10-acetoxy-decanoic acid methyl ester | 103635-69-4

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 10-acetoxy-decanoic acid methyl ester
• 英文别名: ω-Acetoxy-caprinsaeure-methylester；10-Acetoxy-decansaeure-methylester；Methyl 10-acetyloxydecanoate
• CAS: 103635-69-4
• 化学式: C₁₃H₂₄O₄
• 分子量: 244.331
• InChiKey: PZNPSRSIZCSZIL-UHFFFAOYSA-N

物化性质

• 沸点：
  287.7±8.0 °C(Predicted)
• 密度：
  0.976±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  3.2
• 重原子数：
  17
• 可旋转键数：
  12
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.85
• 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：

  10-acetoxy-decanoic acid methyl ester 生成 溶剂黄146
  参考文献：
  名称：

  Gruen; Wirth, Chemische Berichte, 1922, vol. 55, p. 2218

  摘要：

  DOI：
• 作为产物：
  描述：

  10-羟基癸酸 在 盐酸 作用下， 生成 10-acetoxy-decanoic acid methyl ester
  参考文献：
  名称：

  Gruen; Wirth, Chemische Berichte, 1922, vol. 55, p. 2218

  摘要：

  DOI：

文献信息

• Bifunctional compounds from reaction of alkoxy hydroperoxides with metal salts
  作者：G. Cardinale、J.A.M. Laan、D. Van Der Steen、J.P. Ward

  DOI：10.1016/s0040-4020(01)91447-4

  日期：1985.1

  with ferrous sulfate. C-C bond scission and radical formation was followed by dimerization of the radicals formed. Ozonides reacted similarly. Acyclic and cyclic olefins, including a cyclic enol ether, gave rise to a range of α,ω-disubstituted products in modest yields. By using ferric chloride, ω-chloro esters were obtained from the alkoxy hydroperoxides derived from olefinic esters.

  通过在醇溶液中使烯烃臭氧化而获得的氢过氧化烷氧基用硫酸亚铁处理。CC键断裂和自由基形成之后，是所形成的自由基的二聚化。臭氧反应类似。无环和环状烯烃，包括环状烯醇醚，以适度的收率产生了一系列α，ω-二取代的产物。通过使用氯化铁，从衍生自烯烃酯的烷氧基氢过氧化物获得ω-氯酸酯。
• Acetylation and formylation of alcohols with triphenylphosphine and carbon tetrabromide in ethyl acetate or ethyl formate
  作者：Hisahiro Hagiwara、Kimie Morohashi、Hitoshi Sakai、Toshio Suzuki、Masayoshi Ando

  DOI：10.1016/s0040-4020(98)00255-5

  日期：1998.5

  Alcohols were acetylated or formylated with triphenylphosphine and carbon tetrabromide in ethyl acetate or ethyl (or methyl) formate at room temperature. THP or TBDMS ether of primary alcohol got converted into formate or acetate under the experimental conditions employed in one pot operation.

  在室温下，在乙酸乙酯或甲酸乙酯（或甲基）中，用三苯膦和四溴化碳将乙醇乙酰化或甲酰化。在一锅操作中使用的实验条件下，伯醇的THP或TBDMS醚转化为甲酸酯或乙酸酯。
• Novel Preparation of α,β-Unsaturated Aldehydes. Benzeneselenolate Promotes Elimination of HBr from α-Bromoacetals
  作者：Andrei Vasil'ev、Lars Engman

  DOI：10.1021/jo9917644

  日期：2000.4.1

  elimination/hydrolysis of these mixtures afforded alpha,beta-unsaturated aldehydes in 50-80% overall yields. In the case of tertiary alpha-bromoacetals, treatment with benzeneselenolate afforded only dehydrobromination products as mixtures of isomers. The presence of at least a catalytic amount of the organoselenium reagent was found to be crucial for olefin formation. A SET-mechanism, involving benzeneselenolate-induced

