V. D. Akamsin、I. V. Galyametdinova
    DOI:10.1023/a:1009545706314
    日期:——
    The reactions of 3-chloropropylphosphonates, 3-chloropropylthiophosphonates, or 3-chloropropylphosphinates with 2-aryloxyethylamines or N-phenylpiperazine afford the corresponding 3-(2-aryloxyethylamino)propylphosphonates and -phosphinates or 3-(4-phenylpiperazin-1-yl)propylphosphonates and -phosphinates. The compounds obtained exhibit alpha -adrenolytic and hypotensive activities, the latter being found to depend on the substituents at the P atom.
  • Synthesis of novel mono-and bisaminophosphoryl compounds and their membrane transport properties for acidic substrates
    作者:R. A. Cherkasov、A. S. Talan、A. V. Tarasov、A. P. Garifzyanov
    DOI:10.1134/s1070363208070062
    日期:2008.7
    Some novel aminophosphoryl compounds were synthesized by the Kabachnik-Fields reaction. Their membrane transport properties for mono-and polyfunctional carboxylic acids with different number of functional groups were studied to establish that the transport rate of acidic substrates through liquid impregnated membranes increases in going from mono-to diphosphoryl carriers. Additional hydrophilic groups in the substrate molecule, too, affect transport efficiency.
  • A Study of the Reaction of Hydrocarbons with Phosphorus Trichloride and Oxygen<sup>1</sup>
    作者:A. Furman Isbell、F. T. Wadsworth
    DOI:10.1021/ja01604a025
    日期:1956.12
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同类化合物

(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)-