dimethyl decanoyl phosphonate | 118433-65-1

• 分子结构分类: 有机化合物 - 有机酸及其衍生物 - 有机膦酸及其衍生物
• 英文名称: dimethyl decanoyl phosphonate
• 英文别名: Phosphonic acid, (1-oxodecyl)-, dimethyl ester；1-dimethoxyphosphoryldecan-1-one
• CAS: 118433-65-1
• 化学式: C₁₂H₂₅O₄P
• 分子量: 264.302
• InChiKey: UDOAFUCLKOVLHL-UHFFFAOYSA-N

物化性质

• 沸点：
  320.6±25.0 °C(Predicted)
• 密度：
  1.014±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.3
• 重原子数：
  17
• 可旋转键数：
  11
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.92
• 拓扑面积：
  52.6
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  dimethyl decanoyl phosphonate 在 磺酰氯 作用下， 以 二氯甲烷 为溶剂， 反应 30.0h， 生成 ethyl 2-chloro decanoate
  参考文献：
  名称：

  Use of acylphosphonates for the synthesis of α-chlorinated carboxylic and α,α′-dichloro dicarboxylic acids and their derivatives

  摘要：

  alpha -Chloro acylphosphonates and alpha,alpha'-dichloro bisacylphosphonates were prepared in situ by chlorination of acylphosphonates and bisacylphosphonates, respectively, using sulfuryl chloride. Subsequently, they were cleaved to the corresponding alpha -chlorinated or alpha,alpha'-dichlorinated (di)carboxylic acids with a hydrogen peroxide-sodium bicarbonate system. Performing the cleavage with an alcohol or an amine yielded the corresponding alpha -chlorinated esters and alpha -chlorinated amides, respectively. (C) 2001 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0040-4020(01)00407-0
• 作为产物：
  描述：

  二甲氧基磷酰-三甲基-硅烷 生成 dimethyl decanoyl phosphonate
  参考文献：
  名称：

  GAZIZOV, T. X.;REZNIK, V. S.;MOLODYX, ZH. V.;BELYALOV, R. U.;ANISIMOVA, N+

  摘要：

  DOI：

文献信息

• Synthesis and biological evaluation of novel <i>N</i>-α-haloacylated homoserine lactones as quorum sensing modulators
  作者：Michail Syrpas、Ewout Ruysbergh、Christian V Stevens、Norbert De Kimpe、Sven Mangelinckx

  DOI：10.3762/bjoc.10.265

  日期：——

  N-alpha-haloacylated homoserine lactones, in which a halogen atom was introduced at the alpha-position of the carbonyl function of the N-acyl chain, have been studied as quorum sensing (QS) modulators and compared with a library of natural N-acylated homoserine lactones (AHLs). The series of novel analogues consists of alpha-chloro, alpha-bromo and alpha-iodo AHL analogues. Furthermore, the biological QS activity of

  已经研究了新型N-α-卤代高丝氨酸内酯，其中在N-酰基链的羰基官能团的α-位置引入了卤素原子，作为群体感应（QS）调节剂，并与天然N库进行了比较酰化的高丝氨酸内酯（AHL）。该系列新的类似物由α-氯，α-溴和α-碘的AHL类似物组成。此外，评估了与天然AHL相比，合成AHL类似物的生物学QS活性。卤代类似物在大肠杆菌JB523生物测定中显示出降低的活性，其中α-碘内酯的活性较低，而α-氯代AHL的效力最强。当在QS抑制测试中进行测试时，大多数α-卤代酰化类似物没有表现出明显的减少。所以，
• The acylphosphonate function as an activating and masking moiety for the α-chlorination of fatty acids
  作者：Christian Stevens、Laurent De Buyck、Norbert De Kimpe

  DOI：10.1016/s0040-4039(98)01939-x

  日期：1998.11

  α-Chloroacylphosphonates were prepared in situ by chlorination of acylphosphonates using sulfuryl chloride and were subsequently cleaved to the corresponding α-chlorinated fatty acids with hydrogen peroxide - sodium bicarbonate.

  通过使用硫酰氯氯化酰基膦酸酯原位制备α-氯酰基膦酸酯，随后将其用过氧化氢-碳酸氢钠裂解为相应的α-氯化脂肪酸。
• [EN] BISPHOSPHONATES AS INHIBITORS OF ACID SPHINGOMYELINASE<br/>[FR] BISPHOSPHONATES COMME INHIBITEURS DE SPHINGOMYÉLINASE ACIDE
  申请人：UNIV BERLIN HUMBOLDT

  公开号：WO2011023624A1

  公开（公告）日：2011-03-03

  The present invention refers to bisphosphonate and phosphonate/phosphate compounds of Formulae I and its use as inhibitors of aSMase enzyme activity.

  本发明涉及Formulae I的双膦酸盐和膦酸盐/磷酸盐化合物，以及其作为aSMase酶活性抑制剂的用途。
• Fungicidal activity of esters of acyl- and vinylphosphonic acids
  作者：Zh. V. Molodykh、I. A. Aleksandrova、R. U. Belyalov、T. Kh. Gazizov、V. S. Reznik

  DOI：10.1007/bf00766865

  日期：1990.2
• Enantioselective Synthesis of α-Hydroxy and α-Amino Phosphonates via Catalytic Asymmetric Hydrogenation
  作者：Mark J. Burk、Timothy A. Stammers、Judith A. Straub

  DOI：10.1021/ol9906099

  日期：1999.8.1

  [GRAPHICS]Cationic rhodium catalysts of the C-2 symmetric DuPHOS (1) and BPE (2) ligands have demonstrated the ability to asymmetrically hydrogenate a novel series of enol phosphonates (3) in good to excellent enantiomeric excess under mild conditions. Initial studies toward the catalytic asymmetric hydrogenation of enamido phosphonates (6 and 7) using the DuPHOS-Rh+ catalysts are also reported.