  研究了乙酰化，α-溴化，亲核性苯硒基化，氧化消除/水解作为醛类α，β-脱氢的新方法。用溴在二氯甲烷中的乙缩醛处理得到相应的α-溴缩醛，产率为80-90％。然后，通过用由二苯基二硒化物，肼和碳酸钾在二甲基亚砜中原位生成的苯硒酸酯处理，可以方便地实现亲核性苯基硒烯基化。无支链的α-溴缩醛可干净地提供取代产物，而β和γ支链的则通过形式上的溴化氢损失而产生大量的α，β-不饱和缩醛。这些混合物的氧化消除/水解以50-80％的总产率提供α，β-不饱和醛。在叔α-溴缩醛的情况下，用苯硒烯酸酯处理仅得到作为异构体混合物的脱氢溴化产物。发现至少催化量的有机硒试剂的存在对于烯烃形成至关重要。提出了一种SET机制，包括苯硒酸酯诱导的电子转移到卤化物，溴离子的损失以及氢原子或质子/电子，用于苯甲酸酯促进的消除反应。旨在在分子内环化或开环反应中捕获以碳为中心的自由基的实验未能提供任何自由基中间体的证据。发现至少催化
• Molecular Healing of Polymeric Materials, Coatings, Plastics, Elastomers, Composites, Laminates, Adhesives, and Sealants by Active Enzymes
  申请人：McDaniel C. Steven

  公开号：US20100210745A1

  公开（公告）日：2010-08-19

  Disclosed herein are polymeric materials such as a coating, a plastic, a laminate, a composite, an elastomer, an adhesive, or a sealant; a surface treatment such as a textile finish or a wax; a filler for such a polymeric material or a surface treatment that includes an enzyme such as an esterase (e.g., a lipolytic enzyme, a sulfuric ester hydrolase, an organophosphorus compound degradation enzyme), an enzyme (e.g., a lysozyme, a lytic transglycosylase) that degrades a cell wall and/or a cell membrane component, a biocidal or biostatic peotide, and/or a peptidase. Also disclosed herein are methods of altering a material's property such as service life, flexability, or rigidity, by incorporation of an enzyme into a material capable of being chemically crosslinked by the activity of a lipolytic enzyme, a hydrolase, and/or a urease.

  本文公开了一些聚合材料，如涂层、塑料、层压板、复合材料、弹性体、粘合剂或密封剂；一种表面处理，如纺织品涂层或蜡；一种填料，用于这样的聚合材料或表面处理，其中包括一种酶，如酯酶（例如，脂肪水解酶，硫酸酯水解酶，有机磷化合物降解酶），降解细胞壁和/或细胞膜成分的酶（例如，溶菌酶，裂解转糖基酶），生物杀菌或生物静态肽，以及/或肽酶。本文还公开了通过将酶纳入可通过脂肪水解酶、水解酶和/或脲酶的活性交联材料中来改变材料性能，如使用寿命、柔韧性或刚度的方法。
• Anti-fouling Paints and Coatings
  申请人：Reactive Surfaces LTD

  公开号：US20150191607A1

  公开（公告）日：2015-07-09

  Disclosed herein are polymeric materials such as a coating, a plastic, a laminate, a composite, an elastomer, an adhesive, or a sealant; a surface treatment such as a textile finish or a wax; a filler for such a polymeric material or a surface treatment that includes an enzyme such as an esterase (e.g., a lipolytic enzyme, a sulfuric ester hydrolase, an organophosphorus compound degradation enzyme), an enzyme (e.g., a lysozyme, a lytic transglycosylase) that degrades a cell wall and/or a cell membrane component, a biocidal or biostatic peptide, and/or a peptidase. Also disclosed herein are methods of altering a material's property such as service life, flexability, or rigidity, by incorporation of an enzyme into a material capable of being chemically crosslinked by the activity of a lipolytic enzyme, a hydrolase, and/or a urease.

  本文披露了聚合材料，例如涂层、塑料、层压材料、复合材料、弹性体、粘合剂或密封剂；表面处理，例如纺织品整理或蜡；填充剂，用于这种聚合材料或表面处理，包括酯酶（例如脂肪水解酶、硫酸酯水解酶、有机磷化合物降解酶）的酶，降解细胞壁和/或细胞膜成分的酶（例如溶菌酶、裂解转葡糖苷酶），生物杀菌或生物稳定肽，和/或肽酶。本文还披露了通过将酶并入能够通过脂肪水解酶、水解酶和/或脲酶的活性进行化学交联的材料中，改变材料性能（例如使用寿命、柔韧性或刚度）的方法